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BAYER AG S/ADR (BAYRY) news covers developments at Bayer AG, a global life science enterprise active in health care and nutrition. Company communications highlight updates across its Pharmaceuticals Division, radiology business and crop science activities, giving investors and observers insight into how Bayer advances its pipeline and product portfolio.
Recent pharmaceutical news emphasizes growth in oncology, cardiology, neurology, immunology and women’s health. Examples include updates on asundexian for secondary stroke prevention, finerenone (Kerendia) in cardiovascular-kidney-metabolic conditions, and oncology assets such as Nubeqa for prostate cancer, Hyrnuo for HER2-mutant non-small cell lung cancer, and Xofigo for metastatic castration-resistant prostate cancer with bone metastases. Bayer also reports on Lynkuet, a hormone-free treatment for moderate to severe hot flashes due to menopause, and a Phase III SUNFLOWER study evaluating Mirena for nonatypical endometrial hyperplasia.
News items also describe Bayer’s work in radiology and molecular imaging, including the low-dose MRI contrast agent gadoquatrane and the acquisition of investigational tracers AT-01 and AT-05 for diagnosing cardiac amyloidosis. Additional coverage highlights cell and gene therapy programs for Parkinson’s disease and ophthalmic conditions, as well as collaborations such as the agreement with Soufflé Therapeutics to develop a heart-targeted siRNA therapy for a form of dilated cardiomyopathy.
On the agriculture side, Bayer Crop Science Canada announcements feature launches like Sivanto Energy for flea beetle control in canola and EverGol Rise for pulse disease control. Together, these updates illustrate how Bayer seeks to execute its mission “Health for all, Hunger for none” through pharmaceutical innovation, diagnostic imaging advances and crop protection solutions.
Bayer (OTC:BAYRY) announced FDA approval of Lynkuet (elinzanetant) 60 mg for moderate to severe hot flashes due to menopause on October 24, 2025. Lynkuet is described as the first dual NK1/NK3 receptor antagonist for this indication and is taken once daily at bedtime. Approval is supported by three Phase III trials (OASIS 1–3); OASIS 1 and 2 met co-primary endpoints at weeks 4 and 12 in 796 women, and safety was evaluated across 1,420 women with OASIS 3 including 627 participants up to 52 weeks. Lynkuet is expected to be available in the U.S. beginning November 2025.
Important safety notes include pregnancy risk, CNS daytime impairment, increased liver tests, and seizure risk.
Bayer (NASDAQ:BAYRY) announced late-breaking presentations of methods and baseline data from the global Phase III OCEANIC-STROKE study of investigational oral Factor XIa inhibitor asundexian 50 mg once daily at the 17th World Stroke Congress in Barcelona, October 22–24, 2025.
The multicenter, international, randomized, placebo-controlled, double-blind, event-driven trial enrolled >12,300 patients with non-cardioembolic ischemic stroke or high-risk TIA on standard antiplatelet therapy. Multiple sessions (plenary, free communication, and e-posters) will present study methods, baseline characteristics, sub-study participation factors, and real-world stroke burden analyses. Main study results will be presented at a future scientific congress. Asundexian remains an investigational agent and is not approved for any indication.
Bayer (NYSE:BAYRY) announced on October 7, 2025 that Cornfed Farms, a fourth-generation Mohr family operation, is the first Bayer ForwardFarm in the Midwest and the only ForwardFarm in the United States.
The designation joins Cornfed Farms with 15 other global ForwardFarms and highlights on-farm regenerative practices including no-till/minimum till, intermediate crops (CoverCress and camelina), diversified cash crops and livestock integration, and use of the Preceon Smart Corn System for data-driven insights and reduced synthetic nitrogen use.
One A Day (NASDAQ:BAYRY) announced a nationwide rebrand and new platform, “The ONE for you”, launching in fall 2025 to simplify multivitamin choice across age, gender, and life stages. The update includes a refreshed logo, brighter packaging, benefit icons (immune and bone health callouts), a new design system, and tagline lockups.
New packaging began appearing at major retailers including Walmart, Target, Walgreens, CVS, and Amazon in September 2025; a national media push and TV campaign also debuted that month, with full portfolio transition continuing into early 2026.
BlueRock Therapeutics (OTC:BAYRY) reported positive 36-month Phase I results for investigational cell therapy bemdaneprocel in Parkinson’s disease presented Oct 6, 2025. Safety at 36 months remained favorable with no adverse events related to therapy or surgery. F‑Dopa imaging suggests transplanted cells survive and engraft after stopping immunosuppression at 12 months. Motor outcomes showed clinically meaningful improvements versus baseline: MDS‑UPDRS Part III mean reductions of 17.9 points (high dose, n=7) and 13.5 points (low dose, n=4). High dose patients reported a +1 hour mean increase in “Good ON” time by PD Diary at 36 months. Participants continue in long‑term follow‑up and exPDite‑2 is planned to further evaluate benefits.
Bayer (OTC:BAYRY) has selected Interpublic Group (NYSE:IPG) as its global agency partner for creative, production, and media services for its Consumer Health division. The partnership will manage marketing activities for major brands including Aspirin, Bepanthen, Claritin, and Canesten.
The integrated agency approach aims to leverage GenAI tools and capabilities to enhance consumer engagement at the local level while maintaining global consistency. The new structure is designed to improve media buying power and deliver personalized content across markets. The partnership is set to go live on January 1, 2026, following a transition period.
Bayer (OTC:BAYRY) has announced a strategic distribution partnership with Mint Pharmaceuticals Inc. for ADALAT® XL® 30 mg tablets in Canada, effective September 3, 2025. The collaboration aims to enhance the accessibility of ADALAT® XL®, a medication indicated for chronic stable angina and mild to moderate essential hypertension management.
The partnership leverages Mint's 15-year experience in supply chain management and extensive distribution network in the Canadian market. ADALAT® XL®, which received its initial market authorization in Canada in 1995, will benefit from Mint's established infrastructure to ensure consistent availability to healthcare providers and patients across Canada.
Bayer (OTC:BAYRY) will present new data for KERENDIA® (finerenone) at the upcoming HFSA Annual Scientific Meeting in Minneapolis, September 26-29, 2025. The presentations will include two key subgroup analyses from the Phase III FINEARTS-HF trial examining treatment effects across heart failure duration and in patients with high medication burden.
The company will also present retrospective real-world data on guideline-directed medical therapy treatment patterns for newly diagnosed heart failure patients in the U.S. This follows the FDA's July 2025 approval of KERENDIA's new indication for treating adult patients with heart failure with left ventricular ejection fraction ≥40%. The drug was previously approved in July 2021 for reducing cardiovascular and kidney disease risks in adult patients with CKD associated with T2D.
Bayer (OTC:BAYRY) has announced significant progress in its dual approach to treating Parkinson's disease through both cell and gene therapies. The company has initiated two major clinical trials: the Phase III exPDite-2 trial for bemdaneprocel (cell therapy) and the Phase II REGENERATE-PD trial for AB-1005 (gene therapy).
The trials focus on treating moderate-stage Parkinson's disease, which affects over 10 million people globally. Bemdaneprocel aims to replace lost dopamine-producing cells, while AB-1005 explores gene therapy potential. The REGENERATE-PD trial is currently active in the UK, Poland, and USA, with Germany to follow.
These developments are being conducted through Bayer's subsidiaries, BlueRock Therapeutics LP and AskBio Inc., showcasing the company's comprehensive end-to-end approach in cell and gene therapy development.
Bayer (OTC:BAYRY) has announced the expansion of its "Take Care, Now" campaign in partnership with country star Luke Bryan and Feeding America®, marking their 10-year collaboration anniversary. The campaign addresses food insecurity and "hidden hunger" in rural America through multiple initiatives.
The campaign features a social media initiative #HeresToTheFarmer, where Bayer will donate up to 1 million meals through Feeding America for each hashtag share. The initiative includes food drives at Luke Bryan's Farm Tour 2025 locations, with stops in Wisconsin, Illinois, and Michigan.
Recent research reveals concerning trends: 90% of Americans have modified shopping habits due to rising food prices, with rural families experiencing a 12-point decline in food quality compared to urban areas. To date, Bayer has provided over 10 million meals through the campaign and helped 3.4 million mothers and babies through their partnership with Vitamin Angels.
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