Stockwinners Market Radar for June 18, 2020 - Earnings, Upgrades downgrades, option trades, Best Stock Advisory Service

SRE

Hot Stocks

20:54 EDT Sempra Energy CFO sells 10.3K shares of common stock - In a regulatory filing, Sempra Energy disclosed that its CFO Trevor Mihalik sold 10.3K shares of common stock on June 18th in a transaction valued at $1.3M.
PT

Hot Stocks

20:02 EDT Pintec Technology expands cooperation with China Telecom - Pintec Technology (PT) announced that it has expanded its cooperation with China Telecom's (CHA) Bestpay, a wholly-owned subsidiary of China Telecom Corporation Limited and "one of the largest payment platforms in China", to provide handset installment services to Bestpay's government and enterprise customers. The company began working with Bestpay to expand its cooperation scope in March 2020.
CZR

Hot Stocks

19:32 EDT Caesars resumes operations at Paris Las Vegas - In accordance with directives from Nevada Governor Steve Sisolak and the Nevada Gaming Control Board, Caesars Entertainment Corporation announces that it has resumed gaming and hospitality operations at Paris Las Vegas today, June 18.
AMC

Hot Stocks

19:01 EDT AMC to reopen 450 U.S. theaters on July 15 - Beginning July 15, AMC will resume operations of 450 U.S. theatres as part of a phased plan that is expected to bring the 600-plus U.S. theatre circuit to nearly full operation leading into the opening of MULAN on July 24 and TENET on July 31. Adam Aron, CEO & President, AMC Theatres, said, "After a painful almost four-month hiatus due to the coronavirus, we are delighted to announce that movies are coming back to the big screen at AMC. Our next 100 years of making smiles happen officially begin at approximately 450 theatres across the United States on July 15. I cannot emphasize enough how much care and attention to detail we have taken in developing AMC Safe & Clean, our absolute commitment to optimizing the health and safety of our theatres for our guests and associates. Developed along with The Clorox Company, and current and former faculty of Harvard University's School of Public Health, AMC Safe & Clean represents a comprehensive commitment with a broad array of tools being used in sanitizing our theatres. Social distancing, reduced seat capacity, greatly intensified cleaning regimens, new employee health protocols, contactless ticketing and mobile food & beverage ordering are all part of AMC Safe & Clean. So too is a new multimillion-dollar commitment to implementing high tech solutions in making AMC theatres safe, including deploying electrostatic sprayers, HEPA vacuums and upgraded MERV 13 ventilation filters. All this is being put into motion because at AMC our single highest priority is the health and safety of our guests and associates. Both personally and professionally, I couldn't be more excited for what this means for movie lovers." In the coming weeks, theatre teams will begin returning to their theatres for training on AMC's new, enhanced cleaning and safety procedures. AMC expects that almost all its 600-plus U.S. locations will be open and in operation for the launch of MULAN on July 24 and TENET on July 31. The resumption of AMC operations may be adjusted if there are changes to the current theatrical release schedule, or as needed in response to local or regional conditions. To facilitate proper social distancing within theatre auditoriums, AMC will approach seat capacity limitations in four distinct phases. But AMC will always follow all federal, state and local directives, including those that mandate a maximum capacity if lower than those envisioned in AMC's four phases as now planned. The reopening schedule for specific theatres will be communicated in early July. During the weeks leading up to new major theatrical releases, AMC will be showing popular repertory titles made available from its studio partners. Those titles and ticket price information will be announced prior to reopening.
AMC

Hot Stocks

18:33 EDT AMC Entertainment CEO: We plan to open 90% of theaters on July 15 - In an interview on CNBC's Mad Money, Adam Aron said the company has plenty of cash and could stay closed until November. Once theaters are open, they will start generating cash, Aron noted. Movie theaters are not like sports stadiums. We only filled 17% of our seats in 2019, Aron said. If there is a seat limitation, we can handle it. AMC has a bright future and we'll get through the COVID-19 crisis, Aron said.
ASMB ABBV

Hot Stocks

18:01 EDT Assembly spikes over 10% after regaining worldwide rights to gastro programs - Assembly Biosciences (ASMB) is spiking over 10% or about $2.30 to $24.33 per share in after-hours trading on Thursday evening after it announced that the company will regain worldwide rights to all microbiome gastrointestinal programs licensed under its collaboration agreement with AbbVie (ABBV). ABI-M201 is currently being evaluated in a multi-center, randomized, placebo-controlled Phase 1b trial in patients with mild to moderate ulcerative colitis. ABI-M301 is a preclinical program for Crohn's disease."The company anticipates the transition to be completed in the fourth quarter of 2020. The agreement provides for a transition period of 120 days during which AbbVie will continue to fulfill its obligations under the contract. As Assembly explores strategic alternatives for the microbiome franchise, the company will continue to focus on advancing the HBV portfolio, which includes three clinical-stage core inhibitors. The company anticipates no change to its projected cash runway and that its cash, cash equivalents and investments will continue to be sufficient to fund operations into 2022. As of March 31, Assembly had cash, cash equivalents and investments totaling $249.1M.
MPC

Hot Stocks

17:58 EDT Marathon Petroleum up 5% after WSJ reports company in talks to sell Speedway - In after-hours trading, shares are up 5.74% to $40.68.
EVA

Hot Stocks

17:40 EDT Enviva lowers FY20 net income view to $33.9M-$43.9M from $52.2M-$62.2M - Raises FY20 adjusted EBITDA view to $185.0M-$195.0M from $165.0M-$175.0M. Raises FY20 distributable cash flow view to $134.0M-$144.0M from $119.0M-$129.0M, prior to any distributions attributable to incentive distribution rights paid to general partner. Now expects to distribute at least $3.00 per common unit, up from $2.87-$2.97 per unit. The company has agreed to purchase a wood pellet production plant in Waycross, Georgia with associated export terminal capacity in Savannah, Georgia from innogy SE and also has agreed to purchase the wood pellet production plant in Greenwood, South Carolina.
WEC

Hot Stocks

17:22 EDT WEC Energy recommends rejection of "mini-tender" offer from TRC Capital - WEC Energy has been notified of an unsolicited mini-tender offer by TRC Capital Investment to purchase up to 1,500,000 shares of WEC Energy Group Stock at a price of $88.88 per share in cash. TRC's offer price is approximately 4.28% lower than the WEC Energy Group common stock closing price on June 5, $92.85, and lower than today's closing price of $89.86. WEC Energy Group is not associated in any way with TRC, its mini-tender offer or the offer documentation. WEC Energy Group recommends that shareholders reject the offer and not tender their shares in response to TRC's unsolicited offer. TRC has made similar unsolicited mini-tender offers for shares of other publicly traded companies.
KRG

Hot Stocks

17:11 EDT Kite Realty Group cuts dividend to 5.2c per share from 31.75c - Kite Realty Group Trust announced that its Board of Trustees declared a quarterly cash distribution of 5.2c per common share for the quarter ending June 30. This distribution will be paid on or about July to shareholders of record as of July 2. Additionally, the company repaid $100M of the outstanding balance on its credit facility with cash on hand, thereby lowering the outstanding amount on its $600M credit facility to $200M.
AVGO

Hot Stocks

17:06 EDT Broadcom CLO sells 3,000 common shares - In a regulatory filing, Broadcom chief legal officer Mark David Brazeal disclosed the sale of 3,000 common shares of the company on June 16 at a price of $310.62 per share.
TWO

Hot Stocks

17:03 EDT Two Harbors declares 14c dividend sees Q3, Q4 dividends 'similar' - Two Harbors Investment declared a dividend of 14c per share of common stock for the second quarter of 2020. This dividend is payable on July 29 to common stockholders of record at the close of business on June 30. "The common stock dividend is a function of several factors including sustainability, earnings power of the portfolio, taxable income, impact to book value and the market environment. We believe that our portfolio is capable of generating future gross returns in the mid-double digits as we deploy capital, increase leverage and reduce expenses following non-renewal of the management agreement. As a result, we expect that our third and fourth quarter 2020 common stock dividends will be sustainable at substantially similar levels. We maintain this expectation even before giving effect to the expense savings we anticipate in the fourth quarter of 2020 following the discontinuation of management fee. As always, future dividends are dependent upon actual results and remain subject to the discretion and approval of the Board of Directors," said the company in a statement.
AL EADSY

Hot Stocks

17:01 EDT Air Lease announces delivery of new A320-200neo jet to Atlantic Airways - Air Lease Corporation (AL) announced the delivery of one new Airbus (EADSY) A320-200neo aircraft on long-term lease to Atlantic Airways, the national carrier of the Faroe Islands. Powered by CFM International LEAP-1A26 engines, this aircraft is the second of two A320-200neos that delivered to the airline from ALC's order book with Airbus. "We are pleased to announce this second A320-200neo delivery to Atlantic Airways today," said Grant Levy, Executive Vice President of Air Lease Corporation. "ALC introduced the A320-200neo to Atlantic Airways' fleet last year and it has greatly enhanced the passenger experience and overall operations of the airline. We are confident that this second A320neo from ALC will continue to support the national carrier's excellent operations."
TRUE

Hot Stocks

16:54 EDT TrueCar jumps 10% after saying vehicle demand spiked 19% from June 1-15 - Shares of TrueCar are currently up over 8% or 23c per share to 3.03 in post-market trading. The company noted in a slides presentation that that sales were recovering in May but better than anticipated.
UTL

Hot Stocks

16:46 EDT Unitil hires Robert Hevert, board anticipated to name Hevert CFO - Unitil Corporation announced the hiring of Robert B. Hevert, CFA, as Senior Vice President, effective July 23, 2020. It is anticipated that Unitil's Board of Directors will appoint Mr. Hevert to the position of Senior Vice President, Chief Financial Officer and Treasurer of the company at its upcoming meeting on July 29, 2020. It is also anticipated that Laurence M. Brock, who has served as Unitil's interim CFO and Treasurer since March 16, 2020, will step down as CFO and Treasurer on July 29, 2020, but will remain as Senior Vice President and will work directly with Mr. Hevert in order to ensure a smooth transition.
TXT

Hot Stocks

16:41 EDT Textron announces restructuring plan, headcount reductions - In a regulatory filing, Textron said, "June 18, 2020, the Board of Directors of Textron approved a restructuring plan to reduce the company's operating expenses through headcount reductions, facility consolidations and other actions in response to the economic challenges and uncertainty resulting from the COVID-19 pandemic. The restructuring plan primarily impacts the TRU Simulation + Training business within the Textron Systems segment, and the Textron Aviation and Industrial segments. At TRU, there has been a substantial decline in demand and order cancellations for flight simulators in light of the expected long-term impact of the pandemic on the commercial air transportation business. Accordingly, TRU will cease manufacturing at its Montreal, Canada facility, resulting in the production suspension of its commercial air transport simulators. As a result, we will incur charges for severance, contract terminations, facility closures, asset impairments and an inventory valuation write-down, considering the current market conditions. TRU will continue to service and support its installed base of commercial air transport simulators and to manufacture flight simulators for other fixed wing aircraft and rotorcraft at its Tampa, Florida facility. In the Textron Aviation segment, with lower volumes expected in the near term, we will initiate indirect and direct workforce reductions as we align our cost structure and production levels with demand. In the Industrial segment, the impact of the pandemic on global air travel has significantly reduced demand for the airport ground support equipment produced by the Textron Specialized Vehicles business. Due to the overall negative impact of the pandemic on this business, we will take further actions to streamline operations across TSV, consisting primarily of headcount reductions and facility rationalizations, to reduce its overall cost structure. In the second quarter of 2020, we expect to incur pre-tax special charges related to this restructuring plan in the range of $110 million to $130 million. Severance and related costs for this plan are estimated to be in the range of $60 million to $70 million. Asset impairment charges, which are largely related to facility closures, are estimated to be in the range of $30 million to $35 million, and contract termination and other facility closure charges are estimated to be in the range of $20 million to $25 million. The restructuring plan will result in the elimination of up to 1,950 positions, representing 6% of our workforce. Additionally, we will record a non-cash inventory valuation charge in the range of $50 million to $60 million. Cash outflows will occur in 2020 and are estimated to be in the range of $80 million to $95 million. We anticipate that this plan will be substantially completed by the end of 2020. During the second quarter of 2020, due to the temporary idling of manufacturing facilities as a result of the COVID-19 pandemic, we expect to incur idle facility costs in the range of $70 million to $80 million, principally in the Textron Aviation segment. In June, manufacturing operations have largely resumed across the company at these facilities as restrictions have been lifted."
SP PINC

Hot Stocks

16:41 EDT SP Plus enters into regional enhanced purchased pact with Yankee Alliance - SP Plus Corporation (SP) announced the award of an enhanced group purchasing agreement with Yankee Alliance Supply Chain Solutions, LLC and Yankee Alliance, LLC, a member-driven healthcare group purchasing organization with more than 16,800 members. Effective June 1, 2020, the new agreement designates SP+ as Yankee Alliance's preferred contracted supplier for parking and transportation operations, including parking management and planning, valet, shuttle, concierge, enforcement, facility maintenance, and patient, wheelchair and vehicle transport services. Under the agreement, participating members who enlist SP+ to provide parking and transportation services are also eligible to receive enhancements to drive additional value and savings through their aggregation philosophy. SP+ is already actively engaged in discussions related to contract activations and conversions to promote utilization of the agreement. Under this new agreement, SP+ is able to include unique value and services which are specific to the needs of Yankee Alliance members. As an affiliate of Premier, Inc. (PINC), Yankee Alliance members are also eligible to benefit from a national agreement between SP+ and Premier, which was initially executed in September 2019 as part of the SP+'s expansion of its healthcare services.
ODP ABM

Hot Stocks

16:34 EDT Office Depot announces appointment of Anthony Scaglione as CFO - Office Depot (ODP) announced the appointment of Anthony Scaglione as executive VP and CFO, effective July 20. As CFO, Scaglione will report directly to CEO Gerry Smith and be a member of the executive committee. He will be responsible for overseeing all financial aspects of the company, including financial planning and analysis, financial reporting and accounting, as well as leading investor relations, internal audit, tax, and treasury functions. Scaglione joins Office Depot from ABM (ABM) where he served as executive VP and CFO.
PBIP

Hot Stocks

16:33 EDT Prudential Bancorp approves new stock repurchase program for up to 5% - Prudential Bancorp approved the company's fourth stock repurchase program covering up to 407,000 shares or approximately 5% of its issued and outstanding shares of common stock. The company has completed its third repurchase program, repurchasing all 900,000 shares covered by the program at an average cost of approximately $13.40 per share.
OMI

Hot Stocks

16:32 EDT Owens & Minor completes sale of European logistics business, amid debt reduction - Owens & Minor announced the completion of the sale of its European logistics business, Movianto, to EHDH Holding Group, one of Europe's leading providers of healthcare logistics. "Today's divestiture enables Owens & Minor to concentrate focus on our strategic pillars - Products, Services and Distribution - and to continue expanding our PPE manufacturing capacity in the U.S. and North America," said Edward A. Pesicka, President and CEO of Owens & Minor. "This transaction also contributes to the continued financial and operational strength of Owens & Minor." In January, Owens & Minor announced its intention to sell the European logistics business, with $133M in proceeds from the sale to be used to further reduce company debt. In addition, on June 5, the company announced a tender offer for its outstanding senior notes due in 2021, to further improve long-term financial stability.
ELGX

Hot Stocks

16:31 EDT Endologix CFO Vaseem Mahboob to depart, Cindy Pinto named interim CFO - Endologix announced that Vaseem Mahboob, CFO, will be departing the company effective July 1 to become CFO of a private global healthcare company. Cindy Pinto, Vice President, Financial Planning & Analysis, will assume the role of interim CFO in addition to her current responsibilities, and the company has initiated a search process for a permanent successor that will include both internal and external candidates.
ULH

Hot Stocks

16:24 EDT Universal Logistics reports cyber-attack on network systems - In a regulatory filing, Universal Logistics announced that it experienced a cyber-attack affecting certain of the company's network systems on June 8. "During the attack, the company experienced limited disruption and rapidly deployed back-up systems or implemented temporary procedures to maintain operations. The company is investigating the attack, including the scope of transferred or extracted data," the filing stated.
HST

Hot Stocks

16:22 EDT Host Hotels recommends shareholders reject "mini-tender" offer by Mackenzie - Host Hotels has learned that MacKenzie Capital Management made an unsolicited "mini-tender" offer for up to 90,000 operating partnership units of Host Hotels at a price of $8.55 per OP Unit less cash distributions made by Host L.P. after May 31. This follows multiple earlier "mini-tender" offers by the Purchaser launched between 2016 and 2019. Neither the Company nor Host L.P. are in any way associated with the MacKenzie Offer, and holders of OP Units are under no obligation to take any action with respect to the MacKenzie Offer. The company and Host L.P. recommend that the holders of OP Units reject this unsolicited offer, since the offer price is below the $12.31 per share closing stock price of the company's common stock on June 17. An OP Unitholder would receive shares with a market value of approximately $12.57 compared to the cash MacKenzie Offer of $8.55.
PCG

Hot Stocks

16:22 EDT PG&E accepts sentence in Butte County court related to role in 2018 Camp Fire - PG&E accepted its sentence in Butte County Superior Court related to the company's role in the 2018 Camp Fire. In accordance with the plea agreement PG&E reached in March 2020 with the Butte County District Attorney, the company pleaded guilty to 84 counts of involuntary manslaughter and one count of unlawfully starting a fire. The following statement was delivered today in court by incoming Interim CEO of PG&E Corporation Bill Smith: "During these past two days, we have heard the victims of the 2018 Camp Fire share their traumatic and tragic experiences. We have heard every word-from the ones in person, the ones on the phone and the ones read by Mr. Ramsey. We respect and honor each of those victims-what they have experienced and what they have shared with us at this hearing. We will never forget their pain. It can never be said too many times: We accept responsibility for our role in the Camp Fire, and all 23,000 employees are committed to making sure our equipment never again causes a catastrophe like this. On behalf of everyone at PG&E, I'm truly sorry for the terrible loss of life and the physical and emotional damage resulting from the fire. I recognize that no apology, no plea, no sentencing can undo that damage, and no passage of time can lessen the anguish we heard expressed in this courtroom. All of us know that actions speak louder than words. We have taken action, and we will continue to take action to combat the growing threat of wildfires and keep our customers and our communities safe. We have been working tirelessly to improve our processes, harden our systems, and incorporate advanced weather technology to give us better insight into what's happening in these risky conditions. Overall, we are making comprehensive and meaningful changes to make PG&E the safe and reliable utility that Northern and Central Californians deserve. We are committed fully to continuing that work. While nothing will repair the wounds caused by the Camp Fire, we hope the actions we are taking will begin to restore the trust of our communities and their confidence that we are working to keep them safe. Your Honor, we have come before this Court, the Camp Fire victims, and the community-with humility and respect-ready to be held to account for this tragedy and committed to regaining the trust that we have broken."
CLR

Hot Stocks

16:18 EDT Continental Resources to partially begin resuming production in July - Continental Resources announced an update on its voluntary production curtailments. The company previously announced it would curtail 70% of operated oil production in May, with continued curtailments into June. In July, the company expects to partially begin resuming production but still expects to curtail approximately 50% of its operated oil production. June total production is expected to average 150,000 to 160,000 Boepd. Second quarter total production is expected to average 200,000 to 205,000 Boepd. July total production is expected to average 225,000 to 250,000 Boepd. "Continental elected to defer production in order to preserve shareholder value over volumes, and maximize the economics of the barrels we produce. As oil prices have stabilized and begun to recover, we have partially resumed production. As improved supply and demand fundamentals benefit oil prices, we expect to continue restoring production in subsequent months," said Bill Berry, CEO.
SGA

Hot Stocks

16:16 EDT Saga Communications temporarily suspends quarterly dividend - Saga Communications announced that its Board of Directors is temporarily suspending the quarterly cash dividend in response to the continued economic uncertainty of the impact of COVID-19. Additional actions being taken to conserve the company's cash position include reducing planned capital spending and seeking discounts from vendors. By preserving the company's cash position, the company believes market conditions may present attractive acquisition opportunities. The company will consider the resumption of quarterly cash dividends in the near future as economic conditions permit.
MEI

Hot Stocks

16:10 EDT Methode Electronics declares 11c quarterly dividend - Methode Electronics announced toay that its board of directors has declared a quarterly dividend of 11c per share to be paid on July 31 to common stockholders of record at the close of business on July 17.
DDOG

Hot Stocks

16:10 EDT Datadog achieves FedRAMP low-impact SaaS authorization - Datadog announced it has achieved FedRAMP authorization for low-impact SaaS. Datadog is fully available in the FedRAMP marketplace as of May 14, 2020. Achieving FedRAMP authorization allows U.S. federal government departments and agencies to adopt and use Datadog's cloud platform.
MGEN

Hot Stocks

16:09 EDT Miragen Therapeutics appoints Lee Rauch as COO - Miragen Therapeutics announced the appointment of Lee Rauch as COO, effective immediately. Rauch reports directly to president and CEO William Marshall and is responsible for overseeing Miragen business development, licensing, partnerships, investor relations, corporate communications, intellectual property and new product planning. Rauch has more than 25 years of experience in the biotech and pharmaceutical industries, helping build companies from pre-clinical stage to advanced clinical development. Prior to joining Miragen, she was the executive in residence at Columbia Technology Ventures.
BA ADM

Hot Stocks

16:09 EDT Boeing names Michael D'Ambrose as EVP of Human Resources - Boeing (BA) named Michael D'Ambrose as executive vice president of Human Resources, effective July 6. He will succeed Wendy Livingston, who has served in an interim capacity since April. D'Ambrose joins Boeing from Archer-Daniels-Midland (ADM). He has served as senior vice president and chief human resources officer at ADM since 2006.
GCI

Hot Stocks

16:08 EDT Gannett eliminates Gannett Media CEO position - Gannett announced that the board has decided to streamline the operating structure of the company by eliminating the position of CEO of the operating company, Gannett Media Corp. Given this decision, the board and Paul Bascobert have mutually agreed for Mr. Bascobert to terminate his employment with the company. Mr. Bascobert's departure is not the result of any inappropriate action by Mr. Bascobert, any violation of company policy, any accounting irregularity or any material deterioration in the business of the company.
ASMB ABBV

Hot Stocks

16:08 EDT Assembly Biosciences says AbbVie terminating gastrointestinal pacts - Assembly Biosciences (ASMB) announced that the company will regain worldwide rights to all microbiome gastrointestinal programs licensed under its collaboration agreement with AbbVie (ABBV). AbbVie has decided to terminate the research, development, collaboration and license agreement. This decision was not based on any efficacy, safety, or other data related to the collaboration programs. "We are grateful for the opportunity to work collaboratively on the development of our microbiome gastrointestinal programs. Together, we were able to advance ABI-M201 into the clinic to evaluate this novel biotherapeutic in patients with ulcerative colitis. With the return of all rights to the program, we have now begun to explore a broader set of strategic alternatives to continue development of these programs," said John McHutchison, AO, MD, Chief Executive Officer and President of Assembly. ..The Company anticipates the transition to be completed in the fourth quarter of 2020. The agreement provides for a transition period of 120 days during which AbbVie will continue to fulfill its obligations under the contract. As Assembly explores strategic alternatives for the microbiome franchise, the Company will continue to focus on advancing the HBV portfolio, which includes three clinical-stage core inhibitors The Company anticipates no change to its projected cash runway and that its cash, cash equivalents and investments will continue to be sufficient to fund operations into 2022. As of March 31, 2020, Assembly had cash, cash equivalents and investments totaling $249.1 million.
MYL BIIB

Hot Stocks

16:07 EDT Mylan wins District Court decision against Biogen's Tecfidera patent - Mylan (MYL) announced that the U.S. District Court for the Northern District of West Virginia invalidated Biogen's (BIIB) Tecfidera patent, U.S. Patent No. 8,399,514, for lack of written description. The 514 patent claimed methods of treating multiple sclerosis using a dose of 480 mg/day of dimethyl fumarate delayed release capsules. Today's decision clears the way for Mylan's launch of its dimethyl fumarate product upon the receipt of FDA approval. The '514 patent could have otherwise delayed generic competition until 2028. Mylan CEO Heather Bresch commented: "Today's win is significant in that it brings Mylan one step closer to providing expanded treatment options for the thousands of Americans living with relapsing forms of MS. The District Court decision clears the legal pathway for us to bring our dimethyl fumarate product to market, and we are working with the FDA to accelerate our regulatory approval target action date, which currently is November 16. Once approved and launched, we believe our generic Tecfidera will potentially be the first generic of any MS treatment in an oral solid dosage form available to patients in the U.S., further advancing our commitment to provide a broad portfolio of central nervous system medicines, which already includes glatiramer acetate injection." Biogen's total IQVIA sales in the U.S. for the 12 months ending April 30, 2020, were approximately $3.78B for Tecfidera.
SLM

Hot Stocks

16:06 EDT Sallie Mae names Carter Warren Franke as Chair of the board - Sallie Mae announced that Carter Warren Franke has been appointed Chair of its Board of Directors, effective immediately. Ms. Franke is the first woman to lead the company's board. Ms. Franke has served as an independent director and member of Sallie Mae's Board since April 2014.
AKBA

Hot Stocks

16:04 EDT Akebia appoints David Spellman as CFO - Akebia appointed David A. Spellman as its new Senior VP, CFO and Treasurer, effective June 29. Spellman will join Akebia from Intarcia Therapeutics, where he is CFO and Chief Business Officer. Spellman will succeed Jason Amello, who has served as Senior VP, CFO and Treasurer since 2013. Although Amello is stepping down from the position to pursue other professional interests, he will remain with Akebia for a period of time to ensure a smooth transition of responsibilities to Spellman and will continue to advise the company as a consultant thereafter. Prior to joining Intarcia, Spellman served as CFO of Mersana Therapeutics, a clinical stage antibody drug conjugate company. From February 2006 to March 2018, Spellman served in a series of roles at Vertex Pharmaceuticals.
HTGM

Hot Stocks

16:03 EDT HTG Molecular Introduces the HTG EdgeSeq Pan B-Cell Lymphoma Panel - HTG Molecular Diagnostics announced the pre-launch introduction of its new HTG EdgeSeq Pan B-Cell Lymphoma Panel, which is expected to be commercially available for purchase in kit form or as a service in HTG's VERI/O laboratory starting in July 2020. The HTG EdgeSeq Pan B-Cell Lymphoma Panel is a research-use only panel designed to provide molecular characterization of aggressive lymphomas by allowing researchers to measure the expression of genes associated with the aggressive lymphoma transcriptome. Globally, there are nearly 600,000 new cases of lymphoma diagnosed and over 250,000 deaths from the various lymphoma subtypes annually. Correctly diagnosing lymphomas often requires 20 or more immunohistochemical tests, and incorrect subtype classification is common. HTG's new comprehensive HTG EdgeSeq Pan B-Cell Lymphoma Panel is designed to better facilitate identification of lymphoma subgroups addressing this important market.
UIHC

Hot Stocks

16:03 EDT United Insurance names R. Daniel Peed as CEO effective July 1st - United Insurance announced its board has appointed R. Daniel Peed as Chairman of the board and CEO, effective July 1, 2020. Most recently Mr. Peed was Vice Chairman of the company's Board of Directors. Greg Branch, who has served as Chairman of the Board since the Company's founding in 1999, will remain a member of the Board of Directors and assume the title of Chairman Emeritus effective the same date. Mr. Peed will succeed John L. Forney, who will be stepping down as President and CEO, effective June 30, 2020, to pursue other opportunities.
FB GOOG

Hot Stocks

15:37 EDT Facebook has acquired map data firm Mapillary - "Today we're announcing that Mapillary has joined Facebook (FB) on the quest to improve maps everywhere and for everyone.From day one of Mapillary, we have been committed to building a global street-level imagery platform that allows everyone to get the imagery and data they need to make better maps. With tens of thousands of contributors to our platform and with maps being improved with Mapillary data every single day, we're now taking the next big step on that journey. Today, we're excited to share that Mapillary has joined Facebook to be part of their open mapping efforts. As some of you know, Facebook is building tools and technology to improve maps through a combination of machine learning, satellite imagery and partnerships with mapping communities, as part of their mission to bring the world closer together. These maps power products like Facebook Marketplace that drive transactions for millions of small businesses, and supply vital data to humanitarian organizations around the world," said the company in a blog posting. The Fly notes that Google (GOOG) operates a mapping service also called Google Maps. Reference Link
HTZ

Hot Stocks

15:26 EDT Hertz trading resumes
GOOG GOOGL

Hot Stocks

15:18 EDT Google's workshop for experimental products, Area 120 launches Keen - "Have things you're passionate about and want more of? Keen helps you expand your interests and connect them with other people," says the Keen team. Reference Link
HTZ

Hot Stocks

15:16 EDT Hertz terminates plans for 'at the market' offering of up to $500M of stock - In a regulatory filing, Hertz stated: "As previously disclosed, on June 12, 2020, the United States Bankruptcy Court for the District of Delaware granted the motion of Hertz Global Holdings for authority to enter into an Offer and Sale Agreement and to sell shares of its common stock, par value $0.01 per share. Also as previously disclosed, the company commenced an "at the market" offering of up to $500M of its common stock after the filing on June 15, 2020, of a prospectus supplement under its effective shelf registration statement on Form S-3, dubbed the "ATM Program." In the afternoon on June 15, 2020, the Staff of the Securities and Exchange Commission's Division of Corporation Finance verbally notified the company that the Staff was reviewing the prospectus supplement. Promptly thereafter, the company suspended all sales of common stock under the ATM Program. Effective June 18, 2020, the Finance Committee of the Board of Directors determined that it was in the best interests of the company to terminate the ATM Program and directed that the ATM Program be terminated."
AEMD

Hot Stocks

15:02 EDT Aethlon Medical spikes over 90% after FDA approves IDE supplement for Covid-19 - Shares of Aethlon Medical are currently up approximately 90% or $1.25 to $2.66 per share in afternoon trading after the company announced that the U.S. FDA has approved a supplement to the company's existing Investigational Device Exemption for the company's Hemopurifier in viral disease to allow for the testing of the Hemopurifier in patients with SARS-CoV-2/COVID-19 in a new feasibility study.
IMAX...

Hot Stocks

14:51 EDT Imax announces documentary film streaming deal with Hulu - IMAX Corporation (IMAX) announced that several titles from its catalog of documentary films will be available to stream exclusively on Hulu in the U.S. beginning this summer, kicking off with "A Beautiful Planet," "Pandas," and more. In total, at least 16 IMAX documentaries will roll out on Hulu over the next several weeks and months. Additional terms of the agreement were not disclosed. Hulu is majority-owned by Disney (DIS) with Comcast (CMCSA) a minority partner.
AMZN

Hot Stocks

14:35 EDT TwitchCon San Diego canceled amid COVID-19 concerns - TwitchCon, a biannual convention for Amazon's live streaming platform Twitch, said via Twitter: "In March, we made the incredibly difficult decision to cancel TwitchCon Amsterdam. Over the past few months, we have continued to closely monitor the COVID-19 pandemic with TwitchCon San Diego weighing on our minds. Due to restrictions on large gatherings and ongoing concerns for the healthy and safety of our community, the Twitch team, and the local San Diego community, we have decided to cancel TwitchCon San Diego this fall. We are gutted that we won't be able to see all of you in person to connect and show you what we've been creating for you over the past year. While we can't gather in person, we're exploring ways that we could join forces in an alternate dimension later this year. We'll keep you posted." The event had been previously scheduled for September 25-27. Reference Link
OTGLY...

Hot Stocks

13:53 EDT CD Projekt delays 'Cyberpunk 2077' release to November 19 - CD Projekt (OTGLY) has delayed the release of its upcoming game "Cyberpunk 2077" to November 19 from September 17. "At the time we are writing these words, Cyberpunk 2077 is finished both content and gameplay-wise," the company said in a statement posted on Twitter. "The quests, the cutscenes, the skills and items; all the adventures Night City has to offer -- it's all there. But with such an abundance of content and complex systems interweaving with each other, we need to properly go through everything, balance game mechanics and fix a lot of bugs. A huge world means a huge number of things to iron out and we will spend the additional time doing exactly that." The game is set to come out on PC, Stadia (GOOG), PlayStation 4 (SNE), Xbox One (MSFT), and Xbox Series X. Reference Link
DFLYF

Hot Stocks

13:44 EDT Draganfly announces election of John Mitnick to board of directors - Draganfly announces that John Mitnick, former General Counsel of the U.S. Department of Homeland Security and Raytheon senior executive, was elected to the company's board of directors at the company's annual general meeting on June 18. Since November 2019, Mitnick has served as a consultant to the company advising on government and commercial business opportunities. Mr. Mitnick said: "Having worked with the talented Draganfly team since last November, it is clear that the company is a technology and innovation leader in the unmanned aerial vehicle industry with a sophisticated vision for growth. I am looking forward to contributing to the achievement of that vision in this new role."
LVGO

Hot Stocks

13:38 EDT Livongo studies show remote technologies can utilize data insights for diabetes - Livongo Health announced the findings of two studies that demonstrate how remote monitoring technologies can utilize continuous and unique data insights via its AI+AI engine to better inform care decisions and outcomes. The research findings were presented at the American Diabetes Association's 80th Scientific Sessions: A Virtual Experience held on June 12-16. The first study, Predictors of Emergency Department and Inpatient Admissions after Hypo- and Hyperglycemic Events: Leveraging Remote Monitoring Data of People with Diabetes, included 7,633 study participants and used Livongo's cellular-enabled blood glucose monitor and remote monitoring capabilities to determine specific predictors which may lead to a hypoglycemic or hyperglycemic event. The study determined that a gap in days between checking, more 'Missed Medication' tags, fewer 'Before Breakfast' tags, new users of oral diabetes medications, and other factors were predictors associated with future emergency department and inpatient visits due to a hypoglycemic event. It also found that models pairing blood glucose values with rich data including time of day, meal tags, medication use, and feeling tags are more likely to predict those who are at a higher-risk of costly care interventions than models using blood glucose data alone. The second study, Is Activation, Behaviors, and Attitudes to Managing Care Associated with Utilization of a Remote Diabetes Monitoring Platform (RDMP) and Improvement of A1c, was conducted in collaboration with Eli Lilly & Company and included 1,089 participants. The study found a direct correlation between improvements in Diabetes Empowerment Scale-Short Form (DES-SF) and increased platform utilization. In addition, participants who used the Livongo platform more regularly and those who achieved measurable improvements in Diabetes Distress Scale 17 (DDS17) experienced better glycemic control. "Through Livongo's ability to collect a breadth of real-time data points, including meal tags and feeling tags, we are able to build out comprehensive Member profiles and direct interventions and features from our platform that lead to improved clinical outcomes," said Dr. Bimal Shah, Chief Medical Officer of Livongo and senior author of the studies. "As Livongo's AI+AI engine aggregates more data, our platform continues to improve by providing a more personalized care experience. We are able to leverage a combination of machine learning and clinical studies to continue to improve outcomes, drive down health care costs, improve utilization, and empower people to better manage their diabetes."
EPZM

Hot Stocks

13:32 EDT Epizyme receives accelerated approval for Tazverik for two FL indications - Epizyme announced that the U.S. Food and Drug Administration has approved the supplemental New Drug Application for TAZVERIK for the following two distinct follicular lymphoma indications: Adult patients with relapsed or refractory FL whose tumors are positive for an EZH2 mutation as detected by an FDA-approved test and who have received at least two prior systemic therapies. Adult patients with relapsed or refractory FL who have no satisfactory alternative treatment options. These indications were approved under accelerated approval with a priority review, based on overall response rate and duration of response in the company's Phase 2 clinical trial cohorts of FL patients with EZH2 mutations and wild-type EZH2. TAZVERIK received initial accelerated approval by FDA on January 23, 2020 for the treatment of adult and pediatric patients aged 16 years and older with metastatic or locally advanced epithelioid sarcoma not eligible for complete resection. "We are very pleased to be able to offer TAZVERIK as a treatment option for relapsed or refractory FL patients, which is the culmination of many years of work by our team," said Dr. Shefali Agarwal, chief medical officer of Epizyme. "In our view, there remains no clear standard of care in the relapsed and/or refractory FL population as not all patients benefit from today's available therapies. Based on this label, physicians will have the ability to use their clinical discretion to prescribe TAZVERIK for their relapsed or refractory patients regardless of EZH2 mutational status and without regard to a specific line of treatment where other options are not satisfactory. We are grateful to the many patients, physicians and medical teams who helped bring us to this important achievement."
SGMS

Hot Stocks

13:26 EDT Scientific Games expands sports betting partnership with Betfred - Scientific Games Corporation expanded its sports betting partnership with Betfred to roll out its digital and retail solutions in the state of Colorado. Following Betfred's selection of Scientific Games to provide OpenSports in Pennsylvania earlier this year, the two companies have now extended their collaboration to include digital and retail sportsbook services at the Saratoga Casino Black Hawk in Colorado. Betfred has now launched OpenSports full retail solutions including Self-Service Betting Terminals at Saratoga Casino Black Hawk, with the Company's Digital services expected to follow in time for the 2020-2021 NFL season. In addition, Scientific Games will supply Betfred's operations in Colorado with OpenPlatform.
RARE

Hot Stocks

13:19 EDT Ultragenyx, Kyowa Kirin announce FDA approves second indication for Crysvita - Ultragenyx Pharmaceutical (RARE) and Kyowa Kirin Co. announced that the U.S. Food and Drug Administration has approved Crysvita for the treatment of fibroblast growth factor 23-related hypophosphatemia in tumor-induced osteomalacia, or TIO, associated with phosphaturic mesenchymal tumors that cannot be curatively resected or localized in adults and pediatric patients 2 years of age and older. Crysvita is a human antibody that blocks excess activity of FGF23, a hormone that causes phosphate urinary excretion and suppresses active vitamin D production by the kidney. This is the second FDA-approved indication for Crysvita, which was first approved in April 2018 for the treatment of X-linked hypophosphatemia in adult and pediatric patients one year of age and older. The XLH indication was expanded in September 2019 to include infants as young as six months of age.
AESE

Hot Stocks

13:11 EDT Allied Esports pops almost 30% after its Las Vegas reopen plan - Shares of Allied Esports are currently up 27.5% or 58c to $2.66 per share in afternoon trading on Thursday after the company said its flagship venue, HyperX Esports Arena Las Vegas, located at Luxor Hotel & Casino, will reopen to the public on Thursday, June 25 with a modified schedule for daily play and weekly tournaments. "The health of our communities will always come first and foremost, and we've taken the necessary steps to create an environment where gamers can come together again," said Jud Hannigan, CEO of Allied Esports. "We're confident that with our safety protocols in place players and fans will still be able to enjoy the thrill of the on-site experience that HyperX Esports Arena is known for."
PINC

Hot Stocks

13:03 EDT Premier announces oncology-focused purchasing alliance for branded cancer drugs - Premier announced the debut of Intersectta, a new oncology-focused group purchasing organization, or GPO, to source cancer and other specialty drugs. "Through this program, Premier plans to strike innovative new partnerships with pharmaceutical companies, putting branded products on negotiated contracts at competitive prices. In addition, Premier will provide participants access to robust market data to better understand real-world prescribing, utilization and off-label trends. Guided by an Advisory Committee composed of 20 of the nation's largest and most prestigious health system providers representing more than 385 individual hospitals providing care to nearly 8 million patients living with cancer, Intersectta will initially focus on a targeted pipeline of nearly 70 oncology drugs that are most commonly used in cancer care," the company stated.
JLL

Hot Stocks

13:03 EDT JLL 'on track' to reopen nealy 100 U.S. offices by end of July - JLL has re-opened more than 75 offices in the United States, a little more than half of its total portfolio, including its flagship headquarters at the Aon Center in Chicago. The company is on track to re-open nearly 100 U.S. offices by the end of July. The re-openings follow the company's moves outside the U.S., where most of its facilities have welcomed employees back in partial capacity over the past few months. JLL employs more than 94,000 people across 80 countries and, to date, has opened 84 offices in Asia Pacific and 78 offices in EMEA. The firm is utilizing learnings from those regions as it continues its re-entry in the U.S. Consistent with its advice to clients, JLL is implementing shifts to reduce the number of employees in the office at one time. For example, at Aon Center the firm is bringing back no more than 25% of employees during Phase 1, which is also in compliance with both city and state restrictions. JLL is implementing a phased approach to re-entry that emphasizes employee health and safety as its top priorities. Revised space plans to promote social distancing, signage that outlines safe hygiene practices, rotational shifts, cleaning protocols and distribution of cloth face coverings to employees are some of the practices in place.
RDHL

Hot Stocks

13:01 EDT RedHill expands opaganib COVID-19 phase 2/3 study in Italy, U.K. - RedHill Biopharma Ltd. announced that it has submitted Clinical Trial Applications with the UK Medicines & Healthcare Products Regulatory Agency and the Italian Medicines Agency for a Phase 2/3 clinical study evaluating opaganib in patients hospitalized with severe SARS-CoV-2 infection, the cause of COVID-19, and pneumonia. Mark L. Levitt, M.D., Ph.D., Medical Director at RedHill, said: "We are quickly advancing the preparations for a global, multi-center powered Phase 2/3 study with opaganib for COVID-19. In line with the global shift from a focus on compassionate use programs to adequately controlled clinical studies, our highest priority is on generating robust data in a controlled setting for regulatory purposes. Following our submission of the Clinical Trial Application in Russia last week, we have submitted similar applications in the UK and Italy, and we are looking to expand the study to additional countries and start treating patients soon. This study, along with the ongoing Phase 2a study in the U.S., should allow us to enroll patients faster to evaluate the efficacy of opaganib against COVID-19 and bring this promising therapy one step closer to those who need it." The multi-center, randomized, double-blind, parallel-arm, placebo-controlled Phase 2/3 study is planned to enroll up to 270 subjects with severe COVID-19 pneumonia requiring hospitalization and treatment with supplemental oxygen. Subjects will be randomized at a 1:1 ratio to receive either opaganib or placebo, on top of standard-of-care therapy. The primary endpoint of the study is to evaluate the proportion of patients requiring intubation and mechanical ventilation by Day 14. An unblinded futility interim analysis will be conducted when approximately 100 subjects have been evaluated for the primary endpoint.
HTZ

Hot Stocks

12:49 EDT Hertz shares down 5% to $1.90 prior to halt for news
HTZ

Hot Stocks

12:47 EDT Hertz trading halted, news pending
CHH

Hot Stocks

12:08 EDT Choice Hotels: WoodSpring Suites experienced 70% occupancy rate in May - Choice Hotels says in a statement that its extended stay portfolio - led by WoodSpring Suites - outperformed the overall industry in several ways over the past three months, including: For the month of March, Choice Hotels' extended stay brands achieved an average occupancy level of over 68%, compared to the U.S. hotel industry average of approximately 40%. In April, the company's extended stay portfolio attained a 60% occupancy level, which more than doubled the industry average of 25%. Choice's extended stay brands continued their impressive performance in May with an average occupancy of 67%. Specifically, the WoodSpring Suites brand achieved an average occupancy rate of over 70% in the month of May, making it one of the best-performing brands in the hotel industry in recent months. Despite an industrywide RevPAR decline of nearly 52% in March and 80% in April, Choice says RevPAR for all of its extended stay brands declined less than 14% and 29%, respectively.
LRLCY

Hot Stocks

12:08 EDT L'Oreal acquires skincare brand Thayers Natural Remedies - L'Oreal announced the signing of an agreement to acquire Thayers Natural Remedies,a U.S.-based natural skincare brand from Henry Thayer Company. The brand will be integrated into L'Oreal's Consumer Products Division. Thayers recorded sales of $44M in 2019.
MCD

Hot Stocks

12:05 EDT McDonald's Restaurants expect to hire about 260,000 workers this summer - As states and communities continue to re-open their economies, McDonald's restaurants are expecting to hire approximately 260,000 restaurant employees this summer. This comes as McDonald's restaurants begin to welcome customers back into dining rooms with extra precautions in place, the company said. McDonald's has implemented nearly 50 new safety procedures to protect crew and customers. These include wellness and temperature checks, social distancing floor stickers, protective barriers at order points, masks and gloves for employees with the addition of new procedures, and training for the opening of dining rooms. "We are excited to welcome new employees to our McFamily, and we want candidates and their families to know we have one goal - to keep our people safe. We've put new minimum national standards and nearly 50 new processes in place in our restaurants as they continue to re-open safely and judiciously," said Joe Erlinger, President of McDonald's USA. "Our local business owners are proud to help their communities and provide employment and educational opportunities to hundreds of thousands of people this summer." Reference Link
DLNG

Hot Stocks

12:00 EDT Dynagas LNG rises 12.7% - Dynagas LNG is up 12.7%, or 40c to $3.52.
COE

Hot Stocks

12:00 EDT China Online Education rises 13.0% - China Online Education is up 13.0%, or $2.73 to $23.75.
ABM

Hot Stocks

12:00 EDT ABM rises 14.2% - ABM is up 14.2%, or $4.61 to $37.14.
WU AXAHY

Hot Stocks

11:58 EDT Western Union partners with AXA over insurance services - Western Union (WU) announced a new strategic partnership with AXA (AXAHY) to leverage Western Union's global omni-channel platform to deliver affordable life and disability insurance offerings to consumers in France, sending money via www.westernunion.com to 10 African countries. The partnership will initially be a pilot program which Western Union and AXA hope to grow and scale over time. "This partnership shows the power of our global cross-border, cross-currency payments platform," said Western Union CEO Hikmet Ersek. "Our long-term goal is to leverage our platform and digital capabilities to forge more partnerships and become a financial services ecosystem. In enabling third parties, including banks and other financial institutions, to tap into our ecosystem capabilities, these companies can offer similar services for their customers. We are pleased to offer insurance services in collaboration with AXA to serve our customers and their families who both know and trust Western Union."
SPOT T

Hot Stocks

11:55 EDT Spotify, Warner Bros. partner to over DC superhero podcast content - Spotify (SPOT) is entering into a new multiyear partnership with Warner Bros. (T) and DC to produce and distribute an original slate of narrative scripted podcasts exclusively on Spotify. The partnership-the first to involve the intellectual property of the entire DC Universe -will leverage iconic characters in new Spotify shows. Additionally, the companies are expected to draw upon Warner Bros. Studio's broader collection of titles as stand-alone podcast series. Warner Bros. Digital Networks will manage the business and strategy related to the partnership. Warner Bros. Television Group's digital studio, Blue Ribbon Content, will oversee the creative relationship and will co-develop and produce the programming in collaboration with Spotify, which will be responsible for the marketing, advertising, and distribution of the shows exclusively on its platform. The news comes after the Wall Street Journal reported yesterday that Spotify has reached a deal with Kim Kardashian West for a podcast about her involvement with the Innocence Project. Shares of Spotify are up roughly 11% near noon.
BIIB

Hot Stocks

11:52 EDT Biogen to appeal court decision that Tecfidera patent invalid - In a regulatory filing, Biogen (BIIB) confirmed that on June 18, 2020, the U.S. District Court for the Northern District of West Virginia issued a decision finding the asserted claims of the company's U.S. patent No. 8,399,514, which claims the Tecfidera daily dosing regimen of 480 mg/day of dimethyl fumarate to treat multiple sclerosis, to be invalid. "Biogen intends to appeal this decision," the filing stated.
LIFE

Hot Stocks

11:43 EDT aTyr Pharma highlights research implicating neuropilin pathway in COVID-19 - Last night, aTyr Pharma highlighted new external research that it said demonstrates the involvement of Neuropilin biology in SARS-CoV-2 infection. The company noted that it is currently investigating Neuropilin-2 receptor biology as a novel target for new product candidates for a variety of diseases, including cancer and inflammatory disorders. The company's lead therapeutic candidate, ATYR1923, selectively binds to NRP2 and is currently in clinical development for inflammatory lung diseases, including a Phase 2 study in patients with COVID-19 related severe respiratory complications. "We are particularly inspired by these independent findings and they further validate ATYR1923's potential to play a role as a treatment for COVID-19. As ATYR1923 is a selective modulator of NRP2 and dampens inflammatory response, the discovery of the Neuropilin domain as a binding site to the S1 protein significantly strengthens the hypothesis that ATYR1923 may have the potential to directly modulate SARS-CoV-2 infectivity and disease pathology," said Dr. Sanjay Shukla, President and CEO of aTyr.
FB

Hot Stocks

11:09 EDT Facebook files lawsuits over unauthorized automation software - Facebook said in a statement: "Today we filed separate lawsuits in Europe and the United States to enforce our Terms of Service against the use of unauthorized automation software on Facebook and Instagram. This is one of the first times a social media company is using coordinated, multi-jurisdictional litigation to enforce its Terms and protect its users. The defendants in the European lawsuit operated a Spain-based fake engagement service, and the defendant in the US lawsuit operated a data scraping service with ties to California. These lawsuits also allege the defendants violated the laws of Spain and the US, including Spain's protections for databases and online platforms and the Computer Fraud and Abuse Act in the US. We are seeking injunctions to reinforce our permanent ban against their use of our platform. Facebook Inc. and Facebook Ireland sued MGP25 Cyberint Services and its founder in the commercial court of Madrid for providing automation software to distribute fake likes and comments on Instagram...Facebook Inc. also sued Mohammad Zaghar in federal court in San Francisco for operating a data scraping service called Massroot8." Reference Link
CUBI

Hot Stocks

11:04 EDT Customers Bank appoints Daniel Park as SVP, treasurer - Customers Bank announced Daniel Park has joined the bank as SVP and Treasurer. In his new role, Park will establish relationships with Customers Bank's business leaders to ensure Treasury is effectively delivering funding solutions to the bank's clients. He will also be responsible for continuing to enhance relationships with the bank's regulatory stakeholders as he focuses on investment portfolio management, liquidity and funding capital stress testing, as well as risk management. Most recently, Park served as Managing Director, Americas Capital Planning and Strategy at UBS.
CL

Hot Stocks

10:48 EDT Colgate evaluates Chinese toothpaste brand amid racial debates, Reuters says - Colgate-Palmolive is working on evaluating and updating Chinese toothpaste brand Darlie as companies review their brands amid racial inequality debates, Reuters' Martinne Geller reports, citing a spokesman. Darlie, which was previously named Darkie and showed a man in blackface, still has a Chinese name that translates to 'black person toothpaste'." For more than 35 years, we have been working together to evolve the brand, including substantial changes to the name, logo and packaging. We are currently working with our partner to review and further evolve all aspects of the brand, including the brand name," a Colgate spokesman said. Reference Link
KR

Hot Stocks

10:36 EDT Kroger sees Q2 EPS up in mid to high single digits
DB

Hot Stocks

10:36 EDT Deutsche Bank pays $10.25M to settle two CFTC enforcement matters - The Commodity Futures Trading Commission announced the settlement of two enforcement matters involving Deutsche Bank. In the first matter, Deutsche Bank resolved federal court charges stemming from alleged violations of various swap data reporting and other regulatory violations. In the second matter, the CFTC issued an administrative order against Deutsche Bank Securities, filing and settling charges that two of the bank's traders engaged in spoofing. According to the order, Deutsche Bank Securities manually placed bids or offers on the Chicago Mercantile Exchange with the intent to cancel those bids or offers before execution. The consent order imposes a $9M civil monetary penalty on Deutsche Bank. The administrative order requires Deutsche Bank to pay a civil monetary penalty of $1.25M.
KR

Hot Stocks

10:35 EDT Kroger expects sales to continue to taper as quarter progresses
KR

Hot Stocks

10:35 EDT Kroger: ID sales so far in Q2 trending up mid-teens - Comments taken from Q1 earnings conference call.
BIIB MYL

Hot Stocks

10:30 EDT Biogen to appeal ruling, says IBD's Allison Gatlin - IBD's Allison Gatlin said via Twitter that Biogen confirmed a District Court judge in West Virginia invalidated a key patent protecting Tecfidera. According to an emailed statement, Biogen is "disappointed" with the decision and plans to appeal the ruling. Reference Link
NVO

Hot Stocks

10:30 EDT Novo Nordisk says Phase 2 AM833 trial reached primary endpoint - Novo Nordisk announced the headline results from two clinical trials with a novel once-weekly subcutaneous amylin analogue, a Phase 2 monotherapy trial and a Phase 1 combination trial of AM833 and once-weekly subcutaneous semaglutide 2.4 mg. The 26-week blinded Phase 2 monotherapy trial with AM833 investigated safety, tolerability and efficacy for weight management in 706 people with obesity or overweight with at least one weight-related comorbidity. The patients were randomized to treatment with five different weekly doses of AM833, liraglutide 3.0 mg or placebo. Approximately 100 people were included in each treatment arm. The trial reached its primary endpoint by demonstrating a weight loss of 10.8% at week 26 with AM833 at the 4.5 mg dose, compared to a weight loss of 3.0 % with placebo, Novartis said in a statement. The treatment difference was statistically significant and AM833 appeared to have a safe and well-tolerated profile, the company added. The 20-week multiple ascending dose phase 1 trial investigated safety, tolerability, pharmacokinetics and weight loss potential of AM833 administrated in combination with semaglutide 2.4 mg in 80 people with obesity or overweight. After 20 weeks of treatment, participants receiving the highest dose lost an average of 17.1% body weight from a mean baseline body weight of 95.1 kg. The trial investigated the number of treatment-emergent adverse events and AM833 was well-tolerated, with the most common adverse events being gastrointestinal disorders including nausea and vomiting, according to Novartis.
MSFT

Hot Stocks

10:09 EDT Microsoft acquires ADRM Software, terms not disclosed - In a blog post, the company said, "We are excited to announce the acquisition of ADRM Software, a leading provider of large-scale industry data models, which are used by large companies worldwide as information blueprints. ADRM's robust industry data models have been built and refined over decades for business-critical analytics. An industry data model enables organizations to more holistically capture and define business concepts, refine and integrate processes, and build interoperability in their ecosystem. According to Gartner, "Data models are foundational for business. They undergird wide-ranging initiatives and permanent programs, such as data quality, data lineage and data governance." But companies today are implementing data modeling on a fragmented basis, resulting in a disparate data estate that is incapable of supporting the kinds of digital transformation required today. Combining comprehensive industry models from ADRM with limitless storage and compute from Azure allows for the creation of the intelligent data lake where data from multiple lines of business can be harmonized together more quickly. Together with Microsoft Azure, these capabilities will be delivered at scale, enabling our customers to accelerate digital progress, and reduce risk in a variety of major initiatives. We're excited to welcome the ADRM team to Microsoft, and together look forward to advancing the digital transformation journeys of our partners and customers."Reference Link
AMZN

Hot Stocks

10:02 EDT Amazon.com, Valentino file joint lawsuit against New York-based counterfeiter - Amazon.com and Maison Valentino Italian luxury brand announced a joint lawsuit against Buffalo, New York-based Kaitlyn Pan Group, LLC and New York resident Hao Pan for counterfeiting Valentino's Valentino Garavani Rockstud shoes, and offering the infringing products for sale, in violation of Amazon's policies and Valentino's intellectual property rights. "The vast majority of sellers in our store are honest entrepreneurs but we do not hesitate to take aggressive action to protect customers, brands, and our store from counterfeiters. Amazon and Valentino are holding this company accountable in a court of law and we appreciate Valentino's collaboration throughout this investigation," said Dharmesh Mehta, vice president, Customer Trust and Partner Support. Amazon shut down Kaitlyn Pan's seller account in September 2019. Despite multiple notices of infringement and a cease and desist order, Kaitlyn Pan continues to import, distribute, sell, and offer infringing products. Kaitlyn Pan further attempted to apply for a US trademark for its infringing Valentino Garavani Rockstud shoes, flagrantly and willfully disregarding Valentino's intellectual property.
PAR

Hot Stocks

10:00 EDT Par Technology rises 10.3% - Par Technology is up 10.3%, or $2.91 to $31.24.
ABM

Hot Stocks

10:00 EDT ABM rises 12.7% - ABM is up 12.7%, or $4.14 to $36.67.
ORN

Hot Stocks

10:00 EDT Orion Group rises 17.4% - Orion Group is up 17.4%, or 57c to $3.85.
ABM

Hot Stocks

09:47 EDT ABM rises 11.3% - ABM is up 11.3%, or $3.67 to $36.20.
RGS

Hot Stocks

09:47 EDT Regis rises 13.6% - Regis is up 13.6%, or $1.27 to $10.62.
ORN

Hot Stocks

09:47 EDT Orion Group rises 19.8% - Orion Group is up 19.8%, or 65c to $3.93.
PRSP LDOS

Hot Stocks

09:44 EDT Perspecta protest of Navy contract award denied by GAO - The bid protest made by Perspecta Enterprise Solutions (PRSP) of a Department of the Navy Space and Naval Warfare Systems Command award was denied by the Government Accountability Office, according to a post to the GAO website. Perspecta was previously unsuccessful in its defense of the "NGEN" contract with the U.S. Navy, which went to Leidos (LDOS). Reference Link
TMUS

Hot Stocks

09:39 EDT T-Mobile revises Q2 guidance, now sees postpaid net customer adds of 800K-900K - In a regulatory filing last night, T-Mobile disclosed that it now expects the following updated before tax expenses for the quarter ending June 30, 2020, which will impact net income but will be excluded from adjusted EBITDA: merger-related costs of $800M-$900M before taxes; COVID-19 costs of $350M-$450M before taxes; and non-cash Impairment related costs of $418M before taxes. "These non-cash impairment charges are preliminary, unaudited, and subject to change pending completion of our quarter-end closing review procedures," the filing said. T-Mobile also now expects postpaid net customer additions for Q2 to be between 800,000 to 900,000, primarily driven by higher postpaid other net additions. This is up from 0 to 150,000, "reflecting a faster recovery in retail than expected as well as new opportunities in T-Mobile for Business. The increase from our prior guidance is primarily driven by higher Postpaid other net additions," the filing said. Other guidance elements for Q2 remain unchanged, T-Mobile noted.
UONE

Hot Stocks

09:36 EDT Urban One trading resumes
JBLU

Hot Stocks

09:36 EDT JetBlue to operate more than half of typical capacity this summer - With the new routes and service announced today, as well as additional capacity added back into the July and August schedules, JetBlue intends to operate more than half of its typical capacity this summer to better match demand trends. Additionally, nine temporarily closed cities and several summer seasonal destinations will reopen in early July, including Chicago O'Hare International Airport and Dallas/Fort Worth International Airport.
JBLU

Hot Stocks

09:35 EDT JetBlue to reactivate some temporarily parked aircraft to support new routes
EL

Hot Stocks

09:34 EDT Estee Lauder appoints Jane Lauder as EVP, enterprise marketing and CDO - The Estee Lauder Companies announced that Jane Lauder will be named to the new role of EVP, Enterprise Marketing and Chief Data Officer, effective July 1, 2020. She will report directly to Fabrizio Freda, President and CEO, The Estee Lauder Companies. Jane will be succeeded at Clinique by Michelle Freyre, who will join the brand as SVP, General Manager, effective July 1, 2020. As ELC's first ever Enterprise Marketing and Chief Data Officer, Jane will lead the company-wide strategy to build our data-empowered, digitally-directed priorities to accelerate ELC's growth. By optimizing our vast and valuable data and integrating the company's analytic capabilities the goal is to drive breakthrough marketing and creative.
PEP

Hot Stocks

09:32 EDT PepsiCo introduces SodaStream Professional hydration platform - PepsiCo announced it is expanding the SodaStream brand into away-from-home channels with the introduction of SodaStream Professional, which it calls "an eco-friendly hydration platform." PepsiCo said: "Following a successful pilot test with key customers, the mobile-enabled platform will allow people to personalize and digitally track their water-forward beverage intake while cutting back on plastic bottles. Rolling out commercially this fall, SodaStream Professional will support the health of both consumers and the planet as businesses reimagine the future of beverage experiences."
JBLU

Hot Stocks

09:32 EDT JetBlue to add 30 new routes, launch Mint at Newark - JetBlue announced it is adding 30 new domestic routes to serve customers in markets where leisure and VFR travel is showing some signs of strength. With business travel facing a less certain recovery timeline, JetBlue says the new routes offer it the opportunity to generate revenue, bring aircraft back into service that would otherwise sit idle, and add more flying opportunities for JetBlue crewmembers. New markets will be phased in between July and October. Seats on all new routes will be available for purchase Friday, June 19. "Coronavirus has transformed airline route maps, and as we begin to see small signs of recovery, we continue to be flexible with our network plans to respond to demand trends and generate cash in support of our business," said Scott Laurence, head of revenue and planning, JetBlue. "We've selected routes where customers are showing some interest in travel again and where our low fares and award-winning experience will be noticed." JetBlue will also expand its Mint service in the broader metro area to Newark Liberty International Airport with daily nonstop service to both Los Angeles International Airport and San Francisco International Airport.
UONE

Hot Stocks

09:31 EDT Urban One trading halted, volatility trading pause
CRDNF

Hot Stocks

09:30 EDT Cardinal Resources enters into Bid Implementation Agreement with Shandong Gold - Cardinal Resources announces that it has entered into a Bid Implementation Agreement with Shandong Gold Mining, pursuant to which Shandong Gold has agreed to acquire 100% of the issued and outstanding ordinary shares in Cardinal at a price of A$0.60 cash per share, by way of an off-market takeover offer. The premium implied by the Shandong Gold Offer is a significant increase on the non-binding indicative and preliminary proposal announced by Nord Gold SE on 16 March 2020 of A$0.45775. The Shandong Gold Offer represents an attractive premium of: 75.5% to Cardinal's 20-day volume weighted average price of A$0.34 up to 13 March 20201; 39.3% to Cardinal's 20-day volume weighted average price of A$0.43 up to close of trading on 18 June 2020, being the last trading date prior to announcement of the Transaction; 29.0% to Cardinal's last closing price of A$0.465; 31.1% to Nordgold's preliminary proposal of A$0.45775 per share announced on 16 March 2020 Cardinal's Board of Directors has carefully considered the Shandong Gold Offer in consultation with the Special Committee appointed in connection with the strategic process, its financial and legal advisors. Accordingly, Cardinal's Board of Directors unanimously recommends that all Cardinal shareholders accept the Shandong Gold Offer in the absence of a superior proposal. Cardinal's Directors, who collectively hold approximately 6.37% of Cardinal's ordinary shares, intend to accept the Shandong Gold Offer in respect of all Cardinal shares they own or control by the later of 21 days after the offer is opened for acceptance and 5 days after dispatch of the Cardinal Target's Statement, in the absence of a superior proposal. Cardinal's Board of Directors has been exploring a range of potential transactions to maximise value for shareholders and considers that the Shandong Gold Offer is the best option for shareholders, in the absence of a superior proposal, and will deliver several key benefits to shareholders including: Certain and immediate value for Cardinal shareholders - ability for shareholders to realise certain and immediate value at a significant premium to Cardinal's trading price on the ASX and TSX markets. By accepting the Shandong Gold Offer, subject to the Shandong Gold Offer going unconditional, Cardinal shareholders will receive cash consideration of A$0.60 for every Cardinal share they own; No financing condition - the Shandong Gold Offer is an all-cash offer which is not subject to any financing conditions; Avoids risks associated with mine development - the Shandong Gold Offer eliminates exposure to the risks inherent in any new mine development, including financing, operational and regulatory risks. Cardinal and Shandong Gold have agreed a Bid Implementation Agreement pursuant to which the parties have given undertakings to each other to facilitate the Transaction. The Shandong Gold Offer is subject to a limited number of conditions, including: 50.1% minimum acceptance by Cardinal shareholders; Regulatory approvals, including Foreign Investment Review Board approval and approvals of certain Chinese regulatory bodies described below; No material adverse change in relation to Cardinal; and Other conditions customary for a transaction of this nature. The Bid Implementation Agreement contains customary deal protection mechanisms including "no shop", "no talk", "no due diligence", "notification" and "matching rights" restrictions. Cardinal has agreed it will not solicit any competing proposal or participate in any discussions or negotiations in relation to any competing proposal unless, in the case of discussions or negotiations, failure to do so would be a breach of the fiduciary or statutory duties of the Cardinal Directors. Under certain circumstances, an agreed break fee or reverse break fee of $3.3 million will be payable. The Shandong Gold Offer will extend to any Cardinal Shares that are issued during the offer period as a result of the exercise of Cardinal options that exist at the time of the offer opening. However, Shandong Gold has also committed to make offers to holders of certain Cardinal options to acquire those options by way of private treaty, subject to obtaining necessary regulatory approvals.
NEON

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09:29 EDT Neonode touch sensor modules selected by Easpeed to upgrade elevators - Neonode is pleased to announce that its touch sensor modules have been selected by Anhui Easpeed Technology Co. to upgrade thousands of elevators in China with holographic button panels.
JAN

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09:28 EDT JanOne launches strategic alternatives process for legacy businesses - JanOne announced the commencement of a strategic alternative process for its legacy businesses in an effort to enhance shareholder value. This review process will be conducted with the assistance of the company's financial and legal advisors and will consider the full range of potential strategic alternatives with respect to its legacy businesses. This will include but is not limited to, acquisitions, business combinations, joint ventures, spin-offs, public and private capital raises, recapitalization, and sale transaction options. There can be no assurances that the exploration of strategic alternatives will result in any transaction. The company does not intend to discuss or disclose developments with respect to the process until it is determined that further disclosure is appropriate or required by regulation or law. No formalized timetable has been established for the completion of the strategic review.
AEMD

Hot Stocks

09:21 EDT Aethlon Medical announces FDA approval of IDE supplement for COVID-19 patients - Aethlon Medical announced that the U.S. FDA has approved a supplement to the company's existing Investigational Device Exemption for the company's Hemopurifier in viral disease to allow for the testing of the Hemopurifier in patients with SARS-CoV-2/COVID-19 in a new feasibility study. The feasibility study, which is the device equivalent of a phase 1 trial, will enroll up to 40 subjects at up to 20 centers in the U.S. Subjects will have established laboratory diagnosis of COVID-19, be admitted to an intensive care unit and will have acute lung injury and/or severe or life threatening disease among other criteria.
CWK

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09:21 EDT Cushman & Wakefield, Matterport enter into global agreement - Matterport announced a global agreement with Cushman & Wakefield. Matterport said in a release, "With Matterport Capture Services, Cushman & Wakefield will be able to offer clients a turnkey solution to scan commercial properties in 3D across its footprint."
INGIY

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09:20 EDT Ingenico reaches $1B in transactions in 18 months of Russian Payments Solutions - Ingenico Group reveals that within 18 months of going live, its Russian Payments Solution has outperformed all expectations with impressive payment volumes and customer adoption. It is now one of the fastest growing payments offerings from Ingenico ePayments, providing unique local acquiring and payment capabilities for international businesses selling online to Russian consumers in digital goods, retail, travel and more.The success of the solution is credited to Ingenico's deep understanding of the Russian financial system and partnerships it has built within the Russian banking ecosystem. Through these partnerships Ingenico developed a unique solution with local access to the Russian financial system and payment landscape providing local acquiring, local payment methods and multi-currency processing capabilities. Ingenico has rapidly grown its new solution - up to a billion in USD flow in its first 18 months - and is seeing impressively high payment approval rates. By working with leading acquiring banks such as Sberbank and Alfa Bank, Ingenico has seen impressive approval rate increases of up to 20% for customers. A high approval rate is crucial for online businesses as it leads to more online sales, lower shopping cart abandonment and returning customers.
PFE SGMO

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09:20 EDT Pfizer, Sangamo announce updated follow-on data from Alta study - Pfizer (PFE) and Sangamo (SGMO) announced updated follow-up data from the Phase 1/2 Alta study of giroctocogene fitelparvovec, an investigational gene therapy for patients with severe hemophilia A. All five patients with severe hemophilia A who received the 3e13 vg/kg dose showed sustained factor VIII, or FVIII, activity levels, with a median of 64.2% via chromogenic assay. No patients experienced bleeding events or required FVIII infusions. The factor VIII activity levels reflect measurements up to 61 weeks, the extent of follow-up for the longest-treated patient in the cohort. These data are being presented today as a late-breaking oral abstract at the World Federation of Hemophilia world congress. Giroctocogene fitelparvovec was generally well tolerated. As previously reported, one patient in the 3e13 vg/kg dose cohort had a treatment-related serious adverse event of hypotension and fever, with symptoms of headache and tachycardia, which occurred six hours post-infusion with giroctocogene fitelparvovec, and which fully resolved within 24 hours. No other treatment-related serious adverse events were reported. Among the five patients in the 3e13 vg/kg dose cohort, four received corticosteroids for liver enzyme elevations. Three patients had subsequent ALT elevations that responded to corticosteroids. All episodes of ALT elevations fully resolved with oral corticosteroids.
TFFP

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09:17 EDT TFF receives orphan drug designation for Tacrolimus Inhalation Powder - TFF Pharmaceuticals announced that the FDA has granted orphan drug designation to Tacrolimus Inhalation Powder for prophylaxis of lung allograft rejection. TFF said in a release, "Tacrolimus Inhalation Powder is an inhaled dry powder version of tacrolimus, an immunosuppressive drug used in solid organ transplants.Prograf is currently the second most commonly administered immunosuppressive agent in solid organ transplantation despite what the Company believes to be the many challenges for patients and physicians when used for extended periods. Prograf, when delivered orally or intravenously, has been shown to have numerous serious side effects including nephrotoxicity, particularly when used in high doses. The Company intends tobegin Single Ascending Dose Phase I studies in Tacrolimus Inhalation Powder later this month in Australia, withMultiple Ascending Dose studies beginningin Q3-2020."
FCBP

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09:15 EDT First Choice Bank promotes Lorraine Lee to EVP, CSO, head of commercial banking - First Choice Bancorp announced the promotion of Lorraine Lee to EVP, chief strategy officer & head of commercial banking, reporting to President & CEO Robert Franko. Ms. Lee previously served as SVP, CSO, a position she held at the Company since January 2018. Ms. Lee began her career at First Choice Bank in 2014 as First Vice President/Relationship Manager in the Commercial Lending Division.
TSCO

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09:15 EDT Tractor Supply appoints Melissa Kersey Chief Human Resources Officer - Tractor Supply announced that Melissa Kersey has been named Executive Vice President, Chief Human Resources Officer, effective July 20. Kersey, who brings senior-level experience from Walmart and, most recently, McDonald's USA, will report to Hal Lawton, Tractor Supply's President and CEO, and will serve on the Company's Executive Committee. Melissa Kersey most recently served as the Senior Vice President and Chief People Officer for McDonald's USA.
BIIB MYL

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09:14 EDT Biogen falls after judge says Mylan proved Tecfidera patent invalid - A judge in the U.S. District Court for the Northern District of West Virginia has ruled that Mylan (MYL) has "demonstrated by clear and convincing evidence that the asserted claims" of Biogen's (BIIB) U.S. Patent No. 8,399,514 are "invalid for lack of written description," according to a ruling posted to the court's website. The '514 patent is associated with Tecfidera, Biogen's product approved by the FDA for use in the treatment of multiple sclerosis. Mylan has filed an Abbreviated New Drug Application, or "ANDA," seeking to market a drug that is bioequivalent to Tecfidera. In morning trading following the patent ruling, Biogen shares are down $20.96, or 7.5%, to $260.50, while Mylan shares are up 53c, or 3.3%, to $16.50.
EXPI

Hot Stocks

09:14 EDT eXp World Holdings appoints Courtney Chakarun as CMO - eXp World Holdings announced the appointment of Courtney Chakarun to the role of chief marketing officer. She will be responsible for amplifying the eXp World Holdings' brands and overseeing all areas of marketing, including driving digital strategy for growth and enhancing eXp Realty's value proposition for agents and brokers. In addition, Chakarun will help raise awareness of VirBELA's virtual platform as more companies search for technologies and tools to solve for remote workforces. Chakarun recently was CMO of Roostify, a digital lending platform that processes nearly $35 billion a month in home loans.
ADMP

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09:13 EDT Adamis Pharmaceuticals announces publication on higher doses of naloxone - Adamis Pharmaceuticals announced the publication of an article entitled "Higher naloxone dosing in a quantitative systems pharmacology model that predicts naloxone-fentanyl competition at the opioid mu receptor level" in the peer reviewed publication "PLOS ONE, " This study was done in collaboration with Rosa and Co. Naloxone is an opioid antagonist used to treat narcotic overdoses. Naloxone works by reversing the detrimental effects of the opioid, including slowed breathing, brain dysfunction, loss of consciousness and death. Common opioids include morphine, heroin, tramadol, oxycodone, hydrocodone and fentanyl. Rapid resuscitation of an opioid overdose with naloxone, an opioid antagonist, is critical as opioid induced toxicity results in rapid death, i.e., delaying adequate resuscitation can result in death. Accordingly, the current approved naloxone doses, since they both give similar systemic exposure levels, might very well not be sufficient to reverse high doses of fentanyl. Fentanyl, a synthetic opioid, is considered 50 to 100 times more potent than morphine. According to the CDC, powerful synthetic opioids, like fentanyl and its analogues, are responsible for the largest number of deaths from opioid overdoses. To this end, it was recently reported that drug overdoses in British Columbia last month killed more people there than COVID-19 has all year. The vast majority of the overdose deaths involved fentanyl. There is no reason to believe that this same trend is not happening in the U.S. The manuscript describes an opioid receptor quantitative systems pharmacology model which was developed to predict the effects of different IM doses of naloxone in response to different levels of fentanyl exposure. The model defined a successful reversal as lowering the amount of opioid bound to the brain receptors to less than 50% within 10 minutes. For the lowest and middle levels of fentanyl exposure, the model predicted that the 2 mg IM naloxone resulted in successful resuscitations within ten minutes, but more rapid reversal was observed with the 5 and 10 mg doses. However, at the highest level of naloxone exposure, the model predicted that the 2 mg IM doses of naloxone did not result in a successful reversal. In contrast, the 5 and 10 mg doses of naloxone successfully reversed opioid toxicity.
TSN

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09:11 EDT Tyson Foods appoints Dan Turton as SVP, global government affairs - Tyson Foods named Dan Turton as SVP, Global Government Affairs, effective June 29, 2020. Turton will be based in Washington, D.C. and will lead the worldwide government relations activities for the Company. He will report to Amy Tu, EVP and General Counsel. Most recently, Turton served as a Senior Advisor to the U.S. House of Representatives Committee on Rules.
INTC SGH

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09:10 EDT Penguin Computing joins Intel Select Solutions program - Penguin Computing (SGH) announced an expansion of its partnership with Intel Corporation (INTC) and is now participating in the Intel Select Solutions program. Penguin Computing will deliver a series of verified quick-to-deploy infrastructure solutions optimized for HPC and AI/ML applications. Penguin Computing's goal through this collaboration is to empower customers to leverage the power of HPC and AI through reference designs. These reference designs are optimized for a range of broadly used HPC and AI/ML applications thereby lowering the technical barriers and accelerating the customer's market competitiveness. As organizations strive to stay ahead of the rapidly changing technological demands for HPC and AI infrastructures, they increasingly turn to partnerships that can help them navigate those complexities and deliver value to their customers. Intel Select Solutions simplify and accelerate the deployment of workload-optimized infrastructure through a suite of solution configurations that have been rigorously benchmark-tested and are optimized for real-world performance. Every Intel Select Solution is built to meet the highest thresholds of resiliency, system agility and service reliability. In concert with Intel, Penguin Computing will develop and deliver multiple Intel Select Solutions focused on the transformational promise of HPC and AI/ML in the enterprise through collaboratively designed simplicity.
BRQS

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09:09 EDT Borqs signs term-sheet for strategic alliance with China Health Industries - Borqs Technologies announced that the Company has signed a non-binding term-sheet on June 16, 2020 with China Health Industries Holdings, where CHHE intends to purchase up to $12 million of BRQS ordinary shares at the market price and warrants which have a two-year term and are exercisable at a premium of 25% above the sales price of the ordinary shares. BRQS intends to use the proceeds of the CHHE investment for working capital and to form a new joint-venture subsidiary with CHHE particularly for the development and the procurement of mobile connected medical IoT products based on Qualcomm's 5G technology. China Health Industries Holdings, Inc., through its wholly owned subsidiary, Harbin Huimeijia Biotechnology, engages in R&D, manufacturing and distribution of medical devices, drugs and health products in China licensed by the China Food and Drug Administration. HHMJ Biotech is also registered with the U.S. Food and Drug Administration as a manufacturer of surgical apparel accessories, protective clothing and shields, particularly contributing to the containment of the current COVID-19 pandemic. Both Borqs and CHHE are envisioning huge and new markets for connected medical IoT products and applications based upon the ultra-high speed 5G mobile technology. The transaction is subject to the signing of definitive documents within the next several weeks.
NUE

Hot Stocks

09:08 EDT Nucor says Q2 operating performance 'better than expected' - The company said, "Nucor's better-than-expected second quarter performance reflects both the power of our culture and the strength of our business model. By working hard and working together, the 27,000 men and women on the Nucor Team have done an excellent job of taking care of each other, our customers, and our shareholders. Second quarter operating performance has been better than expected and we have estimated our guidance range accordingly. Though overall market conditions are still challenged by the pandemic, demand in nonresidential construction has been resilient during this time. Nucor's downstream steel products segment is having another strong quarter. In our steel mills segment, the impacts of the COVID-19 pandemic have most negatively impacted our sheet and plate mills due to weak oil and gas market activity and customer production disruptions. Although domestic automotive production was halted due to COVID-19 concerns, we are seeing a strong rebound in automotive related steel demand. The automotive industry experienced better than expected sales during their outage period resulting in low inventory levels as we enter the third quarter of 2020. Our raw materials segment has been challenged by decreased pricing for raw materials and the impact of an outage at our DRI facility in Trinidad to comply with that country's stay at home orders. We believe Nucor is well positioned to navigate any future challenges that arise from these current situations given our advantaged cost position, flexible production capability and financial strength. We were pleased to be able to further enhance our financial flexibility with the recent issuance of $500.0 million of 2.000% notes due 2025 and $500.0 million of 2.700% notes due 2030."
NTRA

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09:07 EDT Natera enrolls first patients in two tests using Signatera MRD Testing - Natera has begun enrollment in the CIRCULATE-Japan and BESPOKE CRC trials. The studies will measure clinical outcomes of Signatera molecular residual disease - or MRD - testing in resectable Stages II-IV colorectal cancer. The CIRCULATE-Japan trial, organized by the National Cancer Center Japan, is a prospective, multi-center, randomized trial that will investigate optimal circulating tumor DNA-guided treatment strategies for patients with resectable Stage II-IV CRC, particularly adjuvant chemotherapy decisions based on MRD status. The study will include 2,500 patients from approximately 150 cancer centers across Japan. Natera also recently enrolled the first patient in its BESPOKE CRC study, another prospective, multi-center trial that will enroll 1,000 or more patients at time of surgery to measure the clinical impact of serial blood-based testing with Signatera, earlier relapse detection, and better patient risk stratification after surgery.
FTNT

Hot Stocks

09:07 EDT Fortinet achieves MEF 3.0 SD-WAN certification - Fortinet announced that Fortinet Secure SD-WAN has been certified to support MEF 3.0 SD-WAN services. This certification aims to establish a common language for defining SD-WAN technologies and enables communication service and technology providers to validate that their solutions comply with the highest industry standards for performance, assurance, and agility.
NXPI...

Hot Stocks

09:07 EDT NXP, MasterCard, Xiaomi expand reach for mobile payments into Europe - NXP Semiconductors (NXPI), Mastercard (MA), and Xiaomi (XIACF) announced they are bringing more convenient and secure contactless experiences to Russia as the first phase of a European-wide roll-out with NXP's mobile wallet solution. Powering mobile payments for Xiaomi's Mi Smart Band 4 NFC wearable devices, NXP's mWallet 2GO supports an accelerated roll-out across Europe by addressing OEMs' needs for easy, yet secure and scalable, wallet implementations. It also addresses user demands to quickly enable payment devices by digitizing their bank cards and experience smooth NFC transactions at the Point-of-Sale. The collaboration builds on the companies' successful history in driving tap-to-ride mobile transit experiences in Beijing, Guangxi, Shenzhen and other several major Chinese cities with some of the world's busiest metro stations and public bus lines. The Xiaomi Mi Band 4 offers the industry's best price-to-performance ratio for fully-active, NFC- and SE-based and EMVCo-certified payment devices.
EVOL

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09:04 EDT Evolving Systems reports 15-year anniversary of partnership with Asian operator - Evolving Systems announced two milestone achievements. First, the partnership between the two companies has now passed the fifteen year mark, an unusually long relationship in the rapidly changing telecommunications industry; and second, the operator's subscriber base has reached 45 million customers. Evolving Systems has worked with the operator since its inception. Presently, the two are embarking on a new project to implement changes that will allow the operator's customers to enjoy full 4G services as the company rolls out its Voice over LTE offering.
PHG

Hot Stocks

09:03 EDT Philips announces collaboration with American Telemedicine Association - Royal Philips announced it has once again joined forces with the American Telemedicine Association to help further the adoption of telehealth across the industry, demonstrating its commitment to connecting care across acute, post-acute and home care settings. The continued collaboration spotlights the growing adoption and momentum in telehealth amidst COVID-19, and the need to convey the exponential shift to telehealth capabilities. In response to the pandemic, Philips has been working with customers around the world to rapidly develop and deploy scalable telehealth solutions to support frontline care professionals and their patients. Philips recently received 510(k) clearance from the Food and Drug Administration for its wireless wearable biosensor to help manage confirmed and suspected COVID-19 patients in the hospital. The wearable biosensor enhances clinical surveillance as part of the Philips patient deterioration detection solution to help clinicians detect risk so they can intervene earlier and help improve care for patients in lower acuity care areas.
NUE

Hot Stocks

09:03 EDT Nucor says Q2 operating performance 'been better than expected' - The company said, "Nucor's better-than-expected second quarter performance reflects both the power of our culture and the strength of our business model. By working hard and working together, the 27,000 men and women on the Nucor Team have done an excellent job of taking care of each other, our customers, and our shareholders. Second quarter operating performance has been better than expected and we have estimated our guidance range accordingly. Though overall market conditions are still challenged by the pandemic, demand in nonresidential construction has been resilient during this time. Nucor's downstream steel products segment is having another strong quarter. In our steel mills segment, the impacts of the COVID-19 pandemic have most negatively impacted our sheet and plate mills due to weak oil and gas market activity and customer production disruptions. Although domestic automotive production was halted due to COVID-19 concerns, we are seeing a strong rebound in automotive related steel demand. The automotive industry experienced better than expected sales during their outage period resulting in low inventory levels as we enter the third quarter of 2020. Our raw materials segment has been challenged by decreased pricing for raw materials and the impact of an outage at our DRI facility in Trinidad to comply with that country's stay at home orders. We believe Nucor is well positioned to navigate any future challenges that arise from these current situations given our advantaged cost position, flexible production capability and financial strength. We were pleased to be able to further enhance our financial flexibility with the recent issuance of $500.0 million of 2.000% notes due 2025 and $500.0 million of 2.700% notes due 2030."
NOK T

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09:02 EDT Nokia, AT&T run trial of RAN Intelligent Controller over commercial 5G - Nokia (NOK) and AT&T (T) announced a successful limited live trial of the RAN Intelligent Controller over AT&T's commercial 5G mmWave network in New York City. Once fully implemented into the network, the RIC platform will enable increased network optimization capabilities through policy-guided, closed loop automation. Last year, AT&T and Nokia announced their collaboration to co-develop the RIC software platform, in alignment with the O-RAN Alliance target architecture, to accelerate the creation of open source software for the 5G RAN. The intent is to create open interfaces and an open ecosystem of interoperable components that will enable rapid, flexible service deployments and programmability within the RAN. The RIC software is available at the O-RAN Software Community. For the recent trial, AT&T and Nokia ran a series of external applications, called "xApps," at the edge of AT&T's live 5G mmWave network on an Akraino-based Open Cloud Platform. The xApps used in the trial were designed to improve spectrum efficiency, as well as offer geographical and use case-based customization and rapid feature onboarding. Ultimately, the trial achieved its test goals. Both companies tested the RAN E2 interface and xApp management and control, collected live network data using the Measurement Campaign xApp, the neighbor relation management using Automated Neighbor Relation xApp, and tested RAN control via the Admission Control xApp - all with zero interruption to the live commercial network.
DBI

Hot Stocks

09:01 EDT Designer Brands sees continuing promotional activity, may pressure margins
DBI

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09:01 EDT Designer Brands will continue to refrain from providing guidance
CNDT

Hot Stocks

08:59 EDT Conduent announces implementation of ticketing system for Brescia Mobilita - Conduent Transportation announced the implementation of a new account-based ticketing system for Brescia Mobilita's light metro transit network in northern Italy. Each day, approximately 50,000 people use the Brescia Metro system. The company launched the new system allowing riders to access the service using major contactless credit and debit cards, including Mastercard, Visa, American Express, VPay, Visa Electron and Maestro. NFC-enabled devices, such as smartphones and smart watches with digital wallets, such as Apple Pay, Samsung Pay, and Google Pay, can also be used.
CATM

Hot Stocks

08:58 EDT Cardtronics collaborates with Pin4 to launch mobile cash service in UK - Cardtronics announced its ATMs would be the first in the U.K. to allow individuals to withdraw cash using a new cardless cash service from fintech solutions provider Pin4. The Pin4Cash service will enable organizations to send cash to individuals in real-time using an SMS text message. This unique and innovative solution allows people to complete card-free cash withdrawals at the majority of Cardtronics' CashZone ATMs around the country using only their mobile device, without requiring a payment card.Businesses, charities, and government agencies can now use Pin4Cash to send people in the U.K. a simple text message containing a unique code the individual can use to access the funds at a participating Cardtronics ATM location. Once at the ATM, the individual enters their phone number, the unique code, and their four-digit pin, with no card required. The Pin4Cash solution offers a simple, easy way for organizations to pay wages, issue hardship funds, and provide cash incentives and awards, even to those without banking accounts or debit cards.
KMPH

Hot Stocks

08:57 EDT KemPharm extends cash runway past March 2, 2021 PDUFA date - The company said, "As I noted above, Q1 2020 was our third consecutive quarter of development services revenue. We expect this trend to continue through the remainder through 2021 as we continue to work with our partners to advance the development of our various product candidates and, if approved, to support the commercial launch of KP415 potentially during the second half of 2020. The combination of continuing services revenue, an improved expense base, completing the first phase of restructuring of our 2020 debt obligations, and the $5 million regulatory milestone earned under the KP415/KP484 License Agreement as a result of the FDA's acceptance of the KP415 NDA, has extended our cash runway past the potential March 2, 2021 PDUFA date for the KP415 NDA and up to the debt maturity date of March 31, 2020. Beginning in early 2019, we have undertaken measures to improve our financial position, including a 36% reduction in our workforce, as well as other G&A cost reductions, shifting development costs to our partners, and adding development services revenue. We are continuing to work with our financial advisors to complete the second phase of debt restructuring, which we will seek to complete, if possible, prior to the potential approval of the KP415 NDA. While challenging, we remain optimistic that a solution is possible. As a fellow shareholder and the first investor, I remain focused on addressing this issue in the most favorable manner possible to us. Regarding our listing status with Nasdaq, on May 19, 2020, KemPharm received a letter from the Nasdaq Hearings Panel notifying us that since it was unable to regain compliance with the $35 million minimum market value of listed securities requirement by May 13, 2020, the Hearings Panel had elected to delist the Company's shares from trading on Nasdaq. In response, we submitted, and OTC Markets accepted, KemPharm's application for trading of its common shares on the OTC Markets Venture Market, where our shares have continued trading under the same ticker symbol, "KMPH." Throughout the Nasdaq appeals process, KemPharm explored many options, including highly dilutive financings and reverse stock splits that could potentially assist in maintaining our listing on Nasdaq. However, after careful evaluation, we determined that the measures necessary to fulfill the Nasdaq listing requirements would not serve the longer-term interests of the Company or its shareholders. Our hope is that the multiple, near-term growth opportunities related to KP415 and our development pipeline could provide momentum for KemPharm to potentially return to trading on Nasdaq, or potentially other alternatives that become available."
KMPH

Hot Stocks

08:53 EDT KemPharm working with Corium to determine steps for development pipeline - The company said, "Now that the KP415 NDA is under FDA review, we have begun working with the team at Corium to determine the next steps in advancing our other product candidates, which includes KP484, KP879 and KP922. After KP415, KP484 is our next most advanced product. In many ways, the clinical development program for KP484 is expected to mirror the KP415 program. However, we expect to gain important time and cost efficiencies since KP484 is also based on our prodrug, SDX. For example, we plan to reference certain pharmacokinetic data, as well as the results of the human abuse potential trials from the KP415 program in a potential future NDA for KP484. The advancement of KP879 and KP922, as well as KP484, will depend on input from GPC and Corium. KP879 is ready for us to submit an Investigational New Drug application with the FDA, and, if given the go-ahead, we could submit that IND later this year. Similar to both KP415 and KP484, each of our other pipeline product candidates has the potential to fulfill key unmet needs in their respective target patient populations. In fact, KP879 is the first product candidate to be designed and developed to treat stimulant use disorder. As such, it may qualify for Fast-Track status with the FDA, as well as potentially be designated as a Breakthrough Therapy and/or Orphan Drug. These designations could potentially enable a priority review process with the FDA and possibly lead to other development and cost-saving advantages. In addition to KemPharm's current product development pipeline, we are working with Deerfield to identify up to two additional compounds where KemPharm's Ligand Activated Therapy technology could be applied to develop new prodrug candidates that address unmet needs. Deerfield has a history of supporting the development and commercialization of innovative drug therapies and is uniquely positioned with its network of portfolio companies to identify and evaluate the commercial potential of various product candidates across a broad spectrum of therapeutic areas. We believe that the debt restructuring activities that occurred in December 2019, combined with their interest in future investment in prodrug discovery, demonstrates that Deerfield remains a solid financial partner that continues to value the long-term potential of KemPharm's team, technology and future product opportunities. With regard to APADAZ, KemPharm continues to work closely with our licensing partner, KVK-Tech, Inc. Despite the challenging environment for prescription opioids, KVK has made important progress in several areas. Specifically, KVK made APADAZ available nationally through its distributor network for pharmacies to stock beginning in November 2019, 23 states have added the authorized generic form of APADAZ to their Medicaid preferred drug lists, and just recently, APADAZ and its authorized generic was added to the Federal Supply Schedule. We are encouraged by this progress and hope to continue providing material updates as we received them from KVK."
ALL

Hot Stocks

08:52 EDT Allstate reports May estimated catastrophe losses of $350M - Allstate announced estimated catastrophe losses for the month of May of $350 million, pre-tax ($277 million, after-tax). Allstate said in a release, "Catastrophe losses occurring in May comprised eight events at an estimated cost of $346 million, pre-tax ($273 million, after-tax), plus unfavorable prior period reserve reestimates. Four severe weather events which included rain, wind and hail, primarily impacting Texas and the Midwest, accounted for approximately 80% of May estimated catastrophe losses. Allstate previously announced $632 million, pre-tax ($499 million, after-tax), in estimated catastrophe losses for the month of April 2020, bringing estimated catastrophe losses for the months of April and May 2020 to $982 million, pre-tax ($776 million, after-tax)."
KMPH

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08:52 EDT KemPharm updates outlook on GPC, Corium agreement - The company said, "As I mentioned previously, KemPharm entered into the KP415/KP484 License Agreement in September 2019, which provided GPC and its affiliates exclusive worldwide rights to develop, manufacture and, if approved, commercialize product candidates containing SDX and d-MPH, including KP415 and KP484. The terms of the deal entitle KemPharm to earn up to $493M in milestone payments, which includes a $10 million upfront payment, a $5 million regulatory milestone payment upon the FDA's acceptance of the KP415 NDA, approval milestone payments related to KP415 and KP484 of up to $58 million, and royalties on U.S. net sales of up to 25%, and royalties on ex-U.S. net sales of up to 9%. In addition, GPC will provide reimbursements of up to $8 million in third-party product development costs for KP415 and all future development costs for KP484. Further, the KP415/KP484 License Agreement provides GPC the option to license two additional prodrug candidates from KemPharm: KP879 for the treatment of Stimulant Use Disorder, and KP922, our prodrug of amphetamine for the treatment of ADHD. In addition, KemPharm earns research and development services revenue under the KP415/KP484 License Agreement, and Q1 2020 marked KemPharm's third sequential quarter of reporting such revenue. We expect to continue generating revenue into the foreseeable future as we support the potential launch of KP415 and the potential development of KP484. Under the KP415/KP484 License Agreement, our next milestone payment will be earned if the KP415 is approved on its PDUFA date of March 2, 2021. The amount of the milestone payment will be based on KP415's final approved label. With all of the economic opportunity available to KemPharm under the KP415/KP484 License Agreement, the true value of KemPharm's relationship with GPC cannot be measured entirely in dollars and cents. GPC and Corium are motivated by a strong belief in the potential of KP415 and KemPharm's other product candidates to transform the ADHD treatment landscape. This enthusiasm was clearly evident as we worked closely with the GPC team during all phases of preparing the KP415 NDA for submission to the FDA. Our collaboration led to what we believe is a strong NDA package for KP415. This outlook was affirmed by the FDA in the Day-74 letter, which stated that the KP415 NDA is "...sufficiently complete to permit a substantive review..." Both KemPharm and the GPC team were very pleased that there were no unexpected questions or requests for clarifications in the letter. In Corium, KemPharm has aligned with what we believe is the best organization to lead the potential commercialization of KP415. Mr. Sternberg and his team have successfully commercialized numerous products targeting large patient populations, and their expertise in the ADHD space is unmatched. Success in anything is never a certainty, but the more experience, knowledge and passion one possesses, the greater the likelihood of achieving one's goals. Working with Corium, and backed by GPC, we believe that KP415 is in prime position to capture a sizeable portion of the ADHD market and bring meaningful benefits to physicians, patients and their families. We look forward to working together with our partners at GPC and Corium to support the ongoing regulatory process and commercial preparation activities needed to facilitate a potential launch of KP415 in the second half of 2021, if approved."
WRTC

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08:51 EDT Wrap Technologies announces new international purchase orders - Wrap Technologies announced the company has received new international purchase orders from three countries in Asia for over 200 BolaWrap devices, more than 2,600 cartridges and accessories. The company said in a release, "Two purchase orders are follow-on orders from demonstrations and trainings conducted last year. The third purchase order is an initial order from a new country beginning BolaWrap demonstrations and trials this year. Wrap expects to recognize the revenue on these orders in Q2 of 2020."
WCAGY

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08:51 EDT Wirecard auditor can't find evidence of missing EUR 1.9B in cash - Wirecard said its auditor Ernst & Young GmbH Wirtschaftsprufungsgesellschaft informed the company that no sufficient audit evidence could be obtained so far of cash balances on trust accounts to be consolidated in the consolidated financial statements in the amount of EUR 1.9B. It stated, "There are indications that spurious balance confirmations had been provided from the side of the trustee respectively of the trustee's account holding banks to the auditor in order to deceive the auditor and create a wrong perception of the existence of such cash balances or the holding of the accounts for to the benefit of Wirecard group companies. The Wirecard management board is working intensively together with the auditor towards a clarification of the situation. In light of the above the audit of the annual and the consolidated financial statements 2019 will not be concluded as planned by June 18, 2020. A new date will be announced. If certified annual and consolidated financial statements cannot be made available until June 19, 2020, loans made to Wirecard AG amounting to approximately EUR 2 billion can be terminated."
KMPH

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08:50 EDT KemPharm collaborating Corium to support KP415 NDA review process - The company said, "The ADHD market accounts for approximately $17.9 billion of revenue in 2019 with a year-over-year prescription growth rate greater than four percent. Within this, the branded portion of the ADHD market was approximately $7.4 billion in 2019, with extended release products representing more than 97% of the branded prescriptions. In 2019, the methylphenidate portion of the ADHD market accounted for approximately 20 million prescriptions and $4.9 billion in sales. Over the last several years, Jornay PM is the only new MPH product that has been introduced to the market. However, our research suggests that prescribers and patients remain eager for truly innovative new treatment options. KP415 is based on serdexmethylphenidate, which is KemPharm's prodrug of d-methylphenidate, which, if approved, would be the first prodrug of methylphenidate made available to the ADHD market. KemPharm designed both KP415 and KP484 to specifically target several key unmet needs with the most widely prescribed MPH treatments for ADHD. With respect to KP415, its target design attributes include improving onset of action, providing consistent therapy with a longer duration, and reducing abuse potential. Based on the data obtained from KP415's clinical program, we believe these design goals have been met. Now, we are collaborating with Corium to support the NDA review process which will determine the final label for KP415, and, if approved, to bring these potential benefits to the ADHD market. While KP415 is designed to be used across several age groups and with a variety of patient types, KP484 is more specifically aimed at post-adolescent patients who require a full-day treatment option for their ADHD symptoms. KP484 is included in the KP415/KP484 License Agreement, and the team at Corium is actively evaluating the potential value and timing of the product development plan. We will share material updates with you as we receive them. I am also pleased to inform you that several additional patents for SDX were issued over the past few months which we expect will allow continued intellectual property protection for SDX and any product containing SDX, until at least the year 2037. The potential to have a 16-year product life from PDUFA is a truly unique opportunity arising from the underlying prodrug IP and is exciting when considering the lifetime commercial potential of KP415. For those who closely follow the ADHD space, products with the expected attributes of KP415 and KP484 are highly desirable given the lack of innovation in the market over the last 15 years. Not since Vyvanse was approved in 2007 has there been a product brought to market with significantly new properties or benefits. It is this vast potential, as well as the collective abilities and experience of KemPharm's development team, that enabled us to secure the KP415/KP484 License Agreement, and through that, have the opportunity for the Corium team, led by Mr. Sternberg, to spearhead the commercialization of KP415."
ABBV

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08:49 EDT AbbVie's Rinvoq meets efficacy endpoints in Phase 3 dermatitis study - AbbVie announced upadacitinib monotherapy met the co-primary endpoints of at least a 75% improvement in the Eczema Area Severity Index and a validated Investigator's Global Assessment for Atopic Dermatitis of clear or almost clear at week 16 in adults and adolescents with moderate to severe atopic dermatitis who are candidates for systemic therapy. Measure Up 1 is the first pivotal Phase 3 study to evaluate the efficacy and safety of RINVOQ for the treatment of moderate to severe atopic dermatitis. In this study, patients receiving either 15 mg or 30 mg of upadacitinib monotherapy showed significant improvement in skin clearance. Of patients receiving upadacitinib 15/30 mg, 70/80% achieved EASI 75 at week 16, respectively, versus 16% in the placebo group. Of those treated with upadacitinib 15/30 mg, 48/62% of patients achieved vIGA-AD 0/1, respectively, versus 8% of patients receiving placebo. For both doses, patients experienced an early reduction in itch, which was maintained through week. Atopic dermatitis is a common, chronic, relapsing, inflammatory skin disease that can manifest as a recurring cycle of itching and scratching leading to painful, cracked skin, affecting up to an estimated 25% of adolescents and 10% of adults at some point in their lifetime.No new safety risks were observed compared to the safety profile observed in patients with rheumatoid arthritis and psoriatic arthritis receiving RINVOQ. Full results from Measure Up 1 will be presented at a future medical meeting and published in a peer-reviewed publication.
KMPH

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08:48 EDT KemPharm 'optimistic' about short-, long-term prospects - KemPharm announced that Travis Mickle, Ph.D., President and CEO of KemPharm, has issued a Letter to Shareholders in connection with the Company's 2020 Annual Meeting of Stockholders to be held on June 19, 2020. The letter provides an update on recent events and outlook for the remainder of 2020 and early 2021. "The last twelve months have been a period of significant advancement for KemPharm. While challenges certainly remain, there are also significant reasons for optimism. Just recently, the New Drug Application for KP415, our investigational product candidate for the treatment of attention deficit hyperactivity disorder, was successfully filed and accepted by the U.S. Food and Drug Administration. In addition, we recently received Day-74 Letter from the FDA which set the action date for KP415 as March 2, 2021. I am also pleased to pass along that there were no information requests included in the letter from the FDA that were not already expected, and the FDA informed us that an advisory committee is not required at this time. The FDA's acceptance of the KP415 NDA has triggered two important developments in our collaboration with Gurnet Point Capital and its affiliates. First, KemPharm earned and has since received the $5 million milestone payment as provided by the definitive collaboration and license agreement we entered into with an affiliate of GPC on September 3, 2019. Second, we were pleased to announce Corium, a GPC portfolio company, will lead all commercialization activities for KP415. Corium is led by several executives with significant experience in the commercialization of ADHD products, including its President and Chief Executive Officer, Perry Sternberg. Mr. Sternberg previously served a dual role at Shire as the Head of U.S. Commercial for seven therapeutic area business units, as well as the Chief Commercial Officer/Head of the Neuroscience Division, prior to the acquisition of Shire by Takeda Pharmaceutical Corporation Limited. During his tenure at Shire, Mr. Sternberg was responsible for bringing forth several groundbreaking ADHD products, including Vyvanse. Working with our existing debtholders, led by Deerfield Management, we were also able to complete an initial restructuring of our outstanding debt in December 2019, which allowed us to extend all principal and interest payments to a new maturity date of March 31, 2021, which is past the PDUFA date for KP415. This has extended our cash runway and allows us to capitalize on the opportunities that arise from the KP415/KP484 License Agreement and the potential approval of KP415 to negotiate a long-term restructure of our balance sheet. Based on these recent events and accomplishments, we are very optimistic about KemPharm's short- and long-term prospects. This enthusiasm is rooted in three core beliefs: KP415, if approved, has the potential to reshape the ADHD treatment landscape, particularly the methylphenidate product market; Corium possesses the most well-suited and experienced commercial organization to launch and maximize the potential market for KP415; and Addressing KemPharm's debt is an achievable goal."
GNUS BABA

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08:45 EDT Genius Brands says John Landis joins 'Stan Lee's Superhero Kindergarten' team - Genius Brands International (GNUS) announced that John Landis will join Arnold Schwarzenegger and the production team behind Genius Brands' new children's animated series, Stan Lee's Superhero Kindergarten. Landis will direct Schwarzenegger, who lends his voice to the starring role of the action-adventure comedy series co-created by Stan Lee as one of his final projects. He also serves as co-producer, along with China's Alibaba Group (BABA), Stan Lee's POW! Entertainment, and Schwarzenegger's Oak Productions. Co-creator of Deadpool, Fabian Nicieza has developed the series, with scripting by Steven Banks. Landis has also joined Genius Brands' development team to help create a live-action series and feature film spin-off of Stan Lee's Superhero Kindergarten. Stan Lee's Superhero Kindergarten will debut on Genius Brands' recently-launched Kartoon Channel! in Q1 2021. It will also be broadcast on Amazon Prime in the U.S., and Alibaba in China on its video streaming platform for kids, Youku. Concurrently, Genius Brands is actively marketing a full-scale global consumer products retail program anchored with toys, publishing, and apparel.
SBLK

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08:42 EDT Star Bulk Carriers provides details on delisting process from OSE - Star Bulk Carriers Corp. refers to the press release of June 4, 2020 announcing the delisting of the Company's common shares from the Oslo Bors. The last day of trading on the Oslo Bors will be July 31, 2020 and the delisting will take effect as from August 3, 2020. The Company's common shares will continue to trade on the Nasdaq Global Select Market under the symbol "SBLK". As a result of the delisting from OSE, the Company will also terminate the registration of its common shares with the Norwegian Central Securities Depository. The termination will take effect following a transitional period, of approximately nine months, from the time of delisting. Star Bulk shareholders that currently have their shares registered in the VPS, whether individuals, entities, brokers or custodians, may elect to transfer their shareholdings to the United States prior to the expiration of the Transitional Period, to facilitate trading on Nasdaq. Such shareholdings may be held through a U.S. broker dealer or recorded directly in the shareholder's name on the Company's share register maintained by the Company's transfer agent, American Stock Transfer and Trust Company. In order to complete this transfer, shareholders should contact their broker or custodian directly. Any Star Bulk shareholders who still have shares registered in the VPS, as of 3 August 2020, will receive a letter with further information on the deregistration of the Company's shares from the VPS. Shares that have not been transferred prior to the expiration of the Transitional Period, will be automatically removed from the VPS, on or about April 30, 2021, and be recorded in book entry form directly in the shareholder's name on the Company's share register maintained by AST. A statement, relating to each such shareholder's account, will be generated and mailed by AST. Additional information may be required from AST.
ENLV

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08:40 EDT Enlivex receives notice of allowance for ALLOCETRA patent application - Enlivex Therapeutics announced that the Japan Patent Office has issued a notice of allowance for a patent application covering ALLOCETRA, the company's immunotherapy product candidate. Upon issuance, the new patent will provide additional intellectual property protection around methods of using ALLOCETRA and pharmaceutical compositions comprising the same. The company expects the new patent to issue in Japan during the third quarter of 2020.
OMAB

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08:39 EDT OMA postpones Anual General Ordinary, Extraordinary Shareholders' Meeting - Grupo Aeroportuario del Centro Norte, S.A.B. de C.V., known as OMA announces that given the prevailing conditions related to the SARS-CoV2 virus that do not guarantee the health of the participants at the Annual General Ordinary and the Extraordinary Shareholders' Meeting, which was scheduled to be held on June 19, 2020, the Meeting has been postponed. The new date of the Meeting will be duly informed on a timely manner.
DBI

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08:38 EDT Designer Brands hopes to have nearly all NA stores open by end of June
ALGN

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08:38 EDT Align Technology announces partnership with MedTech Innovator - Align Technology announced its partnership with MedTech Innovator. MedTech Innovator matches healthcare industry leaders with innovative medtech startups for mentorship and support. In 2020, MedTech Innovator will select 20 startups to participate in its Asia Pacific Showcase program and will award more than $300,000 in cash prizes, scholarships, and in-kind services to its participants. Align Technology will work with MedTech Innovator Asia Pacific to mentor and foster the growth of promising early to mid-stage companies selected for the 2020 Showcase program and provide financial support to MedTech Innovator.
MDT HNHPF

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08:37 EDT Medtronic, Foxconn partner to increase ventilator production - Medtronic (MDT) and Foxconn Industrial Internet (HNHPF) announced that Foxconn has successfully completed Medtronic's regulatory and quality requirements necessary to begin manufacturing Medtronic Puritan Bennett 560 ventilators for Medtronic in the United States. Medtronic and Foxconn are currently ramping up plans to produce 10,000 PB560 ventilators over the next year at Foxconn's Wisconn Valley Science and Technology Park in Mount Pleasant, Wis. The ventilators will be marketed and sold by Medtronic. The two companies connected after Medtronic publicly shared the design specifications for the PB560 through the Medtronic ventilator open source initiative, which launched earlier this year. This effort allows global participants to evaluate options for rapid ventilator manufacturing at scale to help doctors treat patients fighting COVID-19. To date, there have been more than 200,000 registrations for the design specifications at Medtronic.com/openventilator. To respond to global demand, if needed, Medtronic and Foxconn can increase their production capability to more than double the current Foxconn ventilator commitment.
DBI

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08:36 EDT Designer Brands saw meaningful deterioration in store traffic starting on Mar. 6 - Comments taken from Q1 earnings conference call.
ALTG

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08:36 EDT Alta Equipment Group to acquire Hilo Equipment & Services, terms undisclosed - Alta Equipment Group announced that it has entered into a definitive agreement to acquire Hilo Equipment & Services, a privately held distributor of material handling equipment with three branches in the New York City metro area. Hilo sells new and used material handling equipment, partnering with manufacturers including Hyster-Yale Group, Kelley and JLG, and offers repairs and maintenance. Hilo generated approximately $50M in revenue and had adjusted EBITDA of approximately $3M in FY19. Terms of the acquisition were not disclosed. The transaction is expected to close in early Q3, subject to customary conditions.
POAI

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08:34 EDT Predictive Oncology's TumorGenesis division secures commercial sale - Predictive Oncology announces that Predictive's TumorGenesis division sold its first order of its unique ovarian cancer cell culture media for cancer cells collected from patient derived samples through its distributor US Biological Corporation. The media used to grow the novel and unique ovarian cancer cell lines, licensed by TumorGenesis and its partner, GLG Pharma are able to retain 95%+ of the DNA and RNA as well as crucial proteomic signatures. The media was sold to a top rated medical university in the New England area for research in isolating and growing ovarian cancer cells from the fluid often found in the abdomen of women with advanced ovarian cancer, called the 'ascites' fluid. Ovarian cancer cell culturing from ascites fluids are notoriously difficult using standard media mixes often prone to failure and cell lines that are not representative of the patient's ovarian cancer.
SRPT SELB

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08:33 EDT Sarepta, Selecta Biosciences enter into research license, option agreement - Sarepta Therapeutics (SRPT) and Selecta Biosciences (SELB) announced that they have entered into a Research License and Option agreement granting Sarepta an option to license the rights to develop and commercialize Selecta's immune tolerance platform, ImmTOR, for use in Duchenne muscular dystrophy and certain limb-girdle muscular dystrophies. In advance of exercising its option, Sarepta will conduct research and evaluate the utility of ImmTOR to minimize or prevent the formation of neutralizing antibodies to adeno-associated virus in connection with the administration of Sarepta's DMD and LGMD gene therapy candidates. Sarepta's late-stage gene therapy candidates are delivered using AAV - in particular, AAVrh74. AAVrh74 was selected because of its safety profile, superior muscle tropism, empirical demonstration of high expression, and low screen-out rate for pre-existing antibodies. Currently, however, all systemic AAV-delivered constructs are one-time therapies that cannot be re-dosed due to the robust post-administration development of NAbs specific to the AAV vector. Selecta is a leader in immune tolerance and has generated strong preclinical evidence to support the potential for re-dosing patients receiving gene therapy. Selecta has reported that in preclinical studies, when used in combination with AAV gene therapy vectors, Selecta's ImmTOR immune tolerance platform inhibits the development of NAbs to the vector, permitting re-dosing of the gene therapy. Under the terms of the research license and option agreement, Sarepta will make an initial payment to Selecta, and Selecta is eligible to receive certain pre-clinical milestone fees. If Sarepta exercises its options to enter any commercial license agreements, Selecta will be eligible for additional development, regulatory, and commercial milestone payments, as well as tiered royalties on net product sales. Additional financial details are not being disclosed.
FBRX

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08:33 EDT First Brand Coporation issued new U.S. patent - Forte Biosciences announced the issuance of its seventh U.S. patent, broadening protection to include methods for culturing gram negative bacteria from the skin. Forte said in a release, "Together with the six U.S. patents previously issued, Forte now has extensive patent protection covering the composition and method of use of our technology focused on inflammatory skin conditions."
ALPN

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08:30 EDT Alpine Immune Sciences Inc trading resumes
ENPH

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08:24 EDT Enphase jumps 10% to $43.20 after short report brings analyst defenses
TEVA

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08:23 EDT Teva announces new Ajovy data from FOCUS study - Teva announced new data examining quality of life, health status, depressive symptoms, work productivity and activity impairment of patients treated with Ajovy during the 12-week open-label extension of the Phase IIIb FOCUS study. An additional analysis of pooled results from three Ajovy Phase III trials examined headache- and migraine-related disability based on guidelines set forth by the American Headache Society. The data were presented at the AHS Virtual Annual Scientific Meeting. The following results were observed in quality of life, health status, depressive symptoms, and work productivity based on scores from validated patient-reported questionnaires, including Migraine-Specific Quality of Life, or MSQoL, 5-level EuroQol-5 Dimension, or EQ-5D-5L, Patient Global Impression of Change, or PGIC, 9-item Patient Health Questionnaire, or PHQ-9 and Work Productivity and Activity Impairment, or WPAI, questionnaire. MSQoL quality-of-life domain scores and the EQ-5D-5L health status score at the end of the double-blind period and through the end of the open-label extension. The proportion of patients who experienced a response on the PGIC increased from 58% to 64% at the end of the double-blind period to 75% to 77% at the end of the open-label extension. Depressive symptom scores were reduced by 1.6 to 2.4 points by the end of the open-label extension. Overall, 14.5% to 20% reductions from baseline were reported in overall health-related work impairment by the end of the open-label extension. Additionally, the safety and tolerability of Ajovy during this open-label extension was evaluated, with the most common adverse events, or AEs, being injection-site reactions, such as injection-site erythema. The reports of AEs leading to discontinuation were less than 1% and 3% for serious AEs. The AHS Consensus Statement provides guidelines on determining response to CGRP pathway targeted treatments for migraine. As changes in migraine frequency may not adequately assess treatment benefit in all patients, these guidelines recommended specific improvements in disability scores on the MIDAS and HIT-6 that would be considered clinically meaningful and evidence of response to treatment. The disability in patients treated with Ajovy was evaluated using pooled data from the three double-blind Phase III trials. A post-hoc analysis of the pooled Phase III study data based on guidelines set forth by the Consensus Statement noted Ajovy patients experiencing severe disability due to migraine at baseline achieved the following disability score reductions: For patients with a baseline MIDAS score of 11-20, the proportion of patients achieving a 5-point reduction from their baseline score was 71% and 70% with Ajovy and 49% with placebo. The proportion of patients with a baseline MIDAS score of greater than 20 who achieved a 0% reduction in points was 69% and 79% with AJOVY and 58% with placebo. The proportion of patients achieving a 5-point reduction from baseline in HIT-6 scores was 53% and 55% with Ajovy and 39% with placebo.
BRP

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08:22 EDT BRP Group upsizes senior revolving credit facility to $400M - BRP Group announced that its subsidiary, Baldwin Risk Partners, has amended its senior revolving credit facility, effective immediately, to increase the committed line under the credit facility to $400M, up $100M from its previous amount of $300M. As part of the expanded credit facility, Capital One joined the group of original lenders as a co-documentation agent. The bank group is led by JPMorgan as sole bookrunner, lead arranger, administrative agent and lender, Wells Fargo and Bank of America as co-syndication agents, Cadence Bank as the other co-documentation agent and Wintrust Financial. Each of the original lenders is maintaining or increasing its commitment under the revolving credit facility. There was no change to interest rates, as borrowings under the amended credit facility accrue interest on amounts drawn at LIBOR plus 200 basis points to LIBOR plus 300 bps based on BRP LLC's total net leverage ratio. The maturity date of the revolver remains September 23, 2024.
FSLR DOW

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08:21 EDT First Solar signs 15-year power purchase agreement with Dow Inc. - First Solar (FSLR) announced that it had signed a 15-year power purchase agreement with Dow, Inc. (DOW) for its Gulf Coast operations. Dow's Texas Operations is the largest petrochemical site in the western hemisphere. First Solar had previously disclosed the execution of the PPA without identifying the offtaker. Under the agreement, First Solar will supply Dow with renewable energy from 75 percent of its 200-megawatt AC Horizon Solar project in Frio County, Texas. The project will utilize First Solar's high-performance, eco-efficient Series 6 photovoltaic modules, designed and developed at the Company's research and development centers in California and Ohio. The Series 6 modules that will power the project utilize a range of advanced technologies, including ENGAGE PV Polyolefin Elastomers by Dow, which are used as encapsulant films to enhance the module's performance and efficiency.
PRAH

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08:19 EDT PRA Health prepares to navigate RACE Act requirements - The company said, "Between 2007-2017, 78 novel adult cancer agents were approved by the U.S. Food and Drug Administration, but none of those drugs were researched to determine effectiveness for pediatric cancers. That is about to change on August 18 when the RACE Act - The Research to Accelerate Cures and Equity for Children Act - goes into effect. Passed in 2017, the RACE Act amends the existing PREA - Pediatric Research Equity Act - and eliminates the exemption from PREA requirements for cancer drugs that have orphan status. The new law requires pediatric evaluation of new drugs and biologics intended for the treatment of adult cancers and directed at a molecular target substantially relevant to the growth or progression of pediatric cancer. Clinical research companies and their pediatric research specialists, including PRA Health Sciences, will be called on to support pharmaceutical and biotech companies as they sponsor the required research for pediatric oncology indications. PRA's Center for Pediatric Clinical Development and the team working on the RACE Act implementation include Dr. Sorrentino as well as Dr. Martine Dehlinger-Kremer, VP, Scientific Affairs, Pediatric Subject Matter Expert; Dr. Jacqui Whiteway, Senior Pediatric Strategy Liaison; Jo Dewhurst, LLB Dip; and Missy Hansen, MSN, APRN, CNP-Pediatrics, Pediatric Strategy Liaison. Together, with the addition of dozens of other PRA researchers and pediatric specialists, this designated team of experts is ready to utilize their collective experience in pediatric clinical development to support RACE Act-focused initiatives. "
LCTX

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08:17 EDT Lineage Cell Therapeutics reinitiates patient enrollment in OpRegen study - Lineage Cell Therapeutics announced that it has restarted patient enrollment in a Phase 1/2a clinical study of its lead product candidate, OpRegen, a retinal pigment epithelium, or RPE, cell transplant therapy currently in development for the treatment of dry age-related macular degeneration, or AMD, following a temporary pause in enrollment as a result of the COVID-19 pandemic. The company said in a release, "The first patient dosed in the re-start was at Cincinnati Eye Institute, or CEI, under the direction of principal investigator Christopher D. Riemann, M.D., Vitreoretinal Surgeon and Fellowship Director, CEI and University of Cincinnati School of Medicine. CEI is a global leader in ophthalmology research and a clinical site where local health and safety regulations recently enabled and cleared clinical study recruitment and treatment. The patient enrolled at CEI was administered Lineage's new thaw-and-inject formulation of OpRegen with Gyroscope Therapeutics' Orbit Subretinal Delivery System. The Company anticipates that it will complete enrollment of the last 3 patients in Cohort 4 of the OpRegen clinical study in the third quarter of 2020."
TFII

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08:17 EDT TFI International completes acquisition of Gusgo Transport - TFI International announced that it has closed on the previously announced acquisition of privately held Gusgo Transport, a container transport and storage company operating out of Vaughan, Ontario. As stated previously, the acquired business will become part of TFI International's Truckload segment.
BNGO

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08:16 EDT Bionano Genomics amends proxy statement for Annual Meeting - Bionano Genomics announced that on June 17, 2020 it filed an amendment to its Proxy Statement for its 2020 Annual Meeting of Stockholders in order to amend and supplement Proposal 1 in the Proxy Statement. Pursuant to Proposal 1, Bionano is submitting to its stockholders for approval a series of alternate amendments to its Amended and Restated Certificate of Incorporation, to effect, at the discretion of the Board of Directors: a reverse split of Bionano's common stock in the range of 1-for-10 to 1-for-20; and for such reverse stock split in the range of 1-for-10 to 1-for-20, a reduction in the number of authorized shares of common stock from 200,000,000 to a number ranging from 40,000,000 to 20,000,000 shares, respectively. The Proxy Statement originally stated that the effectiveness or abandonment of any of the amendments described above will be determined by the Board of Directors prior to an outside date of July 31, 2020. Pursuant to the amendment, this outside date was extended to June 25, 2021. This extension allows the Board of Directors additional time to evaluate whether to effect or abandon any of the reverse split and corresponding authorized share reduction amendments described above.
ALPN ABBV

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08:15 EDT Alpine Immune Sciences, AbbVie announce exclusive license agreement for ALPN-101 - Alpine Immune Sciences (ALPN) and AbbVie (ABBV) announced an exclusive worldwide option and license agreement for ALPN-101, a dual CD28/ICOS costimulation antagonist. CD28 and ICOS are costimulatory molecules that likely play roles in multiple autoimmune and inflammatory diseases. ALPN-101 is a potent inhibitor of both CD28 and ICOS pathways with demonstrated efficacy in multiple preclinical disease models, superior to blockade of either pathway alone. Favorable safety and tolerability, pharmacokinetics and pharmacodynamics have been observed in a first-in-human study in adult healthy volunteers. Under the terms of the agreement, Alpine will receive an upfront payment of $60M, and will also be eligible to receive up to an aggregate of $805M for exercise of the option and success-based development, regulatory and commercial milestones. In addition, Alpine is eligible to receive tiered royalties on net sales of ALPN-101. In exchange, AbbVie will receive an option to an exclusive license for ALPN-101. During the option period, Alpine will conduct a phase 2 study in systemic lupus erythematosus. Upon exercise of the option, AbbVie will conduct all future clinical development, manufacturing and commercialization activities for ALPN-101.
TRU

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08:15 EDT TransUnion launches CreditVision Acute Relief Suite - TransUnion officially launched its CreditVision Acute Relief Suite to assist lenders and insurers in supporting consumers while still managing risk within their portfolio. The CreditVision Acute Relief Suite features a set of 88 attributes that identify accounts and relationships receiving special accommodations for consumers currently in relief status. The attributes allow lenders and insurers to better understand how consumers and their accounts have been affected - broken out by different credit products, the timing of when they were reported in these statuses and the balances of those accounts.
GENE

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08:14 EDT Genetic Technologies granted U.S. patent for risk test - Genetic Technologies announced the issuance of US Patent No: US 10,683,549, Methods for assessing risk of developing breast cancer. Genetic Technologies is the first company to successfully commercialise a polygenic risk test for breast cancer in the world. The granted patent covers our proprietary panels of single nucleotide polymorphisms and the combination of clinical and phenotypic risk models to create the most comprehensive risk assessment tool on the market: GeneType for Breast Cancer. The proprietary technology incorporated into GeneType for Breast Cancer provides significant benefits over existing breast cancer risk assessment algorithms. Breast cancer is often looked at as an inheritable disease, but about 85% of breast cancer patients do not have a strong family history of breast cancer. Combining clinical risk factors and GTG's patented phenotypic risk model can identify those who are at high, average or low risk of developing breast cancer, which can inform an individual's personalised preventative protocol alongside physicians.
DSKE

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08:12 EDT Daseke expects positive cash flows from operating activities, FCF in Q2 - Daseke provided an update on its business, operations and strong liquidity position as of June 1, 2020. Freight volumes have improved five of the last six weeks since troughing during the month of April. Company expects positive cash flows from operating activities and positive Free Cash Flow in the second quarter ending June 30, 2020. At June 1, 2020 the Company had more than $220M of available liquidity, including approximately $80M available under the revolving credit facility and cash and cash equivalents. Cash and cash equivalents as of June 1, 2020 increased to over $140M compared to $107.5M at the end of the first quarter. Financial results continue to benefit from the previously launched integration, business improvement and comprehensive restructuring plans, which have strengthened the Company and continued to support positive operating profits and free cash flow generation. Daseke has made substantial progress on the strategic divestiture of its Aveda assets and expects to conclude the process by the end of the third quarter 2020. "As the leader in the North American flatbed and specialized transportation market, Daseke continues to move the industrial economy as many of the companies in the end markets we serve are essential service providers and critical components to the economy," said Chris Easter, CEO of Daseke. "Our business model remains stable and resilient, supported by a highly diverse, blue-chip customer base and a substantial asset-light business, which brings a highly variable cost structure. Further, the proactive efforts we've taken over the last year to streamline our operations and improve our business flexibility have helped Daseke generate positive free cash flow and drive further operational and cost efficiencies, despite the headwinds to volumes related to the pandemic during the quarter. Additionally, excluding the Memorial holiday week, we've seen sequential volume improvements for five straight weeks across the month of May and the beginning of June. We will remain agile and adaptive to changes in the environment, as we continue to deliver on our goals to improve operating income results and consistently grow our cash flows. Lastly, we've made substantial progress in the strategic divestiture of our Aveda assets, which focus primarily on the oil & gas end market. We expect to complete the process by the end of the third quarter, at which time our exposure to the oil & gas end market will fall from approximately 13% of revenue in 2019, to less than 2% moving forward. More importantly, we will have further streamlined our business from 16 operating companies at this time last year, to 9 following completion of the process. We have materially transformed our business and are well positioned to drive improved operating performance and long-term growth as the U.S. economy continues to build momentum and recover from the pandemic."
DNK

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08:09 EDT Phoenix Tree appoints Yan Cui as interim CEO - Phoenix Tree announced updates to its board of directors and senior management team. Yan Cui, a co-founder, director and president of the company, has been appointed by the board as interim CEO with immediate effect. Cui has been responsible for the management and operations of the company, together with Jing Gao, a co-founder, director and CEO of the company, since it was founded five years ago. Gao is currently involved in an investigation by local government authorities into certain matters relating to his business venture prior to the founding of Danke, and thus is not able to attend to the company's business or perform any of his directorial and managerial roles at the company. The company has no plausible reason to believe that the investigation Gao is involved in relates to or results from any business activities or other dealings of the company. The company currently does not expect the absence of Gao to have any material adverse impact on its daily business operations, and will continue to assess the situation and make transitional arrangements if necessary.
XERS

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08:09 EDT Xeris Pharmaceuticals announces topline results from XP-3924 study - Xeris Pharmaceuticals announced topline results from a proof-of-concept Phase 2 study of a novel Xerisol pramlintide-insulin co-formulation, or XP-3924, in adults with type 1 diabetes mellitus. XP-3924 is designed to improve the synergistic combination of two therapies: pramlintide and insulin. The separate administration of these existing therapies in combination reduces both post-prandial glucose excursions and glucose variability, as well as improves overall glycemic control. A pramlintide-insulin co-formulation may help reduce the daily burden associated with pramlintide co-administration. This reduction in the multiple injection burden using XP-3924 may also improve longer term pramlintide treatment adherence and persistency. The completed Phase 2 study was a randomized, open-label, active comparator-controlled, three-period cross-over study, which enrolled 18 adult participants with type 1 diabetes. This study aimed to investigate the pharmacokinetics, pharmacodynamics, and the safety and tolerability of a single dose of XP-3924. Subjects were randomly allocated to a sequence of three treatments: XP-3924, regular insulin, or regular insulin plus pramlintide co-administered as separate injections. The study drugs were administered subcutaneously before the intake of a standardized 75-gram oral glucose challenge. The subjects' blood glucose levels were monitored for 6 hours after drug dosing. Treatment with XP-3924 resulted in a 62.3% reduction of hyperglycemia after the glucose challenge when compared to Humulin. Additionally, XP-3924 exhibited comparable postprandial glycemic control to that of the co-administered injections of Humulin and Symlin. The mean absolute change in blood glucose was less in XP-3924 when compared to both Humulin and co-administered injections of Humulin and Symlin after the oral glucose challenge. The glucose variability after treatment with XP-3924 was less than both Humulin and co-administered injections of Humulin and Symlin, as defined by the comparison of the coefficient of variation of all plasma glucose readings across the sjx-hour duration of study treatments. The incidence and severity of treatment emergent adverse events was comparable across all treatment arms, as were the overall number of hypoglycemic events during dosing visits. There were minimal gastrointestinal side-effects reported in any treatment arm. There was a comparable incidence of injection site reactions and no edema was noted, across all treatment arms. XP-3924 was safe and well tolerated, and no serious adverse events occurred in this study.
VMD

Hot Stocks

08:09 EDT Viemed Healthcare to join Russell 3000 Index - Viemed Healthcare announced that it expects to join the broad-market Russell 3000 Index at the conclusion of the 2020 Russell indexes annual reconstitution, effective after the US market opens on June 29, 2020 according to a preliminary list of additions posted June 5, 2020.
LLY

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08:08 EDT Eli Lilly begins Phase 3 trial with baricitinib in COVID-19 patients - Eli Lilly and Company announced that the first patient has been enrolled in a Phase 3 randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of baricitinib, an oral JAK1/JAK2 inhibitor licensed from Incyte, in hospitalized adults with COVID-19. Baricitinib, marketed as OLUMIANT, is approved in 70 countries as a treatment for adults with moderately to severely active rheumatoid arthritis. Lilly expects to enroll 400 patients in the trial, with data expected in the next few months. The study will be conducted in the U.S., Europe and Latin America and includes patients hospitalized with SARS-CoV-2 infection who have at least one elevated marker of inflammation but do not require invasive mechanical ventilation at study entry. In COVID-19 infection, increased disease severity can be associated with a hyperinflammatory state. It is hypothesized that through JAK1 and JAK2 inhibition, baricitinib may reduce the cytokine storm associated with the complications of this infection. In addition, baricitinib may have a role in inhibiting the host cell proteins that assist in viral reproduction, reducing the ability of infected cells to make more virus. A manuscript detailing this mechanism of action of baricitinib in COVID-19 has been accepted for publication by EMBO Molecular Medicine. The primary endpoint for Lilly's study is the proportion of patients who die or require non-invasive ventilation/high-flow oxygen or invasive mechanical ventilation by Day 28 in patients treated with 4 mg of baricitinib daily compared to placebo. Patients will receive baricitinib or placebo for up to 14 days or until discharge from the hospital. Key secondary outcomes of this study include the proportion of patients with clinical improvement at different time points, time to recovery, duration of hospitalization, number of ventilator-free days and mortality over a 28-day period. The data from Lilly's trial will complement data from the study of baricitinib with remdesivir in the second phase of the Adaptive COVID-19 Treatment Trial run by the National Institute of Allergy and Infectious Diseases, part of the National Institutes of Health. This study - which enrolled its first patient last month - assesses the efficacy and safety of the combination of a 4 mg daily dose of baricitinib plus remdesivir, compared to remdesivir. Lilly is also supporting select ongoing multisite and single-site investigator-initiated trials in Europe and North America for hospitalized patients with COVID-19 infections, including a trial in Nova Scotia, Canada. The trial is an independent 4-arm Phase 2 study, measuring investigational medications, including baricitinib, as adjuncts to clinical standard of care treatment to evaluate the safety and effectiveness of anti-COVID-19 treatment. These studies by academic and government institutions will provide information on hundreds of additional patients treated with baricitinib and either placebo or active comparators.
DAL

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08:06 EDT Delta Air Lines sees domestic capacity down 55%-60% y/y in August
VZ CSCO

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08:06 EDT Verizon expands Virtual Network Services portfolio with Cisco's ENCS - Verizon Business (VZ) is expanding its Virtual Network Services portfolio for enterprise customers with the introduction of Cisco's (CSCO) 5000 Series Enterprise Network Compute System. The Cisco ENCS purpose-built platform will now be included within Verizon's catalog of virtual network functions and service chains that are offered to customers.
DAL

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08:06 EDT Delta Air Lines sees daily cash burn $30M/day by end of June, CEO Bastian says
UROV

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08:06 EDT Urovant Sciences announces collaboration with Sunovion Pharmaceuticals - Urovant Sciences announced it has entered into an exclusive three-year distribution agreement with Sunovion Pharmaceuticals for services to support the commercialization of vibegron, an investigational agent for the treatment of overactive bladder. Both companies are subsidiaries of Sumitomo Dainippon Pharma. Urovant said in a release, "The co-promotion agreement will enable Urovant to leverage Sunovion's commercial infrastructure to increase efficiency of the planned launch of vibegron. The agreement covers services such as account management, contract operations, third party logistics, and trade and retail distribution."
DAL

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08:05 EDT Delta Air Lines: 500 workers diagnosed with coronavirus
DAL

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08:05 EDT Delta Air Lines to decide on additional aircraft retirements before year-end - Comments taken from Delta's Annual Meeting of Shareholders.
RKDA

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08:05 EDT Arcadia Biosciences gets patents covering herbicide tolerance in wheat - Arcadia Biosciences announced the Australia Patent Office has granted the company a foundational patent covering herbicide tolerance in wheat. Patent Number 2016288257 grants intellectual property protection for mutations to the wheat genome to make it herbicide tolerant. The company also received a U.S. Notice of Allowance 15/740,876 from the U.S. Patent and Trademark Office for the same technology. Australia and the United States are the first major wheat-producing countries to approve the patents, with additional patents pending in other key wheat markets.
SCOR

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08:04 EDT Comscore and Rockfleet Broadcasting renew TV measurement agreement - Comscore announced a renewal agreement to provide Rockfleet Broadcasting with continued TV measurement in the Bangor, ME and Wausau, WI markets.
FEYE

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08:04 EDT FireEye appoints Brad Maiorino as Chief Strategy Officer - FireEye announced the appointment of Brad Maiorino as Chief Strategy Officer, reporting to FireEye CEO Kevin Mandia. FireEye said in a release, "As Chief Strategy Officer at FireEye, Maiorino will play a key role in influencing the FireEye & Mandiant product and solutions strategy based on customer needs. Maiorino will also work with FireEye customers to deploy cybersecurity and risk management solutions to combat today's dynamic threat environment. Prior to joining FireEye, Maiorino most recently served as Chief Information Security Officer for Thomson Reuters."
AMS

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08:04 EDT American Shared Hospital acquires Gamma Knife Center Ecaudor for $2M - American Shared Hospital announced that its 81% owned subsidiary, GK Financing, has completed the acquisition of approximately 98% of the total outstanding shares of Gamma Knife Center Ecuador purchased from GKC Ecuador's majority shareholders Global Medical Investments GMI AB, Scandinavian Care Investments AB, and Brock Investment Limited. At a later date, AMS plans to acquire the remaining outstanding shares of GKC Ecuador by entering into a separate stock purchase agreement with the remaining minority shareholders of GKC Ecuador. The total purchase price for the Acquisition, including acquisition of the minority shares is expected to be approximately $2M, or about 1x historical annual revenue of GKC Ecuador. This purchase price has been paid with $575,000 in cash and a $1.425M loan from the United States International Development Finance Corporation. The purchase price is subject to certain post-closing adjustments, including adjustment for GKC Ecuador's working capital and excess cash. The DFC loan is denominated in U.S. dollars, which is also the currency of Ecuador. GKC Ecuador is a well-established Gamma Knife operation founded in 2009 as a private clinic to introduce advanced stereotactic radiosurgery into Ecuador. GKC Ecuador's center is located in Ecuador's largest city, Guayaquil, which has a population of nearly 2.5 million people. Ecuador has a total population of approximately 16 million people. Sixty, or 30%, of the approximately 200 neurosurgeons practicing in Ecuador have referred patients to the center, which has treated over 1,400 patients to date. GKC Ecuador currently operates a Leksell Gamma Knife model 4C which is under contract to be upgraded to a Gamma Knife Perfexion. The Perfexion is expected to be installed in late 2020 or early 2021. The Perfexion system allows for greater ease of use, faster treatment times and can treat a wider range of anatomical structures, all of which can drive higher patient volume.
ACN

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08:03 EDT Accenture subsidiary awarded position on up to $50M BPA - Accenture Federal Services, a subsidiary of Accenture, has been awarded a position on the U.S. Patent and Trademark Office, or USPTO, Intelligent Automation and Innovation Support Services , or AISS, blanket purchase agreement, or BPA, a multi-award contract vehicle. The five-year BPA is valued at up to $50M. The scope of the work includes piloting, testing and implementing advanced technologies such as intelligent automation, artificial intelligence, microservices, machine learning, natural language processing, robotic process automation and blockchain.
YGYI

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08:02 EDT Youngevity's CLR Roasters signs five-year contract with H&H Coffee Group Export - Youngevity announced that its wholly-owned subsidiary, CLR Roasters, has signed a five-year contract with H&H Coffee Group Export Corp.to sell CLR's espresso brands, Cafe La Rica and Cafe Cachita into Panama. Terms are C.O.D. and F.O.B. Miami, with the initial order of approximately 60,000 units of Cafe Cachita Espresso bricks expected to ship this week, and a second order of the brand Cafe La Rica of the same amount planned within 14 days thereafter. The distribution relationship establishes minimum order quantities of 40-foot containers per order and is expected to result in annual revenue of approximately $2M.
CNTY

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08:02 EDT Century Casinos reopens its two casinos in Colorado - Century Casinos announced that operations at Century Casino & Hotel Cripple Creek resumed on June 15 and at Century Casino & Hotel Central City on June 17. Prior to reopening, Century Casinos implemented comprehensive and Colorado specific safety and social distancing protocols at the properties.
QUOT

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08:01 EDT Quotient Technology enters partnership with Mandlik & Rhodes - Quotient announced a partnership with Mandlik & Rhodes. Quotient said in a release, "Through this partnership, Quotient offers CPG brands significant cost savings over legacy coupon clearing firms for the clearing of digital coupons without transition or laborious integration costs through the use of Mandlik & Rhodes' coupon clearing service. Retailers will continue to be paid as they traditionally have for clearing services. As digital couponing has grown, the legacy coupon clearing industry has failed to transform and take advantage of the efficiencies that technology brings to other industries - ultimately lowering the cost to serve. With this partnership, CPGs can immediately benefit from a lower cost to process digital coupons - freeing up more working dollars and increasing the ROI of their overall marketing spend. Additionally, they benefit from a fully transparent model for delivering coupon clearing services so that every cost is clear. As a result of this partnership, CPGs will be able to spend less on clearing fees today while saving even more as the shift from legacy offline print to digital coupons accelerates. And, they will be able to do so with the confidence that they won't be nickel and dimed on hidden processing charges or ancillary fees. CPGs will also no longer need to be concerned about fraud fees for digital coupons, since the risk of fraud is significantly reduced in a well-structured digital coupon environment. Quotient's Retailer iQ digital coupon platform is designed with this in mind, with multiple checks and balances that maintain the integrity of Quotient's platform. Zero instances of fraud have been reported using Retailer iQ."
LXXGF

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07:59 EDT Lexagene Holdings provides status update on COVID-19 testing - LexaGene Holdings provides a status update on the previously announced placement of its pre-commercial LX Analyzer. The instrument the Company placed in a major US hospital laboratory was configured to screen for COVID-19 and seven other respiratory pathogens. LexaGene's technology performs highly multiplex RT-PCR, which is a gold-standard chemistry that provides exceptional sensitivity and specificity. LexaGene has automated the entire workflow in an instrument designed to be placed at the point-of-need. It takes less than 1 minute of hands-on time to initiate sample processing for walk-away testing. Regarding the Company's FDA plans, LexaGene has recently received comments back on its submitted plan for Emergency Use Authorization for COVID-19 testing. Since submitting the application, the FDA has updated its template for manufacturers, changing some requirements. The Company has amended its plan and is now awaiting further communication from the FDA, which it anticipates soon. Until proposed studies are completed, and the FDA grants LexaGene's instrument EUA for COVID-19 testing, all work using LexaGene instruments is classified as "Research Use Only" which is standard for the industry. The Company is not making any express or implied claims that its product has the ability to eliminate, cure or contain COVID-19 at this time.
APTX

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07:57 EDT Aptinyx completes enrollment in Phase 2 exploratory study of NYX-783 - Aptinyx announced the completion of enrollment in its ongoing Phase 2 exploratory study of NYX-783 to evaluate the safety and efficacy of NYX-783 in patients with post-traumatic stress disorder. The company anticipates reporting data from the study in late 2020.
ALPN

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07:57 EDT Alpine Immune Sciences Inc trading halted, news pending
WDDMF

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07:56 EDT WeedMD terminates Nomination Agreement with Keith Merker, Michael Kraft - WeedMD also announced that the nomination rights and voting agreement entered into between WeedMD, Keith Merker, former CEO and board member of WeedMD, and Michael Kraft, former Chairman of WeedMD, dated December 20, 2019 has been mutually terminated effective immediately. Pursuant to the terms of a termination agreement entered into by the parties, the Nomination Agreement is of no further force and effect and no nomination or other rights remain effective thereunder.
WDDMF

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07:55 EDT WeedMD launches same-day medical cannabis delivery service - WeedMD announced the launch of its same-day medical cannabis home delivery service. The pilot project called 'PatientDirect' will service local patients in the greater Toronto-area starting in June, with order fulfillment from the Company's Bowmanville, Ontario distribution centre located just outside Toronto. PatientDirect is intended to ease potential third-party postal and delivery service disruptions resulting from the current business conditions. The service will be offered to new and existing Starseed Medicinal patients commencing in June with eligible patients being notified by email. The service will expand to WeedMD patients in the coming weeks. Over time it is expected to become a standard service option. While the delivery service will cover the greater Toronto region at launch, WeedMD expects to expand the delivery zone in southwestern Ontario by working closely with logistics partner Prime Time Messenger Inc. Patients with eligible Ontario postal codes from Bowmanville to Mississauga, and north up to Aurora can select the same-day delivery option following order confirmation at the time of checkout. Orders with applicable limits will be provided the service free of charge or on par with Canada Post rates if minimum orders not met.
DTMXF

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07:54 EDT Datametrex reports C$1.5M sales from COVID-19 test kits - Datametrex AI shared a corporate update that since announcing on April 16, 2020, that it secured the rights to import and sell high-quality South Korean manufactured Nucleic Acid COVID-19 test kits. The Company has sold approximately 30,000 test kits and 7 PCR machines to several Canadian companies, for total gross sales of approximately C$1.5M. Datametrex has little or no upfront costs associated with the sale of these test kits. Since May 15th, Datametrex has generated gross sales of $500,000 with the sale of 10,000 test kits and one PCR machine to a large Canadian mining company with operations in West Africa. Since June 8th, Datametrex has sold $810,000 with initial orders comprising of 12,000 test kits and six PCR machines to two Canadian companies. On June 9th the Company arranged with lab partner Transpharm Canada to conduct ongoing testing for a private Quebec metal mining company with an initial order of 2,000 test kits generating gross sale of approximately $250,000 for Datametrex. The company said, "The Company's project pipeline is significant on both the COVID-19 test kits and Personal Protective Equipment based on multiple projects in various stages of development across Canada, US, Africa, Asia, Australia and the EU. We are waiting for PO approvals with specified COVID-19 sales and or tender proposal process. The Company will recognize revenue upon sale and shipment of the test kits. The Company will also receive additional revenue streams as we secure new business and continue to provide Ai services, fullfill contracts and or supply agreements to goverments, corporate customers upon fulfillment."
CBIIF

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07:51 EDT CB2 Insights announces amendments to promissory note - CB2 Insights announces that it has amended the terms of its issued and outstanding promissory note held by Merida Capital Partners, which is designed to help the Company achieve its long term growth plans and drive continued profitability. The Company has entered into an amended and restated promissory note, which amends the terms of the promissory note originally issued by the Company on December 20, 2018 and amended on June 2019. Under the terms of the Amended Note, the principal amount of $3 million will become payable on December 24, 2022, carry an annual interest rate of 8%, payable, at the Company's option, either in cash or in common shares of the Company. If interest is paid in common shares, the number of shares will be calculated at a price per share equal to a 10% discount to the 20-day volume-weighted average trading price of the Company's common shares on the Canadian Securities Exchange. Additionally, if at any time prior to the maturity date, the closing price of the Company's common shares on the CSE is equal to or greater than C$0.30 for 20 consecutive trading days, then the outstanding amounts owed under the Amended Note will be converted into that number of common shares obtained by dividing the Canadian dollar equivalent of the sum of the principal amount of $3,000,000 and the unpaid accrued interest owing up to the conversion date, by the volume-weighted average closing price of the Company's common shares on the CSE during such twenty consecutive trading day period, less a discount of 10%. The Amended Note is effective as of April 1, 2020. On an unaudited basis, the Company has achieved its target of reaching positive cash flow and has seen two consecutive months of profitability. As a result of the COVID-19 pandemic, the Company also received $652,500 in government funds for its medical services division in the US. This funding provided the Company with needed cash during the early days of the pandemic. Used within the confines of the program, the Company expects that 100% of this funding will be forgiven. As consideration for the amendments, the Company issued warrants entitling the holder to purchase up to 3 million common shares at an exercise price of C$0.14 per common share during the period commencing on the first anniversary of date of issuance of the warrants and ending three years from such issuance date.
HROW

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07:49 EDT ImprimisRx's Klarity-C formulation available for prescriptions by optometrists - ImprimisRx announced its Klarity-C preservative-free formulation may now be prescribed by Florida's nearly 2,000 optometrists as a result of the Florida Board of Optometry's recent additions to its Formulary of Topical Ocular Pharmaceutical Agents. Klarity-C, which has been prescribed for thousands of Americans in all 50 states, was recently recognized at a Best of Saturday Sessions presentation at the 2020 ASCRS Annual Meeting in a presentation entitled "Efficacy of Topical 0.1% Cyclosporine in Chondroitin Sulfate Ophthalmic Emulsion in Patients with Dry Eye". Klarity-C, which is produced according to the highest federal manufacturing standards at the ImprimisRx FDA-registered outsourcing facility, has been one of ImprimisRx's fastest growing topical formulations.
CPAH

Hot Stocks

07:47 EDT CounterPath regains compliance with Nasdaq listing standard - CounterPath announced that it has received a letter from the NASDAQ Stock Market wherein, based on the Company's Form 8-K, dated June 11, NASDAQ has determined that the Company complies with the Listing Rule 5550(b)(1). CounterPath said in a release, "As previously disclosed, on December 16, 2019, the Company received a letter from the listing qualifications department staff of NASDAQ notifying the Company that the stockholders' equity of $1,922,675, as reported in its Quarterly Report on Form 10-Q for the period ended October 31, 2019, was below the minimum stockholders' equity of $2,500,000. The minimum stockholders' equity of $2,500,000 is required for continued listing on the NASDAQ Capital Market as set forth in NASDAQ listing rule 5550(b)(1), and as of December 13, 2019, the Company did not meet the alternatives of market value of listed securities or net income from continuing operations. As of June 11, 2020, after completion of the $1 million private placement, the Company believes that it has regained compliance with the minimum stockholders' equity requirement as a result of the closing of the Offering. NASDAQ will continue to monitor the Company's ongoing compliance with the minimum stockholders' equity requirement and, if at the time of its next periodic report for the quarter ended July 31, 2020 the Company does not evidence compliance with the minimum stockholders' equity requirement, the Company may be subject to delisting. At that time, NASDAQ Staff will provide written notification to the Company, which it may then appeal Staff's determination to a Hearings Panel. There can be no assurance that the Company will be able to maintain compliance with the minimum stockholders' equity requirement."
J

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07:47 EDT Jacobs, Aurecon Joint Venture providing sewage treatment in Australia - Jacobs, in a joint venture with Aurecon, is delivering sewage treatment planning and design services to Urban Utilities in a three year program. Urban Utilities is a distributor-retailer responsible for delivering vital water and sewage services to households and businesses in South East Queensland, Australia. Urban Utilities manages approximately $3.76B in assets, including 29 sewage treatment plants, and provides water and sewerage services to a population of 1.5 million. Jacobs and Aurecon formed a joint venture, "AJile," to deliver the planning and design services. The project team is co-located with Urban Utilities in its corporate office in Brisbane, Australia.
CAMP

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07:47 EDT CalAmp's LoJack Mexico signs partnership agreement with Overhaul Group - CalAmp announced its subsidiary, LoJack Mexico, has signed a partnership agreement with Overhaul Group. By integrating Overhaul's real-time supply chain integrity solution with CalAmp's telematics and LoJack Mexico's Stolen Vehicle Recovery services, global enterprises are able to secure shipments of pharmaceuticals, perishables and high-value electronics across Mexico during these uncertain times.
RVMD ALLO

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07:47 EDT Revolution Medicines appoints Eric Shmidt, Peter Svennilson to board - Revolution Medicines (RVMD) announced the appointments of Eric Schmidt, Ph.D., and Peter Svennilson to its board of directors. Mr. Svennilson was appointed to fill the vacancy created by the resignation of Larry Lasky, Ph.D., who stepped down from the board of directors and will continue supporting the company as a scientific advisor. Schmidt currently serves as the chief financial officer of Allogene Therapeutics (ALLO). Svennilson founded The Column Group in 2007 and has worked in venture capital and finance for more than 35 years.
HTBX

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07:46 EDT Heat Biologics initiates first clinical trial site for PTX-35 - Heat Biologics announced initiation of the first clinical trial site for PTX-35. PTX-35 is a novel antibody T-cell co-stimulator targeting TNFRSF25, a receptor that is preferentially expressed by antigen-experienced T cells. TNFRSF25 agonism leads to activation of antigen-experienced memory CD8+ T cells, which are instrumental for tumor destruction. Preclinical studies have demonstrated that PTX-35, in combination with antigen-driven immunotherapies, resulted in enhanced anti-tumor properties, including potent proliferation of antigen-specific T cells, production of effector cytokines and augmented effector immune function. A favorable safety profile was demonstrated in preclinical studies, with no deleterious cytokine release in mice, non-human primates or in vitro human immune cells.
NEPH

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07:45 EDT Nephros to join Russell Microcap Index - Nephros announced that it is set to join the Russell Microcap Index at the conclusion of the 2020 Russell indexes annual reconstitution, effective after the US market opens on June 29, according to a preliminary list of additions posted June 5.
PRIM

Hot Stocks

07:43 EDT Primoris announces solar award valued over $155M - Primoris Services announced a new solar award valued over $155M. The contract was secured by the Power, Industrial, & Engineering segment. The award is for the engineering, procurement, and construction of a utility-scale solar facility in the Southwest. The scope of work includes foundations, electrical, mechanical, and civil construction. Work to support the initial engineering, site investigation, long lead procurement, and cost optimization commenced in the first quarter of 2020, with project completion expected in the fourth quarter of 2021.
BBIO

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07:42 EDT BridgeBio enters collaboration agreement with Johns Hopkins University - BridgeBio Pharma announced that it has entered into a collaboration agreement with Johns Hopkins University to support the translation of academic innovations in genetically driven diseases with a goal of clinical development and potential commercialization to reach patients in need. BridgeBio has a deep interest in understanding where great science is occurring and determining how it can support translating academic findings into treatments for patients, including by helping advance the important discoveries in genetic drivers of specific diseases made at Johns Hopkins. The company is focused on building relationships with academic partners to smooth and speed up the transition from the lab to the patient. BridgeBio will focus on opportunities to support the incredible, early-discovery research around genetically validated targets underway at Johns Hopkins. Where possible, BridgeBio will invest heavily in programs to accelerate promising genetic-disease therapies to the clinic, from gene therapy to small molecule. It will lend its expertise to science designed to help develop a promising molecule or approach into a viable preclinical program, including medicinal chemistry for small-molecule hit optimization, strategies to modify or formulate a potential biologic therapy or approaches for testing non-optimized viral vectors. Additionally, BridgeBio may conduct proof-of-concept studies for lead therapeutic compounds in relevant mammalian models.
BBIO

Hot Stocks

07:41 EDT BridgeBio, University of Florida announce strategic collaboration - BridgeBio Pharma entered into a strategic collaboration with the University of Florida to translate research in genetically driven disease towards clinical development and potential commercialization. The partnership combines University of Florida's prowess in studying genetically driven disease, including its capabilities in gene therapy, with BridgeBio's expertise in efficiently advancing therapeutics from the academic laboratory through preclinical studies and into human testing. BridgeBio believes that, too often, promising research in academia sits on the shelf without partners to move it forward. The company's mission is to bring as much of that research forward as possible, by focusing on establishing partnerships with leading institutions in the hopes of translating research into life-saving therapies. BridgeBio will provide sponsorship to select research programs around diseases with a genetic basis, including gene therapies and large and small molecules. The company will provide guidance for sponsored programs around medicinal chemistry for small-molecule hit optimization, strategies to modify or formulate a potential biologic therapy or approaches for testing non-optimized viral vectors. BridgeBio may conduct proof-of-concept studies for lead therapeutic compounds in relevant mammalian models. BridgeBio seeks to revolutionize partnerships between drug development companies and biomedical research institutions by moving away from one-off interactions and building long-term partnerships based on trust, engagement, science and respect. The company is committed to acting responsibly towards the academic investigators who are on the front lines of understanding the mechanisms of genetically driven diseases and have great insights into how these diseases may be treated.
SNR

Hot Stocks

07:40 EDT New Senior Investment provides update amid COVID-19 pandemic - The company said, "To date, our operators have reported a total of 172 positive cases across 25 properties (119 residents / 53 associates). As of June 16, our operators reported 13 current resident cases across 3 properties, representing less than 0.2% of our current resident population. 76% of the properties in our portfolio have had zero confirmed cases to date. Rate of new cases on a trailing three week average has declined 91% from peak levels in April. Over 1,200 residents and associates have been tested for COVID-19; 86% of those individuals have tested negative. Unclear how the rate of new cases will change as the pandemic continues and restrictions are lifted. Our operators are focused on safely lifting restrictions within our properties in a phased approach. Dependent on local mandates and the absence of any active or suspected COVID-19 positive cases within the community. As of June 16, over 90% of properties have begun lifting restrictions within the property. Over 30% of properties have moved to the second phase of recovery, which allows for expanded dining, activities, visitation and sales functions. Expect ongoing evaluation of the recovery phases as properties continue to lift restrictions. Since our last update (June 2), we have finalized May results and believe it is appropriate to update our view on 2Q20 NOI expectations in light of the actual results for May and the latest trends we are observing for June. 2Q20 results trending better than expected due to: i) less severe occupancy declines as the quarter progressed; ii) lower than expected COVID-19 expenses; and iii) lower than expected variable and fixed costs. As a result, 2Q20 NOI is currently trending closer to down 5% YoY, significantly better than initial estimate provided in May of down 10% to 15% YoY. Ultimate impact of the COVID-19 pandemic will depend on a variety of factors, and it remains too early to estimate the complete effects of the pandemic on the Company's results."
DRNA

Hot Stocks

07:40 EDT Dicerna receives rare pediatric disease designation for nedosiran from FDA - Dicerna Pharmaceuticals announced that the FDA has granted rare pediatric disease designation for nedosiran, an investigational RNAi therapy being developed as a once-monthly treatment for primary hyperoxaluria, or PH. Dicerna said in a release, "PH is a family of ultra-rare, life-threatening genetic disorders that cause complications in the kidneys. There are three known types of PH (PH1, PH2 and PH3), each resulting from a mutation in one of three different genes. Nedosiran is the Company's lead product candidate and is in development for PH types 1, 2 and 3. Under the FDA's rare pediatric disease designation program, the FDA may grant a priority review voucher to a sponsor who receives a product approval for a "rare pediatric disease," which is defined as a serious or life-threatening disease in which the serious or life-threatening manifestations primarily affect individuals aged from birth to 18 years and affects fewer than 200,000 people in the U.S. Subject to FDA approval of nedosiran for the treatment of PH, Dicerna would be eligible to receive a voucher that may be redeemed to receive priority review for a subsequent marketing application for a different product candidate or which could be sold or transferred."
OESX

Hot Stocks

07:39 EDT Orion Energy secures initial $3.1M award for U.S. government retrofit project - Orion Energy Systems announced the receipt of an approximate $3.1M award related to the LED lighting retrofit of a U.S. government facility. Orion will install LED lighting systems in a large government facility in Nevada. The lighting retrofit project is expected to commence in Orion's fiscal 2021 second quarter and be completed during Orion's fiscal 2022. O
BGNE

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07:38 EDT BeiGene announces EMA acceptance of MAA for BRUKINSA - BeiGene announced that its marketing authorization application for BRUKINSA for the treatment of patients with Waldenstrom's macroglobulinemia who have received at least one prior therapy or as first-line treatment for patients unsuitable for chemo-immunotherapy has been validated for regulatory review by the European Medicines Agency. Clinical data in the MAA include the Phase 3 randomized, open-label, multicenter ASPEN clinical trial that evaluated zanubrutinib versus ibrutinib in patients with relapsed/refractory or treatment-naive WM which was recently presented at the 2020 American Society of Clinical Oncology Virtual Scientific Program and the 25th European Hematology Association Congress. The safety package in the MAA included pooled safety data from 779 patients with B-cell malignancies treated with BRUKINSA in six clinical trials.
FRAN

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07:36 EDT Francesca's says cash position increased to $21M as of June 12 - The company said, "As the Company's boutiques began to reopen, its cash position increased to approximately $21.0 million as of June 12, 2020 from $14.3 million as of May 2, 2020. This increase was primarily due to the Company's efforts to drive sales and monetize existing inventory, aggressively reducing costs and managing cash flows, including deferring payments for rent, inventory and other accounts payable, subject to discussions with landlords and vendors. Additionally, the Company also expects to receive an income tax refund of $10.7 million related to certain provisions under the Corona Aid, Relief and Economic Security Act during the second quarter of fiscal year 2020. This refund is required to be used to repay the approximately $5.0 million in outstanding borrowings under the ABL Credit Agreement as of May 2, 2020 along with any other then outstanding borrowings under the ABL Credit Agreement in accordance with the letter agreement entered into between the Company and the ABL Credit Agreement lenders. As of June 12, 2020, the Company had no borrowing base availability under its ABL Credit Agreement."
KR

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07:35 EDT Kroger reports net total debt to adjusted EBITDA ratio 1.81 vs. 2.54 a year ago - The company's net total debt to adjusted EBITDA ratio target range is 2.30-2.50. Kroger held temporary cash investments of approximately $2.3B as of the end of the quarter, reflecting improved operating performance and significant improvement in working capital.
FRAN

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07:34 EDT Francesca's sees 'substantial doubt' over ability to continue as going concern
KR

Hot Stocks

07:33 EDT Kroger reports Q1 gross margin 24.3% - Gross margin was 24.3% of sales for the first quarter. The FIFO gross margin rate excluding fuel increased 44 basis points, due to sales leverage related to shrink, transportation, warehousing and advertising costs.
FRAN

Hot Stocks

07:33 EDT Francesca's delays filing of Quarterly Report on Form 10-Q - The company said, "As a result of the COVID-19 pandemic and as previously disclosed, the Company is delaying the filing of its Quarterly Report on Form 10-Q for the thirteen weeks ended May 2, 2020 as it needs more time to finalize its asset impairment assessments, including the related income tax effect. The Company expects to file its Form 10-Q within 45 days from June 16, 2020."
KR

Hot Stocks

07:33 EDT Kroger reports Q1 identical sales, without fuel, up 19% - Reports Q1 digital sales up 92%.
CARS

Hot Stocks

07:33 EDT Cars.com appoints Sonia Jain as CFO - Cars.com has concluded its search for CFO and has appointed Sonia Jain to the role effective July 6. Jain joins Cars.com from Redbox where she served as CFO. Prior to Redbox, Sonia served as VP, finance and treasurer with Outerwall. Jandy Tomy has served as interim CFO of CARS since January 2020. Jandy will resume her treasurer position as well as other finance responsibilities for the company consistent with her personal objectives.
FRAN

Hot Stocks

07:32 EDT Francesca's reports 593 boutiques reopened as of June 23 - The company said, "The COVID-19 pandemic resulted in the temporary closure of all of the Company's 703 boutiques beginning on March 25, 2020. On April 30, 2020, the Company began to reopen its boutiques in locations where local shutdown orders have been lifted. As of June 12, 2020, a total of 593 boutiques have reopened although the majority of them are operating at reduced capacity and hours in accordance with local regulations. In conjunction with such boutique reopenings, more than half of all furloughed corporate and boutique employees have been recalled. The Company plans to continue to reopen boutiques and recall furloughed employees as local mandates are lifted. All boutiques will strictly adhere to then current Center for Disease Control and Prevention recommendations and local regulations to protect the health and safety of its sales associates and customers. Additionally, as of June 12, 2020, there continues to be an overall disruption in the Company's supply chain and operations and the Company's ecommerce and distribution facility remain to be operating at reduced capacity. As a result of the COVID-19 pandemic, the Company's revenues, results of operations and cash flows continue to be materially adversely impacted which continues to raise substantial doubt about its ability to continue as a going concern. Management continues to take aggressive and prudent actions to reduce expenses to preserve cash on hand."
KR

Hot Stocks

07:32 EDT Kroger 'not reaffirming or providing new 2020 guidance' - The company said, "The COVID-19 pandemic has dramatically changed the outlook for food retail in 2020 and we continue to monitor, evaluate and adjust our plans to address the impact to our business. There are still many unknown factors related to the long-term impact of COVID-19 that could influence our financial results for the remainder of 2020, such as: continued investments to help our customers and associates, uncertainty surrounding consumer behavior, restrictions and what will be the new normal, and potential long-term shift in customers eating more food at home. In recognition of these factors, it is difficult to predict specific outcomes and as such Kroger is not reaffirming or providing new 2020 guidance. While we expect to exceed the outlook shared in our April 1 business update for identical sales without fuel, adjusted FIFO operating profit, adjusted EPS and adjusted free cash flow, the company is not able to forecast the extent of such upside for the reasons mentioned above. Kroger's financial model has proven to be resilient throughout the economic cycle. We remain confident in our business model as well as our ability to generate strong free cash flow and achieve sustainable and attractive total shareholder returns."
FRAN

Hot Stocks

07:31 EDT Francesca's CEO says 'optimistic about our future' - Francesca's Holdings Corporationprovides an update on its COVID-19 response and reports select preliminary financial results for the first quarter ended May 2, 2020. These preliminary results do not include the impact of non-cash impairment charges of long-lived assets, including the related income tax effect, which are expected to have a material impact on the Company's reported results. Andrew Clarke, President and CEO, stated, "While we continue to navigate through this difficult period, we are highly encouraged to see bright spots in our business driven by the new strategies that we have been testing and scaling. We are very pleased with the continued strong momentum in our ecommerce business and heartened by the sales results in the boutiques we have reopened. Since the outbreak of COVID-19, we have taken measures to improve liquidity by driving sales and monetizing existing inventory, aggressively reducing costs, and managing cash flows, which, together with deferring rent and vendor payments, enabled us to increase our cash position to approximately $21M as of June 12, 2020. I want to thank the entire team for their tremendous commitment and hard work towards these efforts. Looking ahead, we are optimistic about our future as we execute our differentiated business model. Our boutiques provide a broad end-use assortment that is curated and merchandised for outfitting while at the same time offer a treasure hunt experience to our customers. As we begin crafting the future for francesca's, there is also a focus on enhancing our omni channel capabilities, specifically through re-platforming our e-commerce site to support greater scale. As we combine our customer centric approach with omni channel capabilities we see tremendous opportunity to gain market share and get us back on track to deliver profitable growth."
LTRX

Hot Stocks

07:16 EDT Lantronix appoints Robert Adams as head of corporate development, IR - Lantronix announced that Robert Adams has joined Lantronix as Head of Corporate Development and Investor Relations. Prior to joining Lantronix, Adams was senior vice president of Corporate Development for Microsemi Corp.
IAG

Hot Stocks

07:15 EDT IAMGold intersects 10.5m at 10.5 g/t AU at Nelligan project - Vanstar Mining Resources announced initial assay results from its 2020 exploration diamond drilling program completed at its Nelligan joint venture project, IAMGOLD Corporation: 75%, Vanstar: 25%, located 60 kilometres southwest of Chibougamau, Quebec, Canada. The Company is reporting assay results from six diamond drill holes totaling 3,717 metres completed as part of the 2020 drilling program. Assays are pending from a further three completed drill holes totaling 1,278 metres. The Nelligan Gold project hosts Inferred Mineral Resources containing 3.2 million ounces of gold grading 1.02 g/t Au. The 2020 diamond drilling program was designed to infill selected areas of the resource to upgrade resource classification from Inferred to an Indicated category and evaluate potential resource extensions at depth and along strike. In response to the global COVID-19 crisis, IAMGOLD temporarily suspended its diamond drilling program in progress on the Nelligan project on March 23rd. The 2020 exploration drilling program was planned to involve the completion of approximately 8,000 metres focused on infill drilling to improve resource classification as well as step-out drilling to evaluate potential resource extensions at depth and along strike. A total of 4,995 metres of diamond drilling were completed up to the suspension of the program. A summer drilling campaign is currently being designed to complete the drilling program, taking into consideration summer access conditions as well as the implementation of safety protocols to prevent COVID-19 infections. All pending assay results from drilling completed to date will be reported once they are received, validated and compiled. Additional metallurgical tests are also planned in the coming months to provide additional information on the metallurgical recoveries from the various zones of mineralization comprising the Mineral Resources of the Nelligan gold deposit and to further refine the process flow sheet parameters. The geological, geochemical and structural models have been updated and refined to assist the selection of representative metallurgical samples and to support further deposit studies. Regional exploration activities will also continue to define and evaluate other priority targets on the property with focused geological mapping programs supported by geochemical and geophysical surveys as merited.
LEE

Hot Stocks

07:10 EDT Lee Enterprises expects to achieve $100M in cost synergies by end of FY21 - Tim Millage, VP, CFO and Treasurer, said, "As we focus on driving top-line growth across our markets, we remain vigilant on costs. As we evaluate the post-pandemic operating environment and integration of BHMG and Buffalo, we expect to realize more than $100M of cost synergies by the end of fiscal year 2021. The comprehensive refinancing closed in March solves our looming maturities, and provides several important benefits.We lowered our cost of capital at a fixed rate and have no fixed mandatory principal payments. Further, the lack of financial performance covenants and a 25-year maturity provide a runway to drive shareholder value over the long term. We are thrilled to have completed our financing at highly attractive terms, and to strengthen our relationship with Berkshire Hathaway."
WFC

Hot Stocks

07:09 EDT Wells Fargo to sell GAI feeder fund platform to iCapital Network - Wells Fargo announced that Wells Fargo Investment Institute, or WFII, has entered into an agreement to sell its global alternative investments, or GAI, feeder fund platform to iCapital Network. In addition, Wells Fargo announced that it is making a strategic investment in iCapital under the terms of iCapital's latest fundraising round. The Wells Fargo GAI feeder fund platform provides brokerage and wealth management clients the ability to invest in a full suite of alternative solutions, including private equity, private debt, hedge funds, private real estate and direct private investments across approximately 70 investment vehicles. Since 2006, GAI has offered investment options through feeder funds that invest in external funds or portfolio companies. As part of the transaction, iCapital will offer employment to a team of Wells Fargo employees who currently support operations for the GAI feeder fund platform. The transaction is subject to customary closing conditions and is expected to close during the second half of 2020. Terms of the agreement were not disclosed.
TNXP

Hot Stocks

07:05 EDT Tonix Pharmaceuticals, Southern Research expand COVID-19 vaccine collaboration - Tonix Pharmaceuticals Holding announced an expansion of its strategic collaboration with Southern Research to include a study of T cell immune responses to SARS-CoV-2 in volunteers who have recovered or remain asymptomatic after exposure to COVID-19. The research is part of an ongoing and broader collaboration between Tonix and Southern Research to develop and conduct animal testing of Tonix's TNX-1800, which is a live replicating virus vaccine designed to protect against COVID-19. The data will support the interpretation of animal trial results with TNX-1800, which are expected in the fourth quarter of 2020 and subsequent human trials. A team of scientists from Southern Research, including Raj Kalkeri, Ph.D., Elizabeth Wonderlich, Ph.D., John Farmer, Ph.D. and Fusataka Koide, Director of Virology, is working on this collaboration.
SLDB VRTX

Hot Stocks

07:04 EDT Solid Biosciences appoints Ian Smith as chairman of board - Solid Biosciences (SLDB) announced the appointment of board member Ian Smith as chairman of the board. Smith succeeds Andrey Zarur, Ph.D., who served as chairman of the board since 2013 and is one of the co-founders of Solid Biosciences. The appointment is effective June 16, 2020. Smith most recently serving as EVP and COO of Vertex Pharmaceuticals (VRTX).
CDNA

Hot Stocks

07:02 EDT CareDx announces FDA acceptance of LOI for iBox Scoring System - The company said, "CareDx congratulates the Critical Path Institute's Transplant Therapeutics Consortium on the U.S. Food and Drug Administration accepting the iBox Scoring System into the Center for Drug Evaluation and Research's Biomarker Qualification Program. TTC provided information supporting the qualification of the iBox Scoring System as a reasonably likely surrogate endpoint for clinical trials evaluating immunosuppressive therapies for use in kidney transplant recipients, allowing drug sponsors to purse accelerated approval. FDA indicated in its decision that it supports TTC's intent to pursue biomarker qualification for the iBox Scoring System and invited TTC to submit a Qualification Plan. CareDx currently offers KidneyCare, which is a prediction tool based on iBox technology, alongside AlloSure and AlloMap, for informing the clinical care and management of transplant patients."
SMTS

Hot Stocks

07:01 EDT Sierra Metals confirms new high-grade zone at Cusi Mine, Mexico - Sierra Metals announced the discovery of a new high-grade silver zone with significant widths in an area called Northeast-Southwest System of Epithermal Veins at its Cusi Mine in Mexico. The new high-grade silver vein system was discovered through confirmatory drilling which includes true widths of 17.45 meters of 428 g/t silver - 464 g/t silver equivalent -, 9.35 meters of 304 g/t silver - 327 g/t silver equivalent -, 8.75 meters of 303 g/t silver - 322 g/t silver equivalent - and 4.90 meters of 1,140 g/t silver - 1,163 g/t silver equivalent-. The new discovery is an extension of the Cusi Vein systems in the North East of the fault and, rather than barren, the veins are reporting silver grades and widths above the average of the structures previously known at the mine in the South West to the Cusi fault. The company has plans to drill an additional 1,000 meters to better understand the extension. The Cusi Mine remained in care and maintenance during the government-mandated shutdowns. Cusi production is expected to recommence after the mine development work is completed and once a process can be implemented at the mine to mitigate risk to employees at the site. Management is targeting a ramp-up to 1,200 tons per day by the end of the year, at which point the Cusi mine is expected to become self-sustainable and cash flow positive. Additionally, during the second half of the year, studies will commence on the potential expansion of Cusi. Management also believes there is further brownfield potential in areas not previously explored but which are very close to the Santa Rosa de Lima zone.
CMC

Hot Stocks

07:00 EDT Commercial Metals sees construction, infrastructure activity remaining resilient - "We expect construction and infrastructure activity to remain resilient during our fiscal fourth quarter," said CEO Barbara Smith. "Our finished product volumes are supported by strong fabrication backlogs, which stood near record-high levels at May 31. Customers' sentiment about their own summer construction workloads is also encouraging. CMC's net debt-to-EBITDA ratio of 1.2x and substantial cash and equivalents on hand give us great confidence in our ability to withstand these challenging times, and provide us with significant flexibility in our capital allocation decisions."
DBI

Hot Stocks

06:53 EDT Designer Brands has reopened 90% of total store base - The Company has reopened approximately 90% of its total store base. The company expects to have nearly all North American stores open by the end of June. The company has implemented a number of measures to protect the health and safety of its customers and associates as stores are reopened.
KKR

Hot Stocks

06:51 EDT KKR announces Q2 monetization activity update - KKR announced a monetization activity update for the period from April 1 through June 17. Based on information available to us as of today, with respect to the period through June 17, KKR has earned gross realized carried interest and total realized investment income of approximately $400M. This is driven primarily by strategic and secondary sale transactions that have closed quarter to-date, as well as dividend and interest income from KKR's balance sheet portfolio. The estimate disclosed above is not intended to predict or represent the total revenues for the full quarter ending June 30, because it does not include the results or impact of any other sources of income, including fee income, or expenses. This estimate is also not necessarily indicative of the results that may be expected for any other period, including the entire year ending December 31, 2020.
APO...

Hot Stocks

06:49 EDT Apollo Global expanding insurance asset management business - Apollo Global (APO) is expanding its insurance asset management business, as Athene Holding (ATH) has entered into a fixed annuity block reinsurance transaction with Jackson National Life Insurance, a subsidiary of Prudential (PRU), with the support of Athene Co-Invest Reinsurance Affiliate. Athene will reinsure a $27B in-force block of fixed deferred and fixed indexed annuities. Athene will also make a $500M equity investment in Jackson, representing an 11% stake in the company. Apollo's insurance platform is anchored by permanent capital vehicle assets from Athene and other insurance platforms. Through Q1 and pro forma for Athene's transaction with Jackson, additional transactions and internal growth, Apollo has added nearly $80B in insurance-related assets under management. Apollo expects this transaction will be immediately accretive; however, the full financial effect is expected to be achieved on a run rate basis in the second half of 2021.
EBS

Hot Stocks

06:33 EDT Emergent BioSolutions investing $75M in Canton site expansion - Emergent BioSolutions will expand its contract development and manufacturing capabilities by expanding into viral vector and gene therapy. The company will invest $75M in its Canton, Massachusetts facility, which is focused on the development and manufacturing of drug substance for live viral vaccines, including the company's smallpox vaccine. The company plans to provide full molecule-to-market CDMO services for viral vector and gene therapy innovators, by offering development services out of its Gaithersburg location, drug substance manufacturing out of Canton, and drug product manufacturing at its Rockville location, which is in the midst of an expansion that is scheduled to be operational at the end of 2021.
GOOG...

Hot Stocks

06:19 EDT Google's purchase of Fitbit raises preliminary competition concerns, says ACCC - The Australian Competition and Consumer Commission outlined preliminary concerns with Google's (GOOGL) proposed acquisition of Fitbit (FIT), stating that Google's access to consumer health data may raise entry barriers, further entrench its dominant position and adversely affect competition in several digital advertising and health markets. "Our concerns are that Google buying Fitbit will allow Google to build an even more comprehensive set of user data, further cementing its position and raising barriers to entry to potential rivals," ACCC Chair Rod Sims said. "The ACCC's Digital Platforms Inquiry found that Google's substantial market power is built on its concentration of search and location data, and data collected via third-party websites and apps."
MTDR

Hot Stocks

06:14 EDT Matador reports initial Ray State well results, provides operational update - Matador Resources announced results from the first five wells completed and turned to sales on the Ray State tract in the Rustler Breaks asset area and provided updates on the Rodney Robinson wells in the Antelope Ridge asset area and upcoming milestones for the remainder of 2020. The five Ray State wells in the eastern portion of the Rustler Breaks asset area were completed and turned to sales in May and early June with 24-hour initial potential aggregate test results of approximately 12,500 BOE/day, including 7,600 barrels of oil per day and 29.5 MMcf natural gas per day. The six Rodney Robinson wells recently completed and turned to sales in the western portion of the Antelope Ridge asset area should produce, in aggregate, over 1M BOE, including approximately 750K Bbl of oil, before the end of Q2. Matador is concluding completion operations on its five Leatherneck wells in the southern portion of the Arrowhead asset area and has also initiated completion operations on the initial 13 Boros wells drilled in the Stateline asset area. The Leatherneck wells should be turned to sales in August, with the Boros wells being turned to sales beginning in September. In Q3, San Mateo Midstream II, is expected to complete and place in service its main midstream project for the year, a gas processing expansion of its present Black River plant. At that point in time, San Mateo, the company's 51% owned midstream joint venture expects to finish its 200 Mmcf per day expansion of the Black River cryogenic natural gas processing plant and to extend San Mateo's total processing capacity to 460 MMcf of natural gas per day. This expansion project continues to be on time and on budget. Beginning in September 2020, the fourth and most significant production milestone should be reached, when Matador anticipates it will begin production from the first 13 wells being drilled in the eastern portion of the Stateline asset area. Matador has a 100% working interest and an 87.5% net revenue interest in each of these wells.
BGG

Hot Stocks

06:14 EDT S&P downgrades Briggs & Stratton to SD, unlikely to make interest payment - S&P Global Ratings on Wednesday downgraded its issuer credit rating on Briggs & Stratton to 'SD' from 'CCC-' because it believes the company is unlikely to make the interest payment on the notes within the 30-day grace period but expect that it will continue to pay interest on its asset-based lending revolving credit facility. S&P also lowered its issue-level rating on the company's unsecured notes to 'D'.
CCL

Hot Stocks

06:14 EDT Carnival down 3.5% after reporting Q2 results
CCL

Hot Stocks

06:13 EDT Carnival estimates ongoing ship operating, administrative expenses $250M/month - Carnival said in its Q2 earnings release, "The company estimates that its ongoing ship operating and administrative expenses will be approximately $250 million per month once all ships are in paused status. The company continues to seek ways to further reduce this monthly requirement. The company has taken significant actions to reduce operating expenses during the pause in guest operations: While maintaining safety, environmental protection and compliance, the company significantly reduced ship operating expenses, including crew payroll, food, fuel, insurance and port charges by transitioning ships into paused status, either at anchor or in port and staffed at a safe manning level; Currently 62 of the company's ships are in their final expected pause location. The company expects substantially all of its ships to reach their full pause status during the third quarter; Significantly reduced marketing and selling expenses; Implemented a combination of layoffs, furloughs, reduced work weeks and salary and benefit reductions across the company, including senior management; Instituted a hiring freeze across the organization, significantly reduced consultant and contractor roles. The company has reduced capital expenditures and estimates $300 million of non-newbuild capital expenditures during the second half of 2020, which largely consists of previously committed expenditures. The company previously had four ships scheduled to be delivered between May and October of 2020. The company believes COVID-19 has impacted shipyard operations and will result in delivery delays of the ships this year and is working with the shipyards on revised timing. The company has committed future financing, comprised of ship export credit facilities, associated with these newbuilds."
MAC

Hot Stocks

06:12 EDT Macerich reopens most retail properties, shopping centers - Macerich announced that all 47 of the company's retail properties nationwide are now open for business. All Macerich shopping centers are welcoming shoppers, with the exception of six properties in New York, two in New Jersey and one in Pennsylvania. Those properties currently offer limited retail operations, included as permitted based on state regulations "curbside pickup" and retail with exterior access. Significantly, several centers are demonstrating a "strong" return to business, with traffic numbers approaching near normal levels. For example, South Plains Mall in Texas, one of the earliest Macerich centers to open on May 1, experienced 93.5% of year-over-year traffic on June 14. Similarly, Vintage Faire Mall in California's Central Valley reported 97.1 % of year-over-year traffic on the same day, after being fully open since May 22. In Colorado, FlatIron Crossing, which just reopened on June 16, reported initial traffic of 33% on its first day, with evidence of sizable shopper intent; many stores reported higher-than-expected conversion rates. Macerich now has new protocols in place to meet needs, including enhanced cleaning and sanitizing, social distance queuing, path of travel, security, deliveries, furniture placement and more, all developed per industry best practices and CDC recommendations.
CCL

Hot Stocks

06:10 EDT Carnival reports $2.6B in deposits as of May 31 - Carnival said in its Q2 earnings release, "The company's brands have announced various incentives and flexibility for certain booking payments on select sailings to support guest confidence in making new bookings. These incentives vary by brand and sailing and include onboard credits and reduced or refundable deposits. In addition, the company is providing flexibility to guests with bookings on sailings cancelled due to the pause by allowing guests to receive enhanced future cruise credits, or FCC, or elect to receive refunds in cash. Enhanced FCCs increase the value of the guest's original booking or provide incremental onboard credits. As of May 31, approximately half of guests affected have requested cash refunds. Despite substantially reduced marketing and selling spend, the company is seeing growing demand from new bookings for 2021. For the six weeks ending May 31, approximately two-thirds of 2021 bookings were new bookings. The remaining 2021 booking volumes resulted from guests applying their FCCs to specific future cruises. As of May 31, the current portion of customer deposits was $2.6 billion with $121 million relating to third quarter sailings and $353 million relating to fourth quarter sailings. The company expects any decline in the customer deposits balance in the second half of 2020, all of which is expected to occur in the third quarter, to be significantly less than the decline in the second quarter of 2020. As of May 31, cumulative advanced bookings for the full year of 2021 capacity currently available for sale are within historical ranges at prices that are down in the low to mid-single digits range including the negative yield impact of FCCs and onboard credits applied, on a comparable basis. For the full year of 2021, booking volumes for the six weeks ending May 31, were running meaningfully behind the prior year. However, the company saw an improvement in booking volumes for the six weeks ending May 31, compared to the prior six weeks."
MGM

Hot Stocks

06:07 EDT MGM Resorts JV to be sports betting partner of Confederate Tribes of Grand Ronde - Roar Digital, the joint venture, or JV, between MGM Resorts and GVC Holdings, and the Confederate Tribes of Grand Ronde announced a long-term partnership. Roar Digital will be the Tribes' exclusive sports betting partner. Roar Digital will open a BetMGM sportsbook at Spirit Mountain Casino this year. Spirit Mountain Casino is the largest casino in Oregon. Along with retail sports betting, Roar Digital will roll out an on-reservation mobile sports betting app, as well as an eventual state-wide online sports betting offering, as it becomes available to the Tribe, pending regulatory approval.
CCL

Hot Stocks

06:07 EDT Carnival expects to resume guest operations 'in phased manner' - Carnival said in its Q2 earnings release "The company expects to resume guest operations, after collaboration with both government and health authorities, in a phased manner, with specific ships and brands returning to service over time to provide its guests with enjoyable vacation experiences. The company anticipates that initial sailings will be from a select number of easily accessible homeports. The company expects future capacity to be moderated by the phased re-entry of its ships, the removal of capacity from its fleet and delays in new ship deliveries. In connection with its capacity optimization strategy, the company intends to accelerate the removal of ships in fiscal 2020 which were previously expected to be sold over the ensuing years. The company already has preliminary agreements for the disposal of 6 ships which are expected to leave the fleet in the next 90 days and is currently working toward additional agreements. In preparation for the resumption of its cruises, and consistent with its commitment to provide its guests with a safe and healthy environment, the company is proactively consulting and working in close cooperation with various medical policy experts and public health authorities to develop enhanced procedures and protocols for health and safety onboard its ships. The company appreciates the excellent working relationship with the health authorities of federal states and local port authorities in Germany, as well as the Italian Coast Guard, Italian Ministry of Transportation, Italian Ministry of Health and others around the world. A comprehensive restart protocol may include areas such as medical care, screening, testing, mitigation and sanitization addressing arrival and departure at cruise terminals, the boarding and disembarkation process, onboard experiences and shore excursions."
DISH TMUS

Hot Stocks

06:04 EDT Dish confirms it will acquire Boost from T-Mobile by July 1 - In a regulatory filing on Wednesday, Dish (DISH) confirmed that it and T-Mobile (TMUS) entered into a first amendment to the asset purchase agreement under which the parties agreed to: (i) close the Boost transaction in accordance with the APA on July 1, 2020; and (ii) therefore, extend the termination date of the APA to July 1, 2020, such that neither DISH nor T-Mobile can terminate the APA due to the occurrence of the termination date prior to July 2, 2020, in each case subject to the terms and conditions of the APA and the DOJ Final Judgment.
FAMI

Hot Stocks

06:03 EDT Farmmi subsidiary receives repeat order for Shiitake mushrooms in Israel - Farmmi announced its subsidiary, Zhejiang Forest Food, has received an additional repeat order for distribution of its Shiitake mushrooms and black fungus in Israel.
RUBI

Hot Stocks

06:01 EDT Rubicon Project COO Mark Zagorski to resign at end of June - Rubicon Project announced that Mark Zagorski, President and COO, will resign at the end of June to pursue a new opportunity. Michael Barrett will re-assume the President role with general responsibility for the management and control of the operations of the corporation.
KKR

Hot Stocks

06:01 EDT KKR to acquire Roompot Group from PAI Partners, terms not disclosed - KKR announces an agreement to acquire Roompot Group from European private equity firm PAI Partners. KKR said in a release, "The transaction is subject to customary closing conditions, having already received positive works council advice. Financial terms are not disclosed. Under PAI's ownership, Roompot has invested significantly in upgrading and expanding its accommodations and opening new parks, developed a strong digital marketing and distribution platform, increased real estate ownership and grown revenue and EBITDA at double digit growth rates. The company now welcomes three million guests and 13 million overnight stays each year, generating revenues of almost EUR 400 million."
ATH PUK

Hot Stocks

05:41 EDT Athene announces fixed annuity reinsurance transaction with Jackson National - Athene Holding (ATH) has announced a fixed annuity block reinsurance transaction with Jackson National Life and subsidiary of Prudential (PUK), with the support of Athene Co-Invest Reinsurance Affiliate, or ACRA. Athene said in a release, "Under the terms of the agreement, Athene will reinsure a $27B in-force block of fixed deferred and fixed indexed annuities. As part of the transaction, Athene is making a $500M equity investment in Jackson, representing an 11% stake in the company, which will help Jackson to pursue various growth initiatives aligned with its commercial diversification strategy. The transaction is expected to be accretive to Athene's adjusted operating income in 2021 and 2022, with potential upside as portfolio redeployment occurs. Athene expects to deploy approximately $1.2 billion of total capital in connection with the transaction to be contributed over the next 12-18 months, including a further investment of capital in connection with portfolio redeployment, as well as the equity investment in Jackson. Utilizing the strategic benefits of ACRA, 63% of the total capital deployment will be funded by third-party investors, and 37% will be funded by Athene on a standalone basis. Pro forma for the transaction, as well as the company's recent Series C preferred stock offering, Athene continues to have significant financial flexibility and a strong capital position, with excess equity capital of $3 billion and total deployable capital of $7.1 billion. Jackson will continue to service and administer the in-force policies within the block. The reinsurance agreement has an effective date of June 1, 2020. The equity investment in Jackson is expected to close in July 2020, subject to customary closing conditions and approvals. Credit Suisse is serving as financial advisor and Sidley Austin LLP is serving as legal counsel to Athene in connection with this transaction."
ATH

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05:38 EDT Athene announces fixed annuity reinsurance transaction with Jackson National - Athene Holding (ATH) has announced a fixed annuity block reinsurance transaction with Jackson National Life and subsidiary of Prudential (PRU), with the support of Athene Co-Invest Reinsurance Affiliate, or ACRA. Athene said in a release, "Under the terms of the agreement, Athene will reinsure a $27B in-force block of fixed deferred and fixed indexed annuities. As part of the transaction, Athene is making a $500M equity investment in Jackson, representing an 11% stake in the company, which will help Jackson to pursue various growth initiatives aligned with its commercial diversification strategy. The transaction is expected to be accretive to Athene's adjusted operating income in 2021 and 2022, with potential upside as portfolio redeployment occurs. Athene expects to deploy approximately $1.2 billion of total capital in connection with the transaction to be contributed over the next 12-18 months, including a further investment of capital in connection with portfolio redeployment, as well as the equity investment in Jackson. Utilizing the strategic benefits of ACRA, 63% of the total capital deployment will be funded by third-party investors, and 37% will be funded by Athene on a standalone basis. Pro forma for the transaction, as well as the company's recent Series C preferred stock offering, Athene continues to have significant financial flexibility and a strong capital position, with excess equity capital of $3 billion and total deployable capital of $7.1 billion. Jackson will continue to service and administer the in-force policies within the block. The reinsurance agreement has an effective date of June 1, 2020. The equity investment in Jackson is expected to close in July 2020, subject to customary closing conditions and approvals. Credit Suisse is serving as financial advisor and Sidley Austin LLP is serving as legal counsel to Athene in connection with this transaction."
HCM

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05:30 EDT Chi-Med granted FDA Fast Track Designation for fruquintinib - Hutchison China MediTech announces that the FDA has granted Fast Track Designation for the development of fruquintinib, for the treatment of patients with metastatic colorectal cancer, or mCRC, who have been previously treated with fluoropyrimidine-, oxaliplatin-, and irinotecan-based chemotherapy, an anti-vascular endothelial growth factor, or VEGF, biological therapy, and, if RAS wild-type, an anti-epidermal growth factor receptor, or EGFR, therapy. Chi-Med is initiating a Phase III registration study, known as the FRESCO-2 study, in refractory mCRC in the U.S., Europe and Japan. FRESCO-2 is expected to start enrolling patients in mid-2020. The U.S. FDA acknowledged that the totality of the fruquintinib clinical data, including the FRESCO-2 study, if positive; the prior positive Phase III FRESCO study demonstrating improvement in overall survival that led to fruquintinib approval for mCRC in China in 2018; and additional completed and ongoing supporting studies in mCRC; could support a New Drug Application for the treatment of patients with mCRC in the third-line setting. The adequacy of the data to support a specific indication will be assessed during the review of a New Drug Application.
BLDP

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05:23 EDT Ballard Power receives follow-on order for 15 fuel cell modules from Wrightbus - Ballard Power Systems announced that it has received follow-on purchase orders for 15 of its 85-kilowatt heavy-duty FCveloCity-HD fuel cell modules from Wrightbus to power Fuel Cell Electric Buses, or FCEBs, planned for deployment in the U.K. Wrightbus was recently re-capitalized by Bamford Bus, after having gone into administration last year. The company said in a release, "Including the 15 modules announced today, Ballard currently has orders in-hand from Wrightbus for a total of 50 modules to power FCEBs in the U.K., 35 of which were previously announced in 2019. Of those 35 modules, 20 are to power buses planned for deployment in London and 15 are for buses planned for deployment in Aberdeen. Ballard expects to ship all 50 modules in 2020."
RHHBY

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05:17 EDT Genentech says Phase III IMpassion031 study met primary endpoint - Genentech announced that the Phase III IMpassion031 study, evaluating Tecentriq in combination with chemotherapy in comparison to placebo plus chemotherapy, met its primary endpoint by demonstrating a statistically significant and clinically meaningful improvement in pathological complete response, or pCR, for the treatment of people with early triple-negative breast cancer, or TNBC, regardless of PD-L1 expression. Genentech said in a release, "In the study, fewer patients who received the Tecentriq combination as a neoadjuvant treatment had evidence of tumor tissue detectable at the time of surgery, regardless of PD-L1 expression, in comparison to the control arm. Neoadjuvant treatment may allow a doctor to quickly assess whether a medicine is working, and may also reduce a tumor's size so it is easier to surgically remove. pCR is a common measure of neoadjuvant treatment effect in breast cancer and can be assessed more quickly than traditional endpoints in early-stage breast cancer. Safety for the Tecentriq combination appeared to be consistent with the known safety profiles of the individual medicines and no new safety signals were identified. Results of the IMpassion031 study will be presented at an upcoming medical meeting and will be discussed with global health authorities including the FDA and European Medicines Agency. Genentech has an extensive development program for Tecentriq, including multiple ongoing and planned Phase III studies across lung, genitourinary, skin, breast, gastrointestinal, gynecological, and head and neck cancers. This includes studies evaluating Tecentriq both alone and in combination with other medicines."
REXN

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05:12 EDT Rexahn Pharmaceuticals, Ocuphire Pharma announce merger agreement - Rexahn Pharmaceuticals and Ocuphire Pharma announced the companies have entered into a definitive merger agreement under which Ocuphire will merge with a wholly-owned subsidiary of Rexahn in an all-stock transaction. The companies said in a release, "Following closing, which is expected to occur in the second half of 2020, the combined company will change its name to Ocuphire Pharma, Inc. and is expected to trade on the Nasdaq Capital Market under the ticker symbol 'OCUP.' The combined company will focus on the advancement of its pipeline of ophthalmic drug candidates. Certain institutional healthcare and other accredited investors, including certain Ocuphire directors and executives, have also committed to invest $21.15 million in a private placement that will close immediately prior to the closing of the merger, assuming the satisfaction or waiver of customary closing conditions. Investors in this pre-merger financing will receive Ocuphire common stock prior to closing, which will convert into Rexahn common stock upon closing of the merger. Additionally, following the closing of the merger, Rexahn will issue to these investors warrants to purchase shares of Rexahn common stock and, potentially, additional shares of Rexahn common stock. Under the terms of the merger agreement, subject to the satisfaction or waiver of customary closing conditions, including (i) the receipt of the required approval of the Ocuphire stockholders and Rexahn stockholders, (ii) the closing of the pre-merger financing and (iii) Rexahn having a minimum amount of net cash at closing, Ocuphire will merge with a wholly-owned subsidiary of Rexahn, with Ocuphire surviving the merger as a wholly-owned subsidiary of Rexahn. Upon completion of the merger, Ocuphire stockholders will receive newly issued shares of Rexahn common stock pursuant to an exchange ratio formula set forth in the merger agreement. Under the terms of the merger agreement, immediately following the consummation of the merger, Rexahn's then-current stockholders would own approximately 14.3% of the combined company's common stock, and the former Ocuphire securityholders would own approximately 85.7% of the combined company's common stock, in each case calculated on a fully-diluted basis, assuming Rexahn's net cash balance at closing is between $3.2 million and $6.0 million. The exchange ratio formula in the merger agreement is subject to adjustment for every $100,000 that Rexahn's actual net cash balance at closing is less than $3.2 million or more than $6 million. Based on Rexahn's current estimates, Rexahn believes that it is reasonably likely to deliver significantly less than $3.2 million at closing."
PTGX

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05:00 EDT Protagonist Therapeutics receives Orphan Drug Designation for PTG-300 - Protagonist Therapeutics announced that the FDA has granted Orphan Drug Designation for PTG-300 for the treatment of polycythemia vera. PTG-300 is an injectable synthetic peptide mimetic of the natural hormone hepcidin currently in clinical development for the treatment of polycythemia vera and hereditary hemochromatosis. "Receiving FDA orphan drug designation is another important milestone for Protagonist and underscores the importance of our work in polycythemia vera," commented Samuel Saks, M.D., Protagonist Chief Medical Officer. "Individuals living with polycythemia vera face a high disease burden. PTG-300 has a non-cytoreductive therapeutic mechanism in the treatment of polycythemia vera and has shown a well-tolerated safety profile to date. Because of its properties, PTG-300 may help provide sustained control of hematocrit and potentially help address symptoms of polycythemia vera and systemic iron deficiency in these patients." Protagonist recently announced initial Phase 2 results in patients with polycythemia vera that demonstrated robust clinical response and clinically meaningful dose related control of hematocrit levels on individual patient basis.