Welcome to our dedicated page for Amgen news (Ticker: AMGN), a resource for investors and traders seeking the latest updates and insights on Amgen stock.
Amgen Inc. (AMGN) is a global biotechnology leader pioneering innovative therapies for serious illnesses. This dedicated news hub provides investors and healthcare professionals with essential updates on the company's latest developments, regulatory milestones, and strategic initiatives.
Track critical updates across Amgen's core therapeutic areas including oncology treatments, inflammatory disease therapies, and rare disease solutions. Our curated feed includes earnings reports, clinical trial data, partnership announcements, and manufacturing updates - all sourced directly from official channels.
Key resources include timely coverage of FDA decisions, research breakthroughs in biologics and biosimilars, and analysis of market-moving events. Bookmark this page for structured access to Amgen's evolving pipeline and business strategies without promotional bias.
Amgen (NASDAQ:AMGN) announced the presentation of important data from its cardiovascular portfolio at the American Heart Association Scientific Sessions 2020, scheduled for Nov. 13-17, 2020. Key highlights include new evidence supporting Repatha (evolocumab) for lowering cardiovascular events, the GOULD registry's findings on cholesterol treatment patterns, and initial data for olpasiran, an innovative siRNA targeting lipoprotein(a). Results from the GALACTIC-HF trial, which met its primary endpoint but missed its secondary one, will also be showcased, emphasizing Amgen's commitment to improving cardiovascular health.
Amgen (NASDAQ: AMGN) announced the first presentation of AMG 757 Phase 1 clinical data for relapsed or refractory small cell lung cancer (SCLC). The investigational bispecific T cell engager targets the DLL3 protein, overexpressed in SCLC. The interim analysis involved 40 patients, with 16% showing confirmed partial response and 29% with stable disease. Despite a 43% incidence of cytokine release syndrome (CRS), events were manageable. Results will be presented on Nov. 12 at the SITC 35th Annual Meeting, highlighting potential advancements in treating this aggressive cancer.
Amgen (NASDAQ:AMGN) will present at the 29th Annual Credit Suisse Virtual Healthcare Conference on Nov. 9, 2020, at 4:15 p.m. ET in Scottsdale, Ariz. Key executives, Murdo Gordon and Peter H. Griffith, will be representing the company. Investors can listen to the live audio on Amgen's website, with a replay available for 90 days. Founded in 1980, Amgen focuses on addressing unmet medical needs through innovative therapies and advanced human genetics. For more details, visit www.amgen.com.
Amgen reported Q3 2020 financial results with total revenues of $6.4 billion, up 12% year-over-year, driven by significant volume growth despite challenges due to COVID-19. Product sales also rose 12%, with notable increases in Otezla® and Repatha®. GAAP EPS increased 5% to $3.43, while non-GAAP EPS saw a 19% rise to $4.37. Free cash flow remained stable at $3.2 billion. Amgen narrowed its total revenue guidance for 2020 to $25.1-$25.5 billion and revised EPS guidance upwards.
Amgen (NASDAQ:AMGN) will release its third quarter financial results on October 28, 2020, after U.S. market close. Following this, a conference call will occur at 2:00 p.m. PT, featuring CEO Robert A. Bradway and senior management. The call will be accessible via live audio on Amgen's website, where it will also be archived for 90 days. Amgen continues to focus on innovative therapeutics, addressing high unmet medical needs, and has built a strong pipeline since its inception in 1980.
Amgen has completed discussions with the FDA regarding its Phase 2 trial for efavaleukin alfa, aimed at treating Systemic Lupus Erythematosus (SLE). This initiative is part of the FDA's Complex Innovative Trial Designs Pilot Program, focusing on modernizing drug development. The adaptive clinical trial design is expected to enhance the development of new therapies for SLE, addressing the significant unmet medical need in this area. The collaboration signals a commitment to improve efficiency and innovation in clinical trials.
Amgen (NASDAQ:AMGN) declared a $1.60 per share dividend for Q4 2020, payable on December 8, 2020, to shareholders recorded by November 16, 2020. This follows Amgen's commitment to improve health outcomes through innovative therapies, supported by a strong pipeline and advanced human genetics. The company, a pioneer in biotechnology since 1980, focuses on serious illnesses and has reached millions globally.
Amgen announced positive Phase 2 results for sotorasib, a KRAS G12C inhibitor, in treating advanced non-small cell lung cancer (NSCLC) in patients with prior treatment failures. The study involved 126 patients, showing an objective response rate consistent with past Phase 1 data and promising efficacy measures. More than half of responders remained on treatment at data cutoff. Amgen plans to discuss results with regulatory agencies and is advancing its development program, which includes a Phase 3 study, CodeBreaK 200, comparing sotorasib to docetaxel.
Amgen announced positive results for Aimovig (erenumab-aooe) at the Migraine Trust Virtual Symposium, showcasing a five-year study on its safety and efficacy in treating episodic migraine. The Phase 2 study involved 383 patients, with 216 completing the open-label phase. Results indicated a reduction of 5.3 monthly migraine days and 4.4 days less use of acute migraine medication. No increase in adverse events was recorded, affirming Aimovig's safety profile. This long-term data further establishes Aimovig as a leading preventive treatment for migraines.
Amgen announces updated data from the CodeBreaK 100 clinical study on sotorasib, a KRASG12C inhibitor, published in the New England Journal of Medicine. The study evaluated 129 patients across various advanced solid tumors. In 34 heavily pretreated patients with advanced non-small cell lung cancer (NSCLC), sotorasib showed an objective response rate of 35.3% and a disease control rate of 91.2%. Safety data demonstrated tolerability, with no dose-limiting toxicities. Upcoming Phase 2 results are highly anticipated among investors and the medical community.