Stockwinners Market Radar for November 17, 2019 - Earnings, Upgrades downgrades, option trades, Best Stock Advisory Service |
HPQ... | Hot Stocks20:56 EST Fly Intel: Top five weekend stock stories - Catch up on the weekend's top five stories with this list compiled by The Fly: 1. HP Inc. (HPQ) announced that its board unanimously rejected an unsolicited proposal from Xerox Holdings Corporation (XRX) to acquire the company, but added that it recognized "the potential benefits of consolidation," and was "open to exploring whether there is value to be created for HP shareholders through a potential combination with Xerox." 2. Barrick Gold Corporation (GOLD) announced it reached an agreement to sell its 50% interest in Kalgoorlie Consolidated Gold Mines in Western Australia to Saracen Mineral Holdings Limited for a total consideration of $750M in cash. The transaction is expected to be completed in Q4 of 2019 and is subject to customary closing conditions. 3. PG&E (PCG) announced it is monitoring a potentially strong weather event for Wednesday, November 20. The company added that "projections reflect a possible weather event similar to previous PSPS events that impacted about 180,000 customers." 4. Twentieth Century Fox's (FOX, FOXA) auto racing biographical drama "Ford v Ferrari" easily outperformed domestic estimate of earning ~$22M in its opening weekend, earning $31M. However, Sony Pictures' (SNE) action comedy reboot "Charlie's Angels" finished in third place in its opening weekend with $8.6M domestically, well below expectations of a $13M open. 5. Broadridge Financial Solutions (BR) and Medtronic (MDT) saw positive mentions in this week's edition of Barron's, while Disney (DIS) and Berkshire Hathaway (BRK.A, BRK.B) saw negative mentions.
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RCEL | Hot Stocks20:39 EST Avita Medical appoints David McIntyre CFO - AVITA Medical announced the appointment of David McIntyre as CFO effective November 18. McIntyre will assume responsibility for overseeing the global finance and investor relations functions and will be based in AVITA's Valencia office in California. Interim CFO Tim Rooney will continue in his role as AVITA Medical's Chief Administrative Officer with responsibility for global operations and supply chain management, program management, human resources, and information technology. Most recently, McIntyre served as a partner with Apple Tree Partners.
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JEF | Hot Stocks20:13 EST Jefferies Financial Group to sell 31% interest in National Beef to Marfrig - Jefferies Financial Group announced that it has entered into a definitive agreement to sell its remaining 31% interest in National Beef to Marfrig Global Foods, or Marfrig. This follows its original sale to Marfrig of a 48% interest in National Beef in June 2018. Under the terms of this agreement, Jefferies will realize a total of $970M in cash, including $860M of proceeds from Marfrig and $110M from final distributions from National Beef. Closing is expected on or about November 30, subject to limited and customary closing conditions. The transaction will result in a pre-tax gain of approximately $210M being recognized by Jefferies.
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NIO | Hot Stocks20:11 EST NIO Inc. appoints Wei Feng CFO - NIO Inc. announced that Wei Feng is joining the company as its new CFO, effective November 18. Prior to joining NIO, Feng served as managing director and head of the auto and auto parts research team at China International Capital Corporation.
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GOLD | Hot Stocks20:09 EST Barrick Gold to sell 50% stake in Australian mine for $750M in cash - Barrick Gold Corporation (GOLD) announced it has reached an agreement to sell its 50% interest in Kalgoorlie Consolidated Gold Mines in Western Australia to Saracen Mineral Holdings Limited for a total consideration of $750M in cash. The transaction is expected to be completed in Q4 of 2019 and is subject to customary closing conditions.
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ESPR | Hot Stocks15:11 EST Esperion presents pooled analyses from four Phase 3 bempedoic acid studies - Esperion announced that pooled analyses from four Phase 3 clinical studies of bempedoic acid were presented at the American Heart Association, or AHA, Scientific Sessions in Philadelphia. Bempedoic acid is being developed as a convenient, once-daily, oral therapy for the treatment of patients with elevated low-density lipoprotein cholesterol added onto maximally tolerated statin therapy. Bempedoic acid and the bempedoic acid 180 mg + ezetimibe 10 mg fixed dose combination tablets' new drug applications are currently under regulatory review by the FDA and the marketing authorisation applications are currently under centralized review by the European Medicines Agency, or EMA. "We are very pleased with the pooled analyses from the Phase 3 LDL-C lowering clinical development program showing bempedoic acid not only lowered LDL-C by 25% but also reduced HbA1c by 0.19% in 1,134 patients with diabetes," said Tim Mayleben, CEO of Esperion. "These pooled analyses further support our confidence that bempedoic acid could be a convenient and important, oral, once-daily drug for the millions of patients on maximally tolerated statin therapy who need additional LDL-C lowering."
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PCG | Hot Stocks15:06 EST PG&E monitoring potential weather event that could lead to power shutoffs - Pacific Gas and Electric Company operational and meteorological teams are monitoring a potentially strong offshore wind event on Wednesday, November 20. The forecast remains uncertain, but there is a possibility that the weather could prompt a Public Safety Power Shutoff, or PSPS, for some customers in the Sierra Foothills, North Valley and North Bay. During late fall, PG&E's service territory typically experiences dry vegetation that are ripe for igniting or spreading a wildfire. But dry vegetation conditions have worsened further due to above average temperatures for this time of year, the lack of rain and the recent series of extreme wind events. Both the forecast and the scope of the weather event remain very fluid three days ahead of the event. At present, projections reflect a possible weather event similar to previous PSPS events that impacted about 180,000 customers.
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XRX HPQ | Hot Stocks15:04 EST HP unanimously rejects unsolicited Xerox proposal - HP Inc. (HPQ) announced that its board has unanimously rejected the unsolicited proposal from Xerox Holdings Corporation (XRX) to acquire the company. The HP board sent a letter to Xerox CEO John Visentin, stating, "Our board of directors has reviewed and considered your unsolicited proposal dated November 5, 2019 at a meeting with our financial and legal advisors and has unanimously concluded that it significantly undervalues HP and is not in the best interests of HP shareholders. In reaching this determination, the board also considered the highly conditional and uncertain nature of the proposal, including the potential impact of outsized debt levels on the combined company's stock. We have great confidence in our strategy and our ability to execute to continue driving sustainable long-term value at HP. In addition, the board and management team continue to take actions to enhance shareholder value including the deployment of our strong balance sheet for increased repurchases of our significantly undervalued stock and for value-creating M&A. We recognize the potential benefits of consolidation, and we are open to exploring whether there is value to be created for HP shareholders through a potential combination with Xerox. However, as we have previously shared in connection with our prior requests for diligence, we have fundamental questions that need to be addressed in our diligence of Xerox. We note the decline of Xerox's revenue from $10.2B to $9.2B (on a trailing 12-month basis) since June 2018, which raises significant questions for us regarding the trajectory of your business and future prospects. In addition, we believe it is critical to engage in a rigorous analysis of the achievable synergies from a potential combination. With substantive engagement from Xerox management and access to diligence information on Xerox, we believe that we can quickly evaluate the merits of a potential transaction. We remain ready to engage with you to better understand your business and any value to be created from a combination."
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AZN | Hot Stocks13:17 EST Data shows AstraZeneca's Brilinta reduces risks of clinically relevant bleeding - New results from a pre-specified subgroup analysis of the TWILIGHT trial showed that Brilinta monotherapy reduced the risk of clinically relevant bleeding compared to dual antiplatelet therapy, or DAPT, over 12 months in high-risk patients with non-ST elevation acute coronary syndromes. Results of the TWILIGHT sub-analysis were presented in a late breaker oral presentation on November 17 at the American Heart Association, or AHA, Scientific Sessions 2019 in Philadelphia. Danilo Verge, VP Global Medical Affairs, Cardiovascular, Renal and Metabolism said, "The TWILIGHT trial provided important information about the longer-term management of high-risk patients who had undergone PCI. In this pre-specified subgroup analysis of patients with NSTE-ACS enrolled in TWILIGHT, treatment with ticagrelor monotherapy, without aspirin, after three months of DAPT was associated with a lower risk of bleeding compared with standard 12 months of dual antiplatelet therapy with ticagrelor plus aspirin."
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LLY | Hot Stocks13:11 EST Analysis shows Jardiance decreased risk of hospitalization for heart failure - A new interim analysis of three-year data from the EMPagliflozin compaRative effectIveness and SafEty, EMPRISE, real-world study on effectiveness shows that Jardiance was associated with a decreased risk of hospitalization for heart failure and a similar risk of non-fatal atherosclerotic cardiovascular events compared with DPP-4 inhibitors and GLP-1 receptor agonists. The interim analysis included 190,000 adults in the U.S. with type 2 diabetes with and without cardiovascular disease. The results were shared on behalf of Boehringer Ingelheim and Eli Lilly and Company (LLY) at the American Heart Association Scientific Sessions 2019 in Philadelphia.
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AZN | Hot Stocks13:09 EST AstraZeneca says data shows Farxiga reduces risks in heart failure patients - AstraZeneca announced new data from five additional analyses of the landmark Phase III DAPA-HF trial, which showed that Farxiga reduced the risk of the primary composite outcome of worsening heart failure, or HF, defined as hospitalization or an urgent visit, or death from cardiovascular, or CV, causes versus placebo, when added to standard of care. DAPA-HF is the first outcomes trial with an SGLT2 inhibitor investigating the treatment of HF in patients with reduced ejection fraction, with and without type 2 diabetes, or T2D. The new analyses showed the consistency of these results across patient subgroups with and without T2D, an early onset of effects, and improvement in patient-reported outcomes of HF-related health status. These data were presented at the American Heart Association, or AHA, Scientific Sessions in Philadelphia. Elisabeth Bjork, senior VP, Head of Late-stage Development, Cardiovascular, Renal and Metabolism, BioPharmaceuticals R&D, said: "Heart failure affects approximately 64M people around the world and about half of those patients will die within five years of diagnosis. These new analyses from the DAPA-HF trial reinforce the science behind FARXIGA as clinically significant across heart failure patient populations and suggest the potential to improve the current standard of care for millions of these patients."
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BA | Hot Stocks13:05 EST Boeing, Biman announce order for two 787-9 Dreamliner jets - Boeing and Biman Bangladesh Airlines announced at the 2019 Dubai Airshow that the carrier is expanding its 787 Dreamliner fleet with two additional airplanes valued at $585M at list prices. The purchase - recorded in October as an unidentified order on Boeing's website - complements Biman's fleet of 787-8 jets with the larger and longer-range 787-9 variant.
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BBIO EIDX | Hot Stocks13:04 EST BridgeBio, Eidos present 'positive' data from Phase 2 clinical trial of AG10 - BridgeBio Pharma (BBIO) and Eidos Therapeutics (EIDX) presented positive data from the companies' ongoing Open Label Extension of the Phase 2 clinical trial studying AG10 in patients with symptomatic transthyretin amyloidosis cardiomyopathy. ATTR-CM is a progressive and fatal disease that is an under recognized cause of heart failure. The data were presented in a late-breaking featured science oral presentation at the American Heart Association, or AHA, Scientific Sessions in Philadelphia, Pennsylvania. "This update from our Phase 2 OLE demonstrated continued tolerability of AG10 in patients with advanced ATTR-CM. We also observed meaningfully lower rates of mortality and cardiovascular hospitalizations than what would be expected for untreated ATTR-CM patients with similar disease severity," said Jonathan Fox, Chief Medical Officer of Eidos. "These encouraging data continue to support the development of AG10 as a potentially best-in-class treatment for ATTR-CM patients."
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CLBS | Hot Stocks13:01 EST Caladrius reports 'positive' results for CLBS16 from ESCaPE-CMD trial - Caladrius Biosciences presented results from the ESCaPE-CMD trial of Caladrius's autologous CD34+ cell therapy, CLBS16, at the American Heart Association Scientific Sessions 2019. Data showed highly statistically significant improvement in coronary flow reserve correlating with symptom relief for patients with coronary microvascular dysfunction after a single intracoronary injection of CLBS16. The results for patients who have completed the six-month follow-up to date were presented, with the results from the remaining patients expected by the end of 2019. "CLB16 represents a potential breakthrough for the treatment of CMD, a condition that affects millions in the U.S. and that disproportionately afflicts women. This is the first time that a therapy has shown the ability to durably increase coronary flow reserve and potentially reverse CMD after a single dose. These reported results clearly support the premise that manageable cell-based tissue regeneration is possible in patients with CMD," said David Mazzo, CEO of Caladrius. "The reported results from the ESCaPE-CMD trial bring us one step closer to realizing the promise of CD34+ cell therapy to augment microvasculature in the heart enabling the restoration of health rather than simply management of disease."
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KNSA | Hot Stocks12:59 EST Kiniksa presents Rilonacept final Phase 2 clinical data - Kiniksa Pharmaceuticals reported final data from an open-label Phase 2 clinical trial of rilonacept, a weekly, subcutaneously-injected, recombinant fusion protein that blocks IL-1alpha and IL-1beta signaling. The data were included in a poster presentation at the American Heart Association, or AHA, Scientific Sessions 2019. The Phase 2 data provided first evidence that rilonacept treatment improved clinically meaningful outcomes associated with the unmet medical need in recurrent pericarditis. "The final Phase 2 data showed the potential for rilonacept to improve clinically meaningful outcomes associated with unmet need in recurrent pericarditis," said Sanj Patel, CEO of Kiniksa. "Rilonacept treatment in the Phase 2 trial led to a rapid resolution of recurrent pericarditis episodes that was sustained throughout the 6-month study as well as an improvement in overall quality of life scores. Treatment with rilonacept also led to a decrease in the annualized incidence of pericarditis episodes and importantly supported the discontinuation of corticosteroids without pericarditis recurrence. These data further confirm our confidence in the design of RHAPSODY, our pivotal Phase 3 trial of rilonacept in recurrent pericarditis, for which we expect top-line data in the second half of 2020."
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MDCO | Hot Stocks12:57 EST The Medicines Co's ORION-10 study of Inclisiran met primary, secondary endpoints - The Medicines Company announced detailed results from ORION-10, the second of three pivotal 18-month low-density lipoprotein cholesterol, or LDL-C, lowering Phase 3 clinical studies of inclisiran, an investigational twice-yearly therapy to reduce LDL-C and the first and only cholesterol-lowering treatment in the siRNA class. In ORION-10, twice-yearly dosing with inclisiran sodium 300 mg met all primary and secondary efficacy endpoints, was well-tolerated and again demonstrated an excellent safety profile. Full study results were presented during a late-breaking science session at the American Heart Association, or AHA, Scientific Sessions in Philadelphia. "Cumulative exposure to high LDL-C levels presents a significant risk of future heart attacks and strokes for millions of people, particularly those with ASCVD," said study principal investigator R. Scott Wright, M.D., Professor of Medicine, Consultant in Cardiology, Mayo Clinic in Rochester, Minnesota. "The data from ORION-10 show that inclisiran lowers LDL-C significantly and sustains reductions over a six-month period with a safety profile similar to placebo."
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AMGN | Hot Stocks12:54 EST Amgen analysis shows benefit of Repatha in high risk patients - Amgen announced a new analysis from the Repatha cardiovascular outcomes FOURIER study that evaluates the effectiveness of Repatha in patients who have suffered a recent myocardial infarction, or MI. The analysis showed that patients who experienced a recent MI were at higher risk of subsequent cardiovascular, or CV, events compared to patients who had an MI over a year ago. In the analysis, the risk reduction for experiencing a heart attack, stroke or CV death, in Repatha-treated patients treated within one year post MI was 25% compared to 15% in those patients with a more distant MI. The results will be presented at the American Heart Association Annual Scientific Sessions in Philadelphia on Monday, November 18.
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CNI | Hot Stocks12:52 EST Canadian National receives strike notice from train conductor union - CN said that the Teamsters Canadian Rail Conference - Conductors, Trainpersons and Yardpersons, or TCRC-CTY, which represents approximately 3,200 CN employees who work as train conductors and railyard coordinators only in Canada, has given the company a 72-hour notice of its intention to strike as of 00:01 hours Eastern Standard Time on November 19. Rob Reilly, executive VP and COO of CN, said: "We continue to negotiate in good faith to reach a fair agreement before the strike deadline. In the spirit of protecting the Canadian economy, we have offered the union binding arbitration and they have declined. If a settlement cannot be reached this weekend, we will once again encourage the union leadership to accept binding arbitration as an alternative to disrupting the Canadian economy. We remain committed to constructive talks to reach an agreement without a work stoppage."
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ADAP | Hot Stocks12:51 EST Adaptimmune data confirms ADP-A2M4 delivers clinical benefit - Adaptimmune Therapeutics presented updated data from people with synovial sarcoma treated in the ongoing Phase 1 trial with ADP-A2M4. The oral presentation by Brian Van Tine, MD, PhD of Washington University School of Medicine in St. Louis, took place at the Connective Tissue Oncology Society, or CTOS, annual meeting in Tokyo, Japan. The presentation was an update of the data that Dr. Van Tine presented at ESMO on September 30. Out of the 14 patients with synovial sarcoma who have been treated in the expansion phase of this trial and have post-baseline scans, to date, seven have had clinical responses, representing an overall response rate of 50%. Thirteen patients showed clinical benefit with best overall responses of PR or stable disease - representing a disease control rate of 93%. "This updated data set confirms that ADP-A2M4 continues to deliver clinical benefit, including RECIST responses, to patients with synovial sarcoma. It has also galvanized the support we have received from the sarcoma community, allowing us to rapidly open multiple sites and screen patients for the Phase 2 SPEARHEAD-1 trial," said Elliot Norry, Adaptimmune's acting Chief Medical Officer. "We expect that all sites for SPEARHEAD-1 will be open by the end of the first quarter in 2020, marking another step toward our goal of making this treatment available commercially to people with sarcoma in 2022."
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CELG BMY | Hot Stocks12:47 EST Bristol-Myers sees no further extension for Celgene notes due to merger closing - Bristol-Myers Squibb Company (BMY) announced that it currently expects there will be no further extension of the expiration date of the offers to exchange notes issued by Celgene Corporation (CELG) for up to $19.85B aggregate principal amount of new notes to be issued by Bristol-Myers Squibb Company and cash and the related consent solicitations being made by Bristol-Myers Squibb on behalf of Celgene to adopt certain proposed amendments to the indentures governing the Celgene notes. As previously announced, the exchange offers and consent solicitations are currently scheduled to expire on November 20. The closing of the merger is expected to occur on November 20. As a result, Bristol-Myers Squibb currently expects that there will be no further extension of the expiration date as it is anticipated that the merger will be completed on the expiration date. The settlement date for the exchange offers is expected to occur on November 22, 2019.
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