Stockwinners Market Radar for April 23, 2017 - Earnings, Upgrades downgrades, option trades, Best Stock Advisory Service |
BDX... | Hot Stocks21:24 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. Becton Dickinson (BDX) announced a $24B cash and stock deal to acquire fellow medical technology company C. R. Bard (BCR). The transaction, priced roughly 25% above Bard's closing quote Friday, will shave $300M from annual costs and expand Becton Dickinson's position in "fast growing clinical areas," the companies said. 2. As Wells Fargo's (WFC) April 25 shareholder meeting looms, reports from Reuters and the Wall Street Journal suggested that a full re-election of the bank's board could be less than guaranteed in the wake of its account opening scandal. Elsewhere in corporate governance, United Continental (UAL) CEO Oscar Munoz agreed to drop a chairmanship clause from his contract following the recent passenger "dragging" incident, leaving decisions on the position in the hands of the board. 3. Centrist independent Emmanuel Macron and right-wing leader Marine Le Pen won the first round of France's presidential election Sunday and will now face off in a May 7 runoff vote. 4. This weekend's International Liver Congress brought clinical updates from Albireo Pharma (ALBO), Bristol-Myers Squibb (BMY), Arbutus (ABUS), Merck (MRK) and others. 5. Sarepta (SRPT), Johnson & Johnson (JNJ), MGM Resorts (MGM), Alcoa (AA), O'Reilly Automotive (ORLY), Seritage (SRG) and U.S. bank majors Citi (C), Goldman Sachs (GS), Bank of America (BAC), JPMorgan (JPM), Morgan Stanley (MS) and Wells Fargo saw positive mention in Barron's, while Infosys (INFY) and Harley-Davidson (HOG) were discussed cautiously.
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Hot Stocks20:20 EDT White House budget director: Tax announcement likely to be broad guidance, ideas - Speaking in a Fox News interview Sunday, White House budget director Mick Mulvaney said, "I think what you're going to see on Wednesday is some specific governing principles, some guidance. Also some indication of what the rates are going to be. I don't think you're going to see something -- and I don't think anybody expects us to roll out -- bill language on Wednesday. In fact, we don't want to do that. So what you're going to see on Wednesday for the first time is: Here's what our principles are, here's some of the ideas that we like, some of the ideas we don't like. Here's some of the rates we're talking about." Asked whether the tax reform will be revenue neutral, Mulvaney said, "I don't think we've decided that part yet. Keep in mind, it's a balancing act on that. You can either have a small tax cut that's permanent, or a large tax cut that is short term. I don't think we've decided yet, but you'll know more on Wednesday." Questioned about his recent statement that he doesn't expect a "real plan, specifics, meat on the bone" until June, Mulvaney responded, "I think that's still probably fair. Again, we want to start working -- and have already started working with the committees in the House and the Senate as we try to build some momentum." Reference Link
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Hot Stocks20:02 EDT President Trump: 'Big' tax reform, tax reduction to be announced Wednesday - President Donald Trump tweeted Saturday: "Big TAX REFORM AND TAX REDUCTION will be announced next Wednesday." Reference Link
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BEBE | Hot Stocks19:39 EDT bebe stores to close all locations by end of May - bebe stores disclosed in a regulatory filing Friday: "On April 18, bebe stores entered into a Consulting Agreement with Great American Group, an affiliate of B. Riley & Co., the Company's financial advisor, and Tiger Capital to, among other things, sell all merchandise and inventory owned by the Company and certain of its subsidiaries located in its existing retail stores and certain furnishings, trade fixtures, equipment and improvements to real property with respect to the Stores. We may incur a loss in connection with this sale of our merchandise and inventory, but we cannot estimate such loss at this time... The Company currently anticipates that it will close all of the Stores by the end of May. The Company expects to recognize an impairment charge of approximately $20M, net of deferred rent and other credits, as a result of closing the Stores. This impairment charge will be recorded in the third and fourth quarters of fiscal year 2017."
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CMCSA... | Hot Stocks18:17 EDT Box Office Battle: 'Fate Of The Furious' nears global $1B in second weekend - Comcast's (CMCSA) "The Fate Of The Furious" earned $38.7M over the April 23 weekend, dipped about 61% from its debut and landing near the top end of a $35M-$41M forecast. The eighth entry in "The Fast and the Furious" franchise took an additional $163.4M in international territories, reaching global and U.S. totals of $908M and $164M. BOX OFFICE RUNNERS-UP: Repeating last weekend's standings, Fox's (FOX) "The Boss Baby" grossed $12.8M in its fourth weekend and Disney's "Beauty And The Beast" earned $10M in its sixth. Nature documentary "Born In China," also from Disney, opened roughly in line with estimates at $5.1M. Capping out the top five, Time Warner's (TWX) "Going In Style" added $5M, while the company's small-budget romantic thriller "Unforgettable" debuted in seventh place. Other publicly traded companies in the space include Lionsgate (LGF.A), Sony (SNE) and Viacom (VIA).
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BDX BCR | Hot Stocks17:38 EDT Becton Dickinson names Polen as president, says will lead Bard segment - BD (BDX) announced the appointment of Tom Polen as president of BD, effective immediately. In his new role, Polen will oversee all of BD's operating segments -- the Medical and Life Sciences segments, as well as the new Interventional segment, which will include the C. R. Bard (BCR) businesses following the close of BD's acquisition of Bard. Polen, currently executive vice president and president of the BD Medical Segment, will continue to report to Vince Forlenza, who remains chairman and CEO of BD.
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BDX BCR | Hot Stocks17:30 EDT Becton Dickinson outlines strategic highlights of C.R. Bard acquisition - Expanding on the strategic rationale for its proposed acquisition of C.R. Bard (BCR), Becton Dickinson (BDX) said the deal "will create new opportunities to build on BD's leadership position in medication management and infection prevention with an expanded offering of solutions across the care continuum," adding that "by combining Bard's strong leadership position and innovation pipeline in fast-growing vascular access segments - PICCs, midlines and drug delivery ports - with BD's leadership and innovation in IV drug preparation, dispensing, delivery and administration, the new company will be better positioned to provide end-to-end medication management solutions." Becton Dickinson also expects the merger to "further expand BD's leadership in infection prevention, with offerings positioned to address 75% of the most costly and frequent healthcare associated infections," while Bard's "strong product portfolio and innovation pipeline will increase BD's opportunities in fast growing clinical areas, including peripheral vascular therapy, oncology and bio-surgery." Finally, the company remarked that "BD and Bard will bring to market an expanded portfolio of clinically relevant products, with opportunities to drive near-term revenue synergies outside of the U.S... Bard's strong presence in vascular access and surgery will also help drive sales of the highly complementary CareFusion portfolio outside of the U.S. The combined company will have a large and growing presence in emerging markets, including $1B in annual revenue in China."
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BDX BCR | Hot Stocks17:23 EDT BD sees forming third business segment, says Bard CEO to join board - Commenting on its integration plans, BD (BDX) said it has put in place a plan to ensure a "seamless" integration with Bard (BCR). A designated integration team, comprised of senior members of both organizations, will be led by Bill Tozzi, a seasoned BD executive who most recently served as worldwide president of the Medication and Procedural Solutions business and earlier was corporate controller for BD. At the closing of the transaction, Tim Ring, chairman and chief executive of Bard, and an additional Bard director, are expected to join the BD board, which will be expanded by two directors. "BD is confident in its ability to achieve synergies as it brings together two world class companies and expects to offer opportunities for talented employees to become part of an even more dynamic global leader," the company said. BD (BDX) also announced it expects to create a third segment within the company -- BD Interventional -- where the Bard (BCR) businesses will report both operationally and financially. BD is separately announcing the appointment of Tom Polen, currently executive vice president and president of the BD Medical Segment, as president of BD, effective immediately. In his new role, Polen will oversee BD's Medical and Life Sciences segments, as well as the new Interventional segment.
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BDX BCR | Hot Stocks17:20 EDT BD sees high single-digit EPS accretion in FY19 - "This financially compelling transaction will be immediately accretive and is expected to generate high-single digit accretion to adjusted earnings per share in fiscal year 2019. Approximately $300M of estimated annual, pre-tax, run-rate cost synergies are expected by fiscal year 2020. Separately, BD also expects to benefit from revenue synergies beginning in fiscal year 2019. The transaction is expected to improve BD's gross margins by approximately 300 basis points in fiscal year 2018, increase BD's earnings per share growth trajectory to the mid-teens, and generate strong cash flow," said Becton Dickinson.
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BDX BCR | Hot Stocks17:18 EDT Becton Dickinson says expects to continue buyback suspension - "BD expects to continue the suspension of its share repurchase program. BD is also committed to annual dividend increases while reinvesting in the business to continue to drive long-term growth," said the company.
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BDX BCR | Hot Stocks17:16 EDT Becton Dickinson to acquire C.R. Bard in $24B cash and stock deal - BD (BDX) and C. R. Bard (BCR) announced a definitive agreement under which BD will acquire Bard for $317.00 per Bard common share in cash and stock, for a total consideration of $24B. "The transaction will build on BD's leadership position in medication management and infection prevention with an expanded offering of solutions across the care continuum. Additionally, Bard's strong product portfolio and innovation pipeline will increase BD's opportunities in fast-growing clinical areas," the companies remarked. Under the terms of the transaction, Bard common shareholders will be entitled to receive approximately $222.93 in cash and 0.5077 shares of BD stock per Bard share, or a total of value of $317.00 per Bard common share based on BD's closing price on April 21. At closing, Bard shareholders will own approximately 15% of the combined company. BD expects to contribute approximately $1.7B of available cash to fund the transaction, along with, subject to market conditions, approximately $10B of new debt and approximately $4.5B of equity and equity linked securities issued to the market. Bard shareholders will also receive $8B of BD common stock. BD has also obtained fully committed bridge financing. At closing, BD estimates the combined company will have pro forma leverage of approximately 4.7x and is committed to deleveraging to below 3.0x leverage within three years of closing. The transaction is expected to close in the fall of 2017.
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BDX BCR | Hot Stocks17:11 EDT Becton Dickinson to acquire C.R. Bard for $24B
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AVID MSFT | Hot Stocks16:31 EDT Avid announces strategic cloud alliance with Microsoft - Avid (AVID) announced it has entered into a strategic alliance agreement with Microsoft (MSFT) to "cooperatively develop and market cloud-based solutions and cloud services aimed at the media and entertainment industry." As part of the agreement, Avid has chosen Microsoft Azure as its preferred cloud hosting platform, and will develop and launch a range of Software-as-a-Service and Platform-as-a-Service offerings. "The foundation of the alliance is a comprehensive, multi-year strategic agreement in which both companies will make significant mutual commitments and investments in technology, product development and go-to-market efforts. Under the technology and product development cooperation elements of the agreement, to support Avid's product development efforts and investments, Microsoft will invest additional resources and funding to help accelerate time-to-market for targeted cloud-based solutions and specific Azure-based cloud services for the media and entertainment industry. As part of the commercial cooperation, Avid will offer Microsoft Azure hosting and media services exclusively as an integral part of its own portfolio of cloud-based solutions and cloud services. In addition, the companies will work in close cooperation on the overall go-to-market approach," the company said. The alliance is expected to deliver a "continuous stream" of hosting and services offerings over the next 18 months, with the first wave of offerings slated for a phased release during the second half of 2017.
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OA | Hot Stocks15:32 EDT Orbital ATK says Cygnus spacecraft successfully rendezvous, berths with ISS
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CTRV | Hot Stocks15:30 EDT ContraVir presents data on hepatitis B candidates TXL, CRV431 - ContraVir Pharmaceuticals presented data demonstrating the synergistic antiviral activity from the combination of its two investigational drugs for the treatment of hepatitis B viral infection, tenofovir exalidex and CRV431. In addition, the mode of action of CRV431 was further defined. The data were presented at The International Liver Congress. "As part of today's... poster tour, Dr. Foster provided an overview of a poster entitled, 'The cyclophilin inhibitor CRV431 prevents both cyclophilin A-HBx complex formation and HBV replication.' The poster demonstrated that CRV431 appears to exert an anti-HBV effect by interfering with the binding interaction between HBx and cyclophilin A, thereby reducing HBV replication. In the other poster presentation, 'CRV431 and CMX157: Anti-HBV combination effects in vitro between a cyclophilin inhibitor and a nucleotide prodrug,' Dr. Foster and colleagues reported that TXL and CRV431 synergistically suppress HBV DNA. Overall, the results suggest that combining TXL and CRV431 can be a viable therapeutic drug strategy, and that the two agents' complementary actions may reasonably extend to drugs with other modes of activity," the company said.
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MRK | Hot Stocks15:27 EDT Merck reports new Phase 2 MK-3682B data - Merck announced the first sustained virologic response results 12 weeks after completion of therapy from C-SURGE, an ongoing Phase 2 clinical trial evaluating MK-3682B, the company's investigational triple-combination therapy in treatment-experienced patients with hepatitis C virus genotype 1 infection for whom treatment with approved direct-acting antiviral regimens had failed. The study showed that 100 percent -- 43/43 -- of patients who completed 16 weeks of treatment plus ribavirin achieved SVR12 and 100 percent of patients who completed 24 weeks of treatment achieved SVR12. Results were presented at The International Liver Congress. There were no drug-related serious AEs, and no patients discontinued treatment due to a drug-related AE.
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ABUS | Hot Stocks15:10 EDT Arbutus reports ARB-1467 study data, plans additional trial in 2H - Arbutus Biopharma presented results of the first three cohorts of a Phase II study of its RNAi agent, ARB-1467, at the European Association for the Study of the Liver. "We are very pleased to present updated Phase II results for ARB-1467 that show a consistent reduction in HBsAg in HBV patients regardless of HBeAg status with a favorable safety profile. We look forward to a 3Q17 announcement of the results of Cohort 4, which is evaluating five bi-weekly doses of ARB-1467 with extended monthly dosing out to one year for patients who meet predefined response criteria. Furthermore, we are planning to initiate a new study of ARB-1467 in 2H17 to evaluate longer dosing of ARB-1467 combined with immunomodulatory agent. We believe that this study could pave the way for Phase IIb studies while we continue to advance the rest of our pipeline," the company said, adding that "while this [new] study may include pegylated interferon as the immune boosting component that could lead to later stage development, Arbutus also plans to evaluate other immunomodulatory approaches, such as its proprietary checkpoint inhibitor program, in future combination studies. Arbutus' core protein/capsid inhibitor AB-423... will be ready to be included in studies with RNAi and approved agents in 2018. ARB-1740, a next generation RNAi agent, is being evaluated in an ongoing multi-dosing study in HBV patients, the results of which will be announced in 2H17."
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ACHN JNJ | Hot Stocks15:05 EDT Achillion reports updated data from Phase 2 JNJ-4178 study - Achillion Pharmaceuticals (ACHN) announced Saturday the presentation of updated results from the ongoing phase 2 '604 Study' being conducted by Alios, part of Johnson & Johnson's (JNJ) Janssen companies. Results were presented during the European Association for the Study of the Liver 2017 International Liver Congress. "These results demonstrate that the triple combination of simeprevir, odalasvir and AL-335 has the ability to shorten treatment duration, offer high efficacy and be generally well tolerated in those whose disease is caused by hepatitis C virus genotype 1," the company said. The presentation "demonstrated that JNJ-4178, the three-drug combination of simeprevir, odalasvir and AL-335, was highly effective in treatment naive patients with HCV genotype 1 infection without cirrhosis, achieving 100% SVR24 for treatment durations of both 6 and 8 weeks. The two-drug regimen of odalasvir and AL-335, a combination regimen not anticipated to move forward, achieved 84% SVR24 for treatment duration of 8 weeks in patients with HCV genotype 1 without cirrhosis. The three-drug regimen of simeprevir, odalasvir and AL-335 in HCV genotype 3 patients without cirrhosis achieved an SVR12 of 77% following 12 weeks of therapy, and is also not anticipated to move forward. Genomic sequencing results indicate that despite the presence of multiple NS5A mutations observed at baseline there was no apparent impact on SVR rates. The all-oral combination regimens containing odalasvir and AL-335, with or without simeprevir, were generally safe and well tolerated... Based on these data, JNJ-4178 is being further investigated for the treatment of HCV genotypes 1, 2, 4, 5, and 6," the company said. Achillion noted that results from the Phase 2b study of JNJ-4178 are anticipated during the second half of 2017.
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BMY | Hot Stocks14:59 EDT Bristol-Myers says '036 NASH study meets primary endpoint - Bristol-Myers Squibb announced Saturday data from a Phase 2 study of BMS-986036, an investigational pegylated analogue of human fibroblast growth factor 21 in patients with biopsy-confirmed nonalcoholic steatohepatitis, or NASH. The study achieved its primary endpoint of significant reduction in liver fat versus placebo. Statistically significant improvements were also seen in prespecified exploratory endpoints including biomarkers of fibrosis, metabolic parameters and markers of liver injury. These data were presented at EASL: The International Liver Congress. "These data, along with previously announced Phase 2 data in patients with type 2 diabetes, support further clinical research of BMS-986036 as a potential treatment for NASH. We look forward to sharing these data with health authorities to determine next steps for further study," the company said. Specifically, at Week 16, both dosing regimens of BMS-986036 -- 10 mg daily or 20 mg weekly -- significantly reduced liver fat as measured by MRI-PDFF versus placebo -- 6.8% and 5.2%, respectively, vs. 1.3%. The 10 mg daily dose resulted in 57% of patients reaching greater than or equal to 30% relative risk reduction. The 20 mg weekly dose resulted in 52% of patients reaching greater than or equal to 30% relative risk reduction. Both dosing regimens also improved Pro-C3, magnetic resonance elastography, as well as adiponectin, ALT and AST. Improvements in triglycerides, low density lipoprotein, and high density lipoprotein were also observed in the treatment groups. Overall, BMS-986036 had a favorable safety profile, with no deaths or serious adverse events related to treatment, and no discontinuations due to adverse events.
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ALBO | Hot Stocks14:45 EDT Albireo Pharma reports 'promising' A4250 data, sees Phase 3 trial start in 2H - Albireo Pharma announced that the embargo on its abstract discussing preliminary data from a Phase 2 trial of its lead product candidate A4250 in children with cholestatic liver disease has been lifted and the data was presented Saturday at The International Liver Congress. "The data demonstrated improvement in pruritus and reduction in serum bile acids in most patients, particularly patients with progressive familial intrahepatic cholestasis, after four weeks of treatment with A4250," the company said, adding that "we are currently engaging with regulatory authorities in the United States and Europe with the objective to design a coordinated Phase 3 program in patients with PFIC, which we expect to initiate in the second half of 2017." A4250 reduced mean levels of sBA in all five dose groups, with substantial sBA reductions observed in seven of nine PFIC patients -- ranging from 43 percent to 98 percent. In addition, 14 of 19 patients showed improvement in pruritus using a visual analogue scale. The dose with the greatest improvement showed a mean decrease of 2.86 points from baseline. The trial was not powered for formal statistical analyses. The data showed a significant correlation between reduction in sBA and improvement of pruritus. In addition, no treatment-related serious adverse events were observed, and A4250 was well tolerated. Subsequent to the submission date for ILC, the trial's remaining patients completed the study.
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PG | Hot Stocks14:34 EDT ShaveLogic says wins summary judgement over Gillette - ShaveLogic issued the following statement Friday: "In 2015, shaving giant Gillette Company filed a lawsuit against Dallas-based ShaveLogic, a pioneering start-up in the field of wet-shaving, and four former Gillette employees who were hired or retained by ShaveLogic. It alleged those former employees wrongfully used or disclosed Gillette's confidential information and breached contracts... On Tuesday, April 18, the Massachusetts Superior Court dismissed all Gillette claims against ShaveLogic and its employees. The ruling stated, 'Gillette has been unable to muster any evidence that Defendants used Gillette's confidential information to develop razors for ShaveLogic.' Furthermore, the court allowed ShaveLogic's counterclaims against Gillette to proceed. ShaveLogic filed counterclaims against Gillette for intentionally interfering with prospective business relations, and violating Massachusetts' consumer protection statute." Gillette is a unit of Procter & Gamble.
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ORIG | Hot Stocks14:30 EDT Ocean Rig UDW extends Drill Rigs early consent deadline - Ocean Rig UDW announced Friday that it agreed to extend the term of the early consent deadline under the restructuring support agreement dated March 23 for holders of the senior secured notes issued by the company's direct subsidiary, Drill Rigs Holdings, to accede to the RSA and receive a pro rata portion of the DRH early consent fee of $2.5M. The DRH early consent fee deadline has been extended from April 21 to April 25.
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