Stockwinners Market Radar for February 27, 2022 - Earnings, Upgrades downgrades, option trades, Best Stock Advisory Service

SONY...

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20:09 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. The BP (BP)board announced that BP will exit its shareholding in Rosneft. BP has held a 19.75% shareholding in Rosneft since 2013. Additionally, BP chief executive officer Bernard Looney is resigning from the board of Rosneft with immediate effect. The other Rosneft director nominated by BP, former BP group chief executive Bob Dudley, is similarly resigning from the board. BP is expected to give rise to a non-cash adjusting item charge at the time of the first quarter 2022 results, representing the difference between the fair value of BP's Rosneft shareholding at 31 March 2022 and the carrying value of the asset. At the end of 2021 this carrying value stood at around $14 billion. In addition, the change is expected to result in non-cash adjusting item charge, principally arising from foreign exchange losses accumulated since 2013 that under IFRS were previously recorded directly in equity rather than the income statement. At the end of 2021 these totaled around $11 billion, and this adjustment will not impact equity. The change in accounting treatment also means that BP will no longer recognize a share in Rosneft's net income, production and reserves. BP will no longer report Rosneft as a separate segment from the first quarter 2022 results. 2. UPS (UPS) and FedEx (FDX) have said they are halting delivery service to Russia and Ukraine in light of the Russian invasion of its neighbor, Reuters reported. Both inbound and outbound services have been suspended to Ukraine, as well as deliveries to destinations in Russia, the companies said in online statements seen on Sunday. Meanwhile, Alphabet's (GOOGL) Google barred on Saturday Russia's state-owned media outlet RT and other channels from receiving money for ads on their websites, apps and YouTube videos, similar to a move by Facebook (FB) after the invasion of Ukraine, Reuters' Paresh Dave reported. Citing "extraordinary circumstances," Google's YouTube unit said it was "pausing a number of channels' ability to monetize on YouTube." These included several Russian channels affiliated with recent sanctions, such as those by the European Union. 3. As one of the world's leading tire makers, Goodyear Tire (GT) stands to benefit from the auto industry's transition to electric vehicles, Andrew Bary wrote in this week's edition of Barron's. Shares of Goodyear look appealing after being hammered following its fourth-quarter earnings report on Feb. 11, the author contended, adding that unlike the major auto makers that are being disrupted by the shift to electric vehicles, tire makers stand to benefit quickly. 4. Sony's (SONY) "Uncharted" won this weekend's box office with a $23.3M from 4,275 locations in its second outing for a domestic cume of $83.4M. The movie is based on the popular PlayStation game series and stars Tom Holland and Mark Wahlberg. 5. Evoqua Water Technologies (AQUA), Deere (DE), American Water Works (AWK), Southern Company (SO), CarMax (KMX), and Constellation Brands (STZ) saw positive mentions in this week's edition of Barron's.
DAL

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16:48 EST Delta suspended codeshare with Russian national airline, Aeroflot - On Friday, Delta announced it had withdrawn its codeshare services operated in conjunction with Russian national airline, Aeroflot, effective immediately. "We have removed our code from Aeroflot-operated services beyond Moscow's Sheremetyevo Airport and removed Aeroflot's code from Delta-operated services from Los Angeles and New York-JFK. Accommodations will be made for customers affected by these changes. Delta does not operate services to Ukraine or Russia," Delta stated in a post to its news hub site on Friday morning. Reference Link
BP

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16:47 EST BP to exit Rosneft shareholding, CEO to resign from Rosneft board - The BP board announced that BP will exit its shareholding in Rosneft. BP has held a 19.75% shareholding in Rosneft since 2013. Additionally, BP chief executive officer Bernard Looney is resigning from the board of Rosneft with immediate effect. The other Rosneft director nominated by BP, former BP group chief executive Bob Dudley, is similarly resigning from the board. As a result of the resignations of BP's nominated directors, BP has determined that it no longer meets the criteria set out under International Financial Reporting Standards for having "significant influence" over Rosneft. BP will therefore no longer equity account for its interest in Rosneft, treating it now as a financial asset measured at fair value. This will result in two material changes to BP's financial reporting and finances in the results for the first quarter of 2022. First, it is expected to give rise to a non-cash adjusting item charge at the time of the first quarter 2022 results, representing the difference between the fair value of BP's Rosneft shareholding at 31 March 2022 and the carrying value of the asset. At the end of 2021 this carrying value stood at around $14 billion. Second, in addition, the change is expected to result in non-cash adjusting item charge, principally arising from foreign exchange losses accumulated since 2013 that under IFRS were previously recorded directly in equity rather than the income statement. At the end of 2021 these totaled around $11 billion, and this adjustment will not impact equity. The change in accounting treatment also means that BP will no longer recognize a share in Rosneft's net income, production and reserves1. BP will no longer report Rosneft as a separate segment from the first quarter 2022 results. As a result of the accounting changes, and excluding Rosneft from base year and future periods, bp now expects to continue, as before, to deliver a 7-9% EBIDA per share CAGR between the second half of 2019/first half of 2020 through 2025 at oil prices of $50-$60 per barrel based on BP's planning assumptions; EBITDA from resilient hydrocarbons and group to be around $2 billion lower in 2025, at around $31 billion and $38 billion respectively. As bp now is exiting its interest in Rosneft, it has removed Rosneft dividend payments from its financial frame. However, BP says it remains confident in the flexibility and resilience of its financial frame, underpinned by an average 2021-2025 cash balance point of around $40 per barrel. This includes reaffirming the guidance regarding its expectations for shareholder distributions - dividends and buybacks - out to 2025 that was given with its 2021 full year results in February 2022.
PDCE

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15:41 EST PDC Energy reschedules 2021 Q4, year-end conference call - PDC Energy announced plans to reschedule its conference call to discuss its fourth quarter and full-year 2021 operating and financial results. The company now plans to issue its news release before market open on Monday, February 28, followed thereafter by additional materials.
PLX

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15:39 EST Protalix, Chiesi Global Rare Diseases announce submission of MAA for PRX-102 - Protalix BioTherapeutics and Chiesi Global Rare Diseases, a business unit of Chiesi Farmaceutici S.p.A., announced the submission of a Marketing Authorization Application via centralized procedure to the European Medicines Agency for pegunigalsidase alfa for the proposed treatment of adults with Fabry disease, and the subsequent validation of the MAA by the EMA.
SNY REGN

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15:37 EST Regeneron, Sanofi announced detailed results for second Phase 3 trial - Regeneron Pharmaceuticals (REGN) and Sanofi (SNY) announced positive detailed results from a second Phase 3 trial that showed Dupixent 300 mg weekly significantly improved the signs and symptoms of eosinophilic esophagitis at 24 weeks compared to placebo in patients 12 years and older. Topline results from the Dupixent 300 mg weekly arm of the trial, which enrolled 80 patients in the Dupixent group and 79 patients in the placebo group, were announced in October 2021 and confirm results from the first Phase 3 trial. The co-primary endpoints at 24 weeks assessed patient-reported measures of difficulty swallowing, and esophageal inflammation. Data presented at the 2022 AAAAI Annual Meeting showed that patients treated with Dupixent 300 mg weekly experienced the following changes by week 24 compared to placebo: 64% reduction in disease symptoms from baseline compared to 41% for placebo. Patients receiving Dupixent experienced a 23.78 point improvement on the DSQ, compared to a 13.86 point improvement for placebo; baseline DSQ scores were approximately 38 and 36 points, respectively. Nearly 10 times as many patients receiving Dupixent achieved histological disease remission: 59% of patients achieved histological disease remission compared to 6% of patients receiving placebo; mean baseline peak levels were 89 and 84 eos/hpf, respectively. The safety results of the trial were generally consistent with the known safety profile of Dupixent in its approved indications. For the 24-week treatment period, overall rates of adverse events were 84% for Dupixent 300 mg weekly and 71% for placebo. No imbalance was observed in rates of treatment discontinuation due to adverse events between Dupixent and placebo groups prior to week 24. The trial also found that significantly more patients treated with Dupixent 300 mg every two weeks reduced their esophageal eosinophilic count to the normal range compared to placebo; however, there was not a significant improvement in dysphagia symptoms.
SNY REGN

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15:33 EST Regeneron, Sanofi announce detailed results for Dupixent in patients with CSU - Regeneron Pharmaceuticals (REGN) and Sanofi (SNY) announced detailed results for Dupixent in patients with chronic spontaneous urticaria who are biologic-naive. The pivotal trial showed adding Dupixent to standard-of-care antihistamines significantly reduced itch and hives at 24 weeks compared to antihistamines alone in this investigational setting. Topline results from the randomized, double-blind, placebo-controlled pivotal trial, which met primary and all key secondary endpoints at week 24, were announced in July 2021. Data presented at the 2022 AAAAI Annual Meeting showed that patients who added Dupixent to standard-of-care antihistamines nearly doubled the reduction in itch and urticaria activity compared to standard-of-care alone with continuous improvement out to 24 weeks. The trial demonstrated safety results similar to the known safety profile of Dupixent in its approved dermatology indications. For the 24-week treatment period, overall rates of adverse events were generally similar between the Dupixent and placebo groups. The most common adverse event was injection site reactions. The potential use of Dupixent in CSU is currently under clinical development, and the safety and efficacy have not been fully evaluated by any regulatory authority.
AMGN

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15:29 EST Amgen announces data from pooled post-hoc analysis of NAVIGATOR, PATHWAY trials - Amgen announced results from a pooled post-hoc analysis of the pivotal NAVIGATOR Phase 3 and PATHWAY Phase 2b trials showed TEZSPIRE demonstrated reductions in the annualized asthma exacerbation rate across biomarker subgroups of patients with severe asthma. These findings support the role of TEZSPIRE as a first-in-class treatment for a broad population of people living with severe asthma, irrespective of biomarker levels. In the pooled analysis, TEZSPIRE, when added to standard of care, reduced asthma exacerbations in patients, irrespective of baseline blood eosinophil counts, demonstrating consistent efficacy with a 71%, 48% and 48% reduction in the AAER over 52 weeks, compared to placebo added to SoC. In the same analysis, TEZSPIRE also demonstrated improvements in AAER in patients regardless of fractional exhaled nitric oxide level and allergy status over 52 weeks, compared to placebo. Additionally, in a pre-specified exploratory analysis from NAVIGATOR, TEZSPIRE demonstrated consistent efficacy throughout the year regardless of season. Data show that TEZSPIRE reduced the AAER by 63%, 46%, 62% and 54% compared to placebo. The proportion of patients with an exacerbation was lower in the TEZSPIRE group than in the placebo group across all seasons.