Stockwinners Market Radar for June 18, 2017 - Earnings, Upgrades downgrades, option trades, Best Stock Advisory Service

AMZN...

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20:55 EDT On The Fly: Top five weekend stock stories - Catch up on the weekend's top five stories with this list compiled by The Fly: 1. Following news Friday that Amazon (AMZN) will acquire Whole Foods (WFM), Barron's highlighted the "staggering" implications of the deal for competing retailers and grocers such as Wal-Mart (WMT), Target (TGT) and Kroger (KR), while a source quoted by Bloomberg said the ecommerce giant could look to cut prices by, among other possible actions, pushing its own private-label products. 2. This week's Paris Air Show is already generating headlines for the major aircraft makers, including reports of multi-billion dollar orders and product unveils from Airbus (EADSY) and Boeing (BA). 3. Speciality materials and chemicals firm Celanese (CE) and private equity company Blackstone (BX) announced a joint venture to create global acetate tow supplier. 4. Disney (DIS) and Pixar's "Cars 3" topped this weekend's U.S. box offices while "Wonder Woman" from Time Warner (TWX) subsidiary Warner Bros. showed continued staying power. 5. General Electric (GE), Digital Realty (DLR), General Mills (GIS), Genesee & Wyoming (GWR), Rockwell Automation (ROK) and ABB (ABB), as well as banks such as JPMorgan (JPM) and Morgan Stanley (MS) and for-profit education stocks such as American Public Education (APEI), Adtalem (ATGE) and Grand Canyon Education (LOPE) saw positive mention in Barron's. The publication also argued that the rally in technology stocks will resume despite recent turbulence.
BX UTX

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19:13 EDT MB Aerospace announces potential $1B contract with United Technologies - MB Aerospace announced it has signed a new 10-year contract with United Technologies (UTX) with a potential value of up to $1B over the life of the contract. The new contract will see MB Aerospace supply aero-engine components and assemblies for content across the full range of Pratt & Whitney engine programs. MB Aerospace recently secured investment support from Blackstone (BX) when it was acquired by Blackstone and management in a transaction in December 2015.
EADSY BA

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18:48 EDT Airbus unveils A380plus - Airbus (EADSY) published a "development study" for an enhanced version of its A380 jet, the A380plus. The company explained: "The study includes aerodynamic improvements in particular new, large winglets and other wing refinements that allow for up to 4% fuel burn savings. Added to an optimised A380 maintenance programme and the enhanced cabin features first shown at Aircraft Interiors Expo in April, the overall benefit is a 13% cost per seat reduction versus today's A380." Other publicly traded companies in the space include Boeing (BA). Reference Link
GOOG GOOGL

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17:40 EDT Google outlines renewed anti-extremism, anti-terrorism efforts - In an op-ed published in the Financial Times, Google and YouTube outlined four ways they will help tackle extremism. Namely, the companies will increase their use of technology to help identify extremist and terrorism-related videos; "greatly" increase the number of independent experts in YouTube's Trusted Flagger program; take a tougher stance on videos that do not clearly violate its policies; and expand YouTube's role in counter-radicalisation efforts. The companies remarked: "Google and YouTube are committed to being part of the solution. We are working with government, law enforcement and civil society groups to tackle the problem of violent extremism online. There should be no place for terrorist content on our services... The uncomfortable truth is that we, as an industry, must acknowledge that more needs to be done. Now." Reference Link
MRK

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17:33 EDT Merck granted Orphan designation for Keytruda in esophageal carcinoma - The FDA granted Merck Orphan designation for Keytruda in the treatment of esophageal carcinoma. The designation was granted June 15. Reference Link
VRTX

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17:32 EDT Vertex granted Orphan designation for tezacaftor-ivacaftor combination - The FDA granted Vertex Orphan designation for its tezacaftor and ivacaftor combination therapy in the treatment of cystic fibrosis. The designation was granted June 15. Reference Link
LLY

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17:19 EDT Eli Lilly granted Orphan designation for pediatric colitis treatment - The FDA has granted Eli Lilly Orphan designation for its "humanized immunoglobulin G4-variant monoclonal antibody directed against the p19 subunit of interleukin-23" product in the treatment of ulcerative colitis in pediatric patients. The designation was granted June 15. Reference Link
EPZM

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17:18 EDT Epizyme granted Orphan designation for tazemetostat - The FDA has granted Epizyme Orphan designation for its tazemetostat product in the treatment of soft tissue sarcoma. The designation was granted June 15. Reference Link
RARE

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17:17 EDT Ultragenyx granted Orphan designation for burosumab - The FDA has granted Ultragenyx Orphan designation for its burosumab product in the treatment of tumor-induced osteomalacia syndrome. The designation was granted June 15, according to an online notice from the agency. Reference Link
CE BX

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17:16 EDT Celanese, Blackstone to form acetate tow joint venture - Celanese (CE) and funds managed by Blackstone (BX) announced a definitive agreement to form a JV that will create a global acetate tow supplier. Celanese and Blackstone will own 70% and 30% of the JV, respectively. Under the agreement, Celanese will contribute its Cellulose Derivatives unit, including its equity interest in existing JVs with China National Tobacco, and Blackstone will contribute its Rhodia Acetow unit, which it recently acquired from Solvay. The new company is expected to generate 2017 annual pro forma revenue of approximately $1.3B with around 2,400 employees. The JV will have an extended global footprint that includes eight wholly-owned manufacturing facilities and three existing JV sites. "The complementary nature of the tow businesses and a combination of technology expertise will result in synergies mainly from optimization of supply chain networks and procurement of raw materials, energy, equipment, and other services," the companies noted. "This transaction gives us the opportunity to partially monetize Cellulose Derivatives and reallocate significant capital to higher growth businesses within Celanese to accelerate our growth momentum," Celanese commented. The JV will be governed by a board consisting of three directors appointed by Celanese and two by Blackstone. The board, management team, and name of the new company will be decided at a later date. Related to the transaction, commitments for $2.2B of debt have been received by the partners on behalf of the JV. The debt is expected to be supported by cash generation at the JV and is largely non-recourse to Celanese and Blackstone. An initial dividend of approximately $1.6B will be distributed to Celanese following the formation of the JV. "Celanese is expected to deploy the proceeds in value uplift opportunities, including investment in organic growth, acquisitions, share repurchases and debt reduction... Celanese is committed to maintaining its investment grade rating," the companies said. Once approved and upon closing, Celanese is expected to consolidate JV results in its financial statements, subject to Blackstone's minority interest. The companies declined to provide an expected close date, stating that "the formation of the JV is subject to regulatory approvals and customary closing conditions, which will determine the timing of close."
GILD

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17:11 EDT Gilead granted Orphan designation for Tybost - The FDA has granted Gilead Orphan designation for its Tybost product in the treatment of human immunodeficiency virus type 1 infection in pediatric patients. The designation was granted June 15, according to an online notice from the agency. Reference Link
SNY

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17:10 EDT Sanofi granted Orphan designation for alirocumab - The FDA has granted Sanofi-Aventis Orphan designation for its alirocumab product in the treatment of homozygous familial hypercholesterolemia. The designation was granted June 15, according to an online notice from the agency. Reference Link
ALIOF JNJ

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17:08 EDT Actelion granted Orphan designation for macitentan - The FDA granted Actelion (ALIOF) Orphan designation for its macitentan product in the treatment of chronic thromboembolic pulmonary hypertension. The designation was granted June 15, according to an online notice from the agency. Actelion has been acquired by Johnson & Johnson (JNJ). Reference Link
TSLA

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17:04 EDT Elon Musk: 'Promising conversations' with L.A. mayor on tunnel network - Tesla CEO Elon Musk tweeted Sunday: "Promising conversations with @MayorOfLA regarding tunnel network that would carry cars, bikes & pedestrians. Permits harder than technology." Reference Link
BAC...

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16:44 EDT President Trump nominates Clinger as FDIC chairperson - President Donald Trump announced Friday his intent to nominate James Clinger to be a member of the Federal Deposit Insurance Corporation for a term of six years and to be chairperson for a term of five years, effective November 29, 2017. Clinger was most recently chief counsel for the House Committee on Financial Services, having held the position since 2007. In its coverage of the news, the Financial Times noted that the nomination was "greeted with delight" by bank lobbyists. Publicly traded companies in the space include Bank of America (BAC), Citi (C), Goldman Sachs (GS), JPMorgan (JPM) and Morgan Stanley (MS). Reference Link
DIS...

Hot Stocks

16:34 EDT Box Office Battle: 'Cars 3' wins weekend as 'Wonder Woman' shows staying power - Disney (DIS) and Pixar's "Cars 3" earned $53.5M in its U.S. debut over the June 18 weekend, slightly underperforming against estimates of $55M-$58M as well as the $66M launch of its 2011 predecessor. The film, a computer-animated comedy featuring anthropomorphic cars, received an A in audience polls from CinemaScore, holds a critics rating of 65% on reviews aggregator Rotten Tomatoes, and was produced with a reported budget of $175M. In international markets, "Cars 3" grossed $21M. BOX OFFICE RUNNERS-UP: Time Warner's (TWX) "Wonder Woman" added $40.8M in its third weekend, beating expectations for $30M-$35M and showing notable resiliency as it climbs towards a global take of $600M. Taking third place, Lionsgate's (LGF.A) "All Eyez On Me" debuted at $27.1M against forecasts of $15M-$22M. The Tupac Shakur biopic was scored A- in audience polls and holds a 24% critics rating. Rounding out the top five, Comcast's (CMCSA) "The Mummy" grossed $13.9M in its second weekend alongside $53M in foreign receipts, while horror movie "47 Meters Down" from privately held Entertainment Studios opened at $11.5M. Sony's (SNE) "Rough Night," a dark comedy starring Scarlett Johansson and Kate McKinnon, opened in seventh place with a less-than-expected $8.1M. Other publicly traded companies in filmmaking include 21st Century Fox (FOX) and Viacom (VIA).
MDT

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14:43 EDT Medtronic reports real-world data on Reactive ATP therapy - Medtronic announced that, according to a real-world analysis of nearly 8,800 patients presented at EHRA EUROPACE-CARDIOSTIM 2017, its Reactive ATP therapy slows the progression of AF in patients with implanted cardiac devices. Specifically, the retrospective analysis assessed pacemaker, ICD and CRT device data from 8,798 patients followed by the Medtronic CareLink remote monitoring system. Reactive ATP therapy was associated with a statistically significant decrease in AF events compared to a matched control group. Most notably, the Reactive ATP patient group experienced a 38 percent reduction in persistent AF events. This benefit was observed across patient age, sex, and device type.
LLL

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14:37 EDT L3 Technologies says commercial training unit secured $115M in 2017 contracts - L3 Technologies announced that its Commercial Training Solutions business secured contracts in 2017 from commercial operators and airline partners worldwide for commercial aviation training, resourcing and simulation solutions valued at more than $115M. The awards include contracts to deliver airline pilot training programs, airline pilot resourcing, mid-level and classroom devices, and the sale of eight full flight simulators to date in this calendar year.
GE

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14:35 EDT General Electric signs $575M Egyptian rail agreement - GE announced it signed a letter of intent with the Ministry of Transportation and Egyptian National Railways, worth $575M, to supply 100 GE ES30ACi Light Evolution Series Locomotives that can be used for both passengers or freight rail, as well as a 15-year agreement for parts and technical support for GE locomotives in ENR's new and current fleet. The agreement, which is the largest ever between the parties, also includes technical training aimed at improving local capabilities and technical skills.
CY

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14:33 EDT Cypress Semiconductor publicizes settlement proposal with activist group - Cypress Semiconductor issued Saturday the following statement regarding the status of settlement discussions with T.J. Rodgers, who was forced to resign as CEO in April 2016, and CypressFirst: "From the beginning, we recognized that a prolonged proxy contest would be a costly distraction and have attempted to resolve this situation in a constructive manner. In response to stockholder inquiries, we have decided to make public our final settlement proposal to T.J. Rodgers and CypressFirst, which is not subject to any confidentiality restrictions. Our final proposal includes expanding Cypress' board to eight members and immediately adding Dan McCranie and Camillo Martino, who will be appointed to appropriate committees. Importantly, the proposal is consistent with our position that any settlement agreement must include durable and meaningful standstill and non-disparagement provisions, lasting through Cypress' 2019 Annual Meeting."
JUNO

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14:30 EDT Juno Therapeutics reports data from 'TRANSCEND' trial of JCAR017 - Juno Therapeutics presented data from the TRANSCEND trial of JCAR017 in relapsed and refractory aggressive B cell non-Hodgkin lymphoma at the International Conference on Malignant Lymphoma. "High rates of durable responses and the early survival data are especially exciting, as is the emerging safety profile. The majority of TRANSCEND patients experienced no cytokine release syndrome or neurotoxicity at all. While still early, these data suggest that JCAR017 could be administered on an outpatient basis," the company remarked. Data for the DLBCL cohort were presented in two groups, core and full. The core analysis group includes patients that represent the population that Juno plans to move forward into a pivotal trial in the second half of 2017. For the core group, findings include: Overall response rate is 86% and the complete response is 59%. Three-month ORR is 66% and CR is 50%. Of patients in response at three months, 90% continue in response at six months. Early data suggest a dose response relationship at three months. 97% of responding patients are alive and in follow-up as of May 4. 2% experienced severe CRS and 18% experienced severe NT. 66% did not experience any CRS or NT. No deaths were reported from CRS or NT. There was one Grade 5 adverse event of diffuse alveolar damage, which the investigator assessed as possibly related to fludarabine, cyclophosphamide, and JCAR017 treatment, occurring on day 23 in an 82-year-old subject who refused mechanical ventilation for progressive respiratory failure while neutropenic on growth factors and broad spectrum antibiotics and antifungals. This patient had no CRS and Grade 3 neurotoxicity resolution before the Grade 5 event. Regarding manufacturing Juno stated: "Product was available for 98% of patients apheresed... Juno expects commercial production will be accomplished in less than 21 days, and Juno is investing in manufacturing infrastructure to enable a smooth prescribing experience with a reliable delivery time at market entry."
CELG

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14:25 EDT Celgene reports updated data from 'MAGNIFY' study of Revlimid - Celgene announced results from an interim analysis of MAGNIFY, a phase IIIb study of REVLIMID plus rituximab combination therapy in patients with relapsed or refractory marginal zone lymphoma. Results were presented at the International Conference on Malignant Lymphoma, and expanded upon data presented earlier in the month at the American Society of Clinical Oncology meeting. At ASCO, interim data were presented from an analysis of a subset of patients from the MAGNIFY study with relapsed or refractory FL with early relapse and double-refractory disease. Data being presented at ICML in a separate analysis focused on patients with MZL, including nodal MZL, splenic MZL and mucosa-associated lymphoid tissue lymphoma. At a median follow-up of 13.8 months from initiation of therapy with the R2 combination, evaluable patients with MZL achieved an ORR of 66% with a CR/CRu rate of 44%. Evaluable nodal MZL patients had an ORR of 57% with a CR/CRu rate of 57%. Evaluable splenic MZL patients had an ORR of 63% with a CR of 25%; and evaluable MALT patients had an ORR of 80% with a CR/CRu rate of 40%. Median duration of response was not reached for any group. The most common grade 3 or 4 adverse events observed in patients with MZL were neutropenia, thrombocytopenia and leukopenia.
MGNX

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14:15 EDT MacroGenics reports updated Phase 1 data on MGD010 - MacroGenics announced the presentation of updated data from its Phase 1 study of MGD010 at the European League Against Rheumatism Annual European Congress of Rheumatology. The Company highlighted the immunomodulatory impact of MGD010 on the response to hepatitis A vaccination in normal healthy subjects. The data demonstrate that by pharmacologically exploiting the activity of the checkpoint molecule CD32B in combination with the B-cell receptor CD79B component, a single dose administration of MGD010 at either 3 or 10 mg/kg delivers an immunomodulatory effect that counters B-cell function, the company said. There were no CTCAE grade 3 or higher adverse events related to MGD010. Consistent with prior observations, ex vivo flow cytometric analysis confirmed dose-dependent MGD010 binding to peripheral B cells without B-cell depletion, accompanied by decreased surface BCR and CD40 expression as well as a decrease in total serum IgM levels. Compared to the placebo group, reduced HAV seroconversion rates were observed in subjects treated with MGD010, with significantly lower HA-specific IgG levels. "These results provide compelling rationale for further development of this therapeutic modality for autoimmune disorders," the company remarked.
BKE

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14:12 EDT The Buckle warns of data security incident - The Buckle issued the following statement Friday: "We became aware that The Buckle, Inc. was a victim of a security incident in which a criminal entity accessed some guest credit card information following purchases at some of our retail stores. We immediately launched a thorough investigation and engaged leading third-party forensic experts to review our systems and secure the affected part of our network. Through that investigation we learned that our store payment data systems were infected with a form of malicious code, which was quickly removed. Based on the forensic investigation, we believe that no social security numbers, email addresses or physical addresses were obtained by those criminally responsible. There is also no evidence that the buckle.com website or buckle.com guests were impacted. All Buckle stores had EMV -- "chip card" -- technology enabled during the time that the incident occurred and we believe the exposure of cardholder data that can be used to create counterfeit cards is limited. However, it is possible that certain credit card numbers may have been compromised... We are cooperating fully with card brands and forensic investigation services."