Stockwinners Market Radar for April 12, 2020 - Earnings, Upgrades downgrades, option trades, Best Stock Advisory Service

BP...

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19:59 EDT Fly Intel: Top five weekend stock stories - Catch up on the weekend's top five stories with this list compiled by The Fly: 1. The world's top oil producers pulled off a historic deal to cut global petroleum output by nearly a 10th, putting an end to the devastating price war between Saudi Arabia and Russia, Bloomberg's Javier Blas, Salma El Wardany and Grant Smith reported. OPEC+ will cut 9.7M barrels a day -- just below the initial proposal of 10M, the authors noted. The U.S., Brazil and Canada will contribute another 3.7M barrels on paper as their production declines. Meanwhile, the Saudi energy minister told Reuters on Sunday that effective oil supply cuts by OPEC and its allies will amount to 12.5M barrels per day, because of higher output in April from Saudi Arabia, the United Arab Emirates and Kuwait. Commenting on the agreement, President Donald Trump praised the deal, saying it would save jobs in the U.S. energy industry. Publicly traded companies in the space include BP (BP), Chevron (CVX), ConocoPhillips (COP), Exxon Mobil (XOM), Royal Dutch Shell (RDS.A) and Total (TOT). 2. Gilead (GILD) announced results from a cohort analysis of 53 patients hospitalized with severe complications of COVID-19 who were treated with the investigational antiviral remdesivir on an individual compassionate use basis. The majority of patients in this international cohort demonstrated clinical improvement and no new safety signals were identified with remdesivir treatment, the company said. 64% of the patients in this cohort were on mechanical ventilation at baseline, including four patients also on extracorporeal membrane oxygenation. Treatment with remdesivir resulted in an improvement in oxygen support class for 68% of patients over a median follow-up of 18 days from the first dose of remdesivir. More than half of patients on mechanical ventilation were extubated and nearly half of all patients were discharged from the hospital following treatment with remdesivir. 3. Investors are hoping that a potential peak in the pandemic's death rate means this nightmare may be coming to an end and when this happens, Facebook (FB) will probably prosper, much as it has during this crisis, Steven Sears wrote in this week's edition of Barron's. Many people have been using Facebook to communicate with friends and family during weeks of isolation, and when the quarantine ends, everyone will almost certainly post even more to Facebook, and its subsidiaries Instagram and WhatsApp, to share the post-quarantine celebration, the author noted, adding that Facebook's stock is arguably attractively priced, with shares down a hair more than the broader market. 4. Major U.S. airlines were urging Treasury officials and the federal government's outside advisers to scrap or revise a proposal that would make part of the $25B earmarked by Congress to help keep workers on the payroll repayable in the form of low-cost loans, Reuters' David Shepardson and Tracy Rucinski reported. Treasury Secretary Steven Mnuchin told the airlines on Friday the government would require them to repay 30% of the grants in low-cost loans over 10 years - with the first five years at 1% interest - before the interest rate would rise. Publicly traded companies in the space include Alaska Air (ALK), American Airlines (AAL), Delta Air Lines (DAL), JetBlue (JBLU), Southwest (LUV), Spirit Airlines (SAVE) and United Airlines (UAL). 5. American Electric Power (AEP), Dominion Energy (D), FirstEnergy (FE) and NextEra (NEE) saw positive mentions in this week's edition of Barron's, while SoftBank (SFTBY) was mentioned cautiously.
ESLT

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16:43 EDT Elbit Systems awarded $20M in contracts to upgrade Hermes 900 UAS - Elbit Systems announced that it was awarded two contracts valued at a total of approximately $20M from Latin American customers to upgrade the capabilities of their Hermes 900 Unmanned Aircraft Systems. Both contracts will be performed within a 12-month period. Under the contracts, the company will integrate satellite communication systems and automatic takeoff and landing systems into the Hermes 900 UAS that the customers are already operating. This upgrade will advance these Medium Altitude Long Endurance UAS to the latest configuration, enabling extension of the operational range to more than 1000km and performing the takeoff and landing autonomously and independent of GPS reception.
INTU

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16:01 EDT Intuit QuickBooks Capital approved as Paycheck Protection Program lender - Intuit announced its subsidiary Intuit Financing is now a non-bank SBA-approved lender for the Paycheck Protection Program, paving the way for small businesses and other eligible applicants to apply for PPP federal relief through the fintech company's QuickBooks Capital systems. As a direct lender, QuickBooks Capital is able to simplify, automate and expedite the PPP application and funding process. QuickBooks Capital can assist applicants in determining eligibility and automating much of the application process. QuickBooks Capital can then facilitate the federal relief application process and, in coordination with the Small Business Association, disburse PPP funds, allowing quicker access to relief.
DXCM...

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15:58 EDT DexCom to join NASDAQ-100 Index beginning April 20, 2020 - Nasdaq (NDAQ) announced that DexCom (DXCM), will become a component of the NASDAQ-100 Index, the NASDAQ-100 Equal Weighted Index and the NASDAQ-100 Ex-Tech Sector Index prior to market open on Monday, April 20, 2020. DexCom will replace American Airlines (AAL) in the indexes.
TSM

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15:57 EDT TSMC reports March revenue NT$113.52B, up 42.4% y/y - TSMC announced its net revenues for March 2020: On a consolidated basis, revenues for March 2020 were approximately NT$113.52B, an increase of 21.5% from February 2020 and an increase of 42.4% from March 2019. Revenues for January through March 2020 totaled NT$310.6B, an increase of 42% compared to the same period in 2019.
PYPL

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15:55 EDT PayPal approved to provide access to Paycheck Protection Program Loans - PayPal announced that the company is now providing access to small business loans through the U.S. Small Business Administration Paycheck Protection Program. This follows approval from the SBA for PayPal to participate in the program as one of the first non-bank institutions.
BGNE

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15:44 EDT BeiGene's tislelizumab receives second approval in China, first in solid tumor - BeiGene announced that its anti-PD-1 antibody tislelizumab has received approval from the China National Medical Products Administration as a treatment for patients with locally advanced or metastatic urothelial carcinoma with PD-L1 high expression whose disease progressed during or following platinum-containing chemotherapy or within 12 months of neoadjuvant or adjuvant treatment with platinum-containing chemotherapy. Following tislelizumab's initial approval in classical Hodgkin's lymphoma by the NMPA in December 2019, this is the second indication approved for tislelizumab, and the first in a solid tumor indication. The supplemental new drug application was previously granted priority review by the Center for Drug Evaluation of the NMPA. The NMPA approval is based on the clinical results from a single-arm, multi-center pivotal Phase 2 trial of tislelizumab in patients in China and South Korea with PD-L1+ locally advanced or metastatic UC who were previously treated with platinum-containing chemotherapy. Among patients who were evaluable for response, with a minimum follow-up of 12 months and a median follow-up of 14 months, the objective response rate as assessed by the independent review committee per RECIST v1.1 criteria was 24.8%, and the complete response rate was 9.9%. The safety data for tislelizumab included in the label is based on 934 patients treated with tislelizumab monotherapy from four clinical trials, including the aforementioned pivotal Phase 2 trial in patients with UC. Most common adverse reactions included rash, fatigue, and increased alanine aminotransferase. Grade 3 or higher adverse reactions occurring in greater than or equal to 1% of patients included: increased gamma-glutamyl transferase, anemia, increased aspartate aminotransferase, increased alanine aminotransferase, pneumonitis, severe skin reactions, and hypokalemia. Like other immune checkpoint inhibitors, tislelizumab could cause immune-related adverse reactions that mainly include pneumonitis, diarrhea and colitis, hepatitis, endocrinopathies, and skin adverse reactions. Occasionally, nephritis, pancreatitis, myocarditis, myositis, and other immune-related adverse reactions were also reported. The recommended dose of tislelizumab is 200 mg administered as an intravenous infusion every three weeks until disease progression or intolerable toxicity.
TGI BA

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15:39 EDT Triumph Group announces furloughs for about 2,300 employees - Triumph Group (TGI) provided an update on the current impact of the coronavirus on the business and the steps the company is taking to mitigate it. Given that Boeing (BA) has extended closure of its Washington state factories indefinitely, and closed its Charleston, South Carolina plant for 14 days, Triumph announced furloughs for approximately 2,300 employees across Triumph plants in the U.S. and Europe for two to four weeks to reduce capacity associated with Boeing Commercial Aircraft programs. These plants will remain operational and continue to support other customer demands. Triumph will provide one week of company pay and will cover the employee share of medical premiums during the furlough period. In addition to the previously announced 500-person reduction in force as part of its austerity measures, Triumph will eliminate approximately 200 full-time positions due to decreased demand. Triumph will pay severance to impacted employees consistent with existing policies. These reductions are expected to be completed by May 1, 2020. To reduce working capital requirements, the company will also adjust its supply chain demand consistent with updated OEM production and aftermarket forecasts. Further workforce adjustments may be required based on site closures or changes in demand for Triumph's products and services. Triumph's liquidity is approximately $500M as of March 31, 2020. Although the situation remains fluid, all but two of Triumph's factories are operational. The company's two facilities in Mexico, which employ approximately 1,900 individuals, are complying with a government mandate for 30-day closure of non-essential operations effective March 31, 2020. Triumph will adjust its plans as government decisions and company policies evolve.
NEOG

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15:35 EDT James Herbert resigns as Neogen chairman, Jim Borel named as successor - Neogen announced today James Herbert has resigned as its chairman, and he has been succeeded by Jim Borel. Herbert will continue to serve on Neogen's Board of Directors until his term expires in October 2020.
LLY

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15:33 EDT Eli Lilly beings clinical testing of therapies for COVID-19 - Eli Lilly announced it has entered into an agreement with the National Institute of Allergy and Infectious Diseases, part of the National Institutes of Health, to study baricitinib as an arm in NIAID's Adaptive COVID-19 Treatment Trial. The study will investigate the efficacy and safety of baricitinib as a potential treatment for hospitalized patients diagnosed with COVID-19, beginning this month in the U.S. with a planned expansion to additional sites including Europe and Asia. Results are expected within the next two months. Baricitinib, an oral JAK1/JAK2 inhibitor marketed as OLUMIANT, is approved in more than 65 countries as a treatment for adults with moderately to severely active rheumatoid arthritis. The U.S. prescribing information includes boxed warnings regarding the use of baricitinib, including warnings about risk for developing serious infections, a risk that may be related to baricitinib's effects on the immune system. Given the inflammatory cascade seen in COVID-19, baricitinib's anti-inflammatory activity has been hypothesized to have a potential beneficial effect in COVID-19 and warrants further study in patients with this infection. Lilly also announced that it will advance LY3127804, an investigational selective monoclonal antibody against Angiopoietin 2, to Phase 2 testing in pneumonia patients hospitalized with COVID-19 who are at a higher risk of progressing to acute respiratory distress syndrome. Ang2 is known to be elevated in ARDS patients and Lilly will test whether inhibiting the effects of Ang2 with a monoclonal antibody can reduce the progression to ARDS or the need for mechanical ventilation in COVID-19 patients. This trial will begin later this month at several U.S. centers. Lilly currently does not anticipate shortages for any of its medicines, including baricitinib, which remains widely available in countries where it is approved. Should research efforts for baricitinib in COVID-19 prove successful, Lilly will continue to create adequate supply to support both appropriate clinical and investigational use.
PACD

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15:28 EDT Pacific Drilling receives Notice of Noncompliance from New York Stock Exchange - On April 7, 2020, Pacific Drilling received notice from the New York Stock Exchange stating that the company does not currently satisfy the minimum share price standard for continued listing of the company's common shares. Specifically, on April 6, 2020, the 30-trading-day average closing price per share of the company's common shares was below $1.00, the minimum average share price required for continued listing on the NYSE under Section 802.01C of the NYSE Listed Company Manual. Under NYSE rules, the company has six months following receipt of the notification to regain compliance with this continued listing standard and avoid delisting. As required by NYSE rules, the company will notify the NYSE that it intends to cure the share price deficiency and is considering all available options to return to compliance. The company can regain compliance at any time during the six-month cure period if on the last trading day of any calendar month during the cure period the company has a closing share price of at least $1.00 and an average closing share price of at least $1.00 over the 30 trading-day period ending on the last trading day of that month. If at the expiration of the cure period, both a $1.00 closing share price on the last trading day of the cure period and a $1.00 average closing share price over the 30 trading-day period ending on the last trading day of the cure period are not attained, the NYSE will commence suspension and delisting procedures.
GILD

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09:38 EDT Gilead says remdesivir improved 68% of COVID-19 patients in 53 person study - Gilead Sciences announced Friday results from a cohort analysis of 53 patients hospitalized with severe complications of COVID-19 who were treated with the investigational antiviral remdesivir on an individual compassionate use basis. The majority of patients in this international cohort demonstrated clinical improvement and no new safety signals were identified with remdesivir treatment. the company said. The detailed results of this analysis were published today in The New England Journal of Medicine. Remdesivir is not yet licensed or approved anywhere globally and has not been demonstrated to be safe or effective for the treatment of COVID-19. 64% of the patients in this cohort were on mechanical ventilation at baseline, including four patients also on extracorporeal membrane oxygenation. Treatment with remdesivir resulted in an improvement in oxygen support class for 68% of patients over a median follow-up of 18 days from the first dose of remdesivir. More than half of patients on mechanical ventilation were extubated and nearly half of all patients were discharged from the hospital following treatment with remdesivir. After 28 days of follow-up, the cumulative incidence of clinical improvement, defined as discharge from the hospital and/or at least a two-point improvement from baseline on a predefined six-point scale, was 84% according to Kaplan-Meier analysis. Clinical improvement was less frequent among patients on invasive ventilation versus noninvasive ventilation and among patients at least 70 years of age. The overall mortality rate in this cohort was 13%. The mortality rate was higher in the subgroup of patients on invasive ventilation. Gilead is conducting two Phase 3 clinical trials of remdesivir, the SIMPLE studies, in countries with high prevalence of COVID-19."Compassionate use data have limitations due to the small size of the cohort, the relatively short duration of follow-up, potential missing data due to the nature of the program and lack of a randomized control group," Gilead added.
RACE

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09:34 EDT Ferrari extends Maranello and Modena manufacturing suspension to May 3 - Ferrari N.V. has extended the suspension of its Maranello and Modena manufacturing activity until May 3, in accordance with the government announcement. The company will continue to pay days of absence for all of those unable to adopt this solution, as it has done since closure of its premises on March 14.
WK

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09:33 EDT Workiva announces departure of Chief Revenue Officer Scott Ryan - Workiva announces that Scott Ryan, Executive Vice President and Chief Revenue Officer, has resigned from the company to pursue other opportunities, effective Friday. In connection with Ryan's departure, Workiva "made additional personnel changes to realign sales leadership and increase sales efficiency." The sales, service and customer success organizations now report directly to Chief Operating Officer Julie Iskow.
CTB

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09:32 EDT Cooper Tire plans to restart tire manufacturing plant in Mexico on April 13 - Cooper Tire & Rubber Company announced Friday that it plans to restart operations at its tire manufacturing plant in El Salto, Mexico beginning April 13. Measures to protect the health and safety of employees, including social distancing, additional cleaning and disinfecting of facilities, restricted visitor access and other necessary steps will be in effect as employees return to work. Announcement of the plant's temporary closure due to coronavirus impacts was made March 21. Cooper plants in the United States, which are located in Findlay, Ohio; Clarksdale and Tupelo, Mississippi; and Texarkana, Arkansas, remain temporarily closed. The company expects these plants to remain temporarily closed for at least another two weeks from now. Cooper plants in Europe also continue to be temporarily closed. The company's plants in China continue to operate. Cooper "believes it has sufficient supply of product in inventory, and the company's distribution centers continue to operate and flow product to customers."
DLTH

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09:28 EDT Duluth announces permanent 10% staff reduction amid COVID-19 pandemic - Duluth Holdings announced "additional measures to ensure its business and financial resiliency during the rapidly escalating impact of the COVID-19 pandemic." As previously reported, the company closed its stores on March 20 to protect its employees and customers. As a result, hourly store employees were temporarily laid off and provided with two weeks of pay. They will have the opportunity to be re-hired as soon as the retail stores are safe to re-open in accordance with state and local regulations. Duluth said it continues to serve its customers through its online business, and its distribution centers remain fully operational. On April 6, the company provided staff at its distribution centers with a $2.50 hourly premium while Duluth Trading stores remain closed. Additional measures to ensure business and financial resiliency include: Six-month pay reduction for senior leadership ranging from 10 to 20 percent; CEO Steve Schlecht will waive all cash compensation for the balance of fiscal 2020; The Board of Directors will forego cash retainers for the second and third quarters; Furloughs of varying lengths with benefits intact for 68% of salaried staff; A permanent 10 percent reduction in corporate staff; All operating expenses are under review including price concessions with vendors and reductions in lease expense for its fleet of retail stores; To curtail capital expenditures, the Company now plans to open four stores in fiscal year 2020, reducing its previously disclosed plan by one store. The company's liquidity position as of April 10 is $85M outstanding on its $130M line of credit and $13M in cash balance.
MFA

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09:26 EDT MFA Financial announces forbearance agreement with counterparties - MFA Financial announced Friday updates with respect to its business operations. On April 10, the company and its repurchase agreement counterparties holding a significant majority of its outstanding repurchase obligations entered into a forbearance agreement. On March 24, MFA had announced that due to the turmoil in the financial markets resulting from the COVID-19 pandemic, the company was engaged in discussions with its financing counterparties regarding forbearance with respect to the company's obligations under its repurchase agreement financing arrangements, which were approximately $9.5B as of March 20. Since the date of that announcement through April 9, the company's indebtedness under such arrangements has decreased to approximately $5.8B. This reduction occurred as a result of sales of certain assets and the payoff of the associated repurchase agreement obligations. MFA added, "In response to the unprecedented market conditions experienced since mid-March, the Company has taken steps to manage and de-lever its portfolio and generate liquidity, particularly in relation to its investments in certain residential mortgage securities." Sales of residential mortgage assets generating proceeds of $3.5B, which were used to reduce the associated repurchase agreement obligations. The company also unwound all of its approximately $4.1B of swap hedging transactions. As of April 9, MFA had total cash balances of $423.4M.
STE

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09:19 EDT Steris announces Emergency Use Authorization for respirator decontamination - Steris announced Friday that the Food and Drug Administration has issued an Emergency Use Authorization for respirator decontamination. The EUA enables healthcare providers to decontaminate N95 Respirators on-site by utilizing certain STERIS V-PRO Low Temperature Sterilization Systems. The EUA allows Steris to temporarily provide a solution for decontaminating compatible N95 or N95-equivalent respirators using the 28-minute Non-Lumen Cycle available on most V-PRO models. STERIS recommends decontaminating masks after each use, up to a maximum of ten times. Ten masks can be decontaminated per cycle.