BMY
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News25/Ratings12
News · 26 weeks119-44%
2025-10-262026-04-19
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Latest news
25 items- PRAtrium Therapeutics Earns $15 Million Milestone Payment from Bristol Myers Squibb Under Global Cardiovascular CollaborationSAN DIEGO, April 23, 2026 /PRNewswire/ -- Atrium Therapeutics, Inc. (NASDAQ:RNA) (the "Company"), a biopharmaceutical company dedicated to delivering RNA therapeutics directly to the heart, announced today it has earned a $15 million development milestone payment from Bristol Myers Squibb (NYSE:BMY). The milestone was achieved upon the successful delivery of a development candidate for the first licensed compound targeting a cardiology indication under the Company's ongoing collaboration. "This milestone marks a meaningful step forward for Atrium, further expanding our RNA deliv
- PRFoundation Medicine Expands Existing Collaboration with Bristol Myers Squibb to Develop a Next-Generation Sequencing Companion Diagnostic to Identify Patients with Homozygous MTAP DeletionFoundation Medicine, Inc., a global precision medicine company, today announced an expansion to its collaboration with Bristol Myers Squibb (NYSE:BMY) to develop FoundationOne®CDx as a next-generation sequencing-based companion diagnostic to identify patients with homozygous MTAP deletion in multiple indications for an investigational targeted therapy. The expansion broadens Foundation Medicine's longstanding relationship in advancing biomarker-driven therapies with Bristol Myers Squibb. Homozygous deletion is a major cause of MTAP deficiency.1 Copy number calling can have low signal-to-noise ratio, making the alterations challenging to accurately identify. FoundationOne CDx is a tissue-b
- PRArdelyx Appoints Biopharmaceutical Veteran, Felecia W. Ettenberg, as Chief Legal OfficerWALTHAM, Mass., April 20, 2026 (GLOBE NEWSWIRE) -- Ardelyx, Inc. (NASDAQ:ARDX), a biopharmaceutical company focused on the development and commercialization of innovative medicines that meet significant unmet medical needs, today announced the appointment of Felecia W. Ettenberg, a seasoned leader with more than 25 years of legal experience in the biopharmaceutical industry, as Chief Legal Officer (CLO). She will oversee Ardelyx's legal, compliance, regulatory, and government affairs operations. Ms. Ettenberg succeeds Elizabeth Grammer, who has chosen to retire after an extraordinary 16-year career at the company. "I am thrilled to welcome Felecia as our new Chief Legal Officer," said Mik
- SECSEC Form DEFA14A filed by Bristol-Myers Squibb CompanyDEFA14A - BRISTOL MYERS SQUIBB CO (0000014272) (Filer)
- PRBeeline Medicines Debuts to Deliver Category-Leading Precision Therapies for People Living with Autoimmune and Inflammatory Diseases– Advancing a broad portfolio designed to deliver multiple paradigm-shifting therapies for devastating and underserved immune-mediated diseases – – Lead program afimetoran, a potential best-in-disease oral therapy for lupus, to complete Phase 2 trial in 2H 2026 before commencing pivotal development program – – Saqib Islam, Chief Executive Officer, leads established executive team with proven track record in drug development and global commercialization of first- and best-in-class medicines – – $300 million Series A financing led by Bain Capital supports operations into late-stage clinical development – STAMFORD, Conn. and BOSTON, April 15, 2026 (GLOBE NEWSWIRE) -- Beeline Medicines
- PROxford BioTherapeutics Enters Strategic Collaboration with Bristol Myers Squibb to Discover and Develop Next-Generation T-cell Engagers for Solid TumoursCollaboration leverages OBT's proprietary OGAP®-Verify discovery platform and drug development capabilities in alignment with BMS's expertise to advance selected novel oncology targets This is OBT's third major pharma collaboration within the past 12 months and reflects strong validation of the OGAP®-Verify platform's potential to drive oncology innovationOBT to receive an upfront payment and may be eligible to receive milestone payments, as well as royalties on net sales Oxford, UK and San Jose, California, 9 April 2026 – Oxford BioTherapeutics ("OBT"), is a clinical stage oncology company focused on the discovery and development of immuno-oncology (IO) and Antibody Drug Conjugate (ADC)-b
- INSIDERSEC Form 4 filed by Shanahan Karin4 - BRISTOL MYERS SQUIBB CO (0000014272) (Issuer)
- INSIDERSEC Form 4 filed by Elkins David V4 - BRISTOL MYERS SQUIBB CO (0000014272) (Issuer)
- INSIDERSEC Form 4 filed by Yale Phyllis R4 - BRISTOL MYERS SQUIBB CO (0000014272) (Issuer)
- INSIDERSEC Form 4 filed by Samuels Theodore R. Ii4 - BRISTOL MYERS SQUIBB CO (0000014272) (Issuer)
- INSIDERSEC Form 4 filed by Rice Derica W4 - BRISTOL MYERS SQUIBB CO (0000014272) (Issuer)
- INSIDERSEC Form 4 filed by Mcmullen Michael R.4 - BRISTOL MYERS SQUIBB CO (0000014272) (Issuer)
- INSIDERSEC Form 4 filed by Arduini Peter J4 - BRISTOL MYERS SQUIBB CO (0000014272) (Issuer)
- PRBristol Myers Squibb Evolves and Expands Standing in the Gaap to Advance More Equitable Care in Multiple Myeloma as Program Marks Ten YearsNew survey, guided by patient advocacy input, seeks to elevate lived experience and community voice to better understand challenges in multiple myeloma care Bristol Myers Squibb (NYSE:BMY), a global leader in oncology, today announced the evolution of Standing in the Gaap, a long-running program designed to help address persistent gaps in care for people living with multiple myeloma (MM) in medically underserved communities. Building on a decade of sustained commitment, BMS is reinforcing its focus on equitable access to multiple myeloma education, resources, and community-driven solutions by expanding the program to reach more patients and care partners. As a central element of the Sta
- PRBristol Myers Squibb Presents Positive Results from Phase 3 SCOUT-HCM Trial Demonstrating Efficacy and Safety of Camzyos (mavacamten) in Adolescents with Symptomatic Obstructive Hypertrophic Cardiomyopathy (oHCM)Trial met its primary endpoint, demonstrating clinically meaningful and statistically significant reduction in Valsalva left ventricular outflow tract (LVOT) gradient at Week 28 Results demonstrate the potential for Camzyos to be the first targeted pharmacological therapy for the treatment of oHCM in adolescents Safety profile of Camzyos in adolescents was similar to established profile in adults, with no new safety signals and no patients experiencing left ventricular ejection fraction (LVEF) of <50% Bristol Myers Squibb (NYSE:BMY) today announced positive data from the Phase 3 SCOUT-HCM trial of Camzyos (mavacamten), the first study of a cardiac myosin inhibitor (CMI) in adolescents
- PROpen Label Outpatient Switch Study Demonstrates Symptom Stability During Transition from Oral Atypical Antipsychotics to Cobenfy™ (xanomeline and trospium chloride)High treatment completion and no discontinuations due to lack of efficacy observed across faster and slower switch strategies Bristol Myers Squibb (NYSE:BMY) today announced data from a Phase 4 clinical trial evaluating the symptom stability, safety and tolerability of Cobenfy (xanomeline and trospium chloride) when switching adult outpatients with schizophrenia from an oral atypical antipsychotic to Cobenfy monotherapy. Through 8 weeks, patients remained stable with mean Positive and Negative Syndrome Scale (PANSS) total scores remaining below baseline, and no new safety signals were observed, regardless of cross-titration duration. These findings provide important evidence to help infor
- SECSEC Form 15-12G filed by Bristol-Myers Squibb Company15-12G - BRISTOL MYERS SQUIBB CO (0000014272) (Filer)
- SECSEC Form DEFA14A filed by Bristol-Myers Squibb CompanyDEFA14A - BRISTOL MYERS SQUIBB CO (0000014272) (Filer)
- SECSEC Form DEF 14A filed by Bristol-Myers Squibb CompanyDEF 14A - BRISTOL MYERS SQUIBB CO (0000014272) (Filer)
- PRThree New Studies Show Viz.ai's Cardio Suite Speeds Detection of Cardiac Disease and Improves Patient Follow-UpReal-world evidence to be presented at the American College of Cardiology Scientific Session 2026 highlights impact of Viz HCM, developed as part of a multi-year agreement with Bristol Myers Squibb, on disease detection and increasing access to life-saving treatments Viz.ai, the leader in AI-powered disease detection and intelligent care coordination, today announced that three abstracts featuring Viz HCM, the company's AI-powered ECG analysis and care coordination solution designed to detect and triage patients with signs of hypertrophic cardiomyopathy (HCM), part of the Viz Cardio Suite, have been accepted for presentation at the American College of Cardiology's Annual Scientific Sessio
- PRinsitro and Bristol Myers Squibb Collaboration Expanded with Nomination of New TargetsCollaboration expands to include two additional therapeutic targets for the treatment of ALS discovered via insitro's AI-driven Virtual Human™ platform Joint effort focuses on identifying key biological drivers to deliver disease-modifying interventions for ALS patients insitro, the AI therapeutics company built on causal biology, today announced the expansion of its strategic collaboration with Bristol Myers Squibb (NYSE:BMY) to advance a broadened portfolio of therapeutic programs for amyotrophic lateral sclerosis (ALS). The collaboration is focused on accelerating and delivering disease-modifying interventions designed to address the underlying biological drivers of ALS. BMS has no
- PRBristol Myers Squibb Reinforces Leadership in oHCM with New Camzyos (mavacamten) Data at American College of Cardiology Annual Scientific Session & Expo 2026 (ACC.26)Positive Phase 3 results of SCOUT-HCM trial highlight potential of Camzyos to be the first cardiac myosin inhibitor for the treatment of adolescents with symptomatic obstructive hypertrophic cardiomyopathy (oHCM) New real-world evidence further reinforces the long-term, consistent efficacy and safety profile of Camzyos across diverse patient populations in oHCM Bristol Myers Squibb (NYSE:BMY) today announced the presentation of new clinical trial and real-world data for Camzyos (mavacamten) at the American College of Cardiology's (ACC) Annual Scientific Session & Expo, taking place March 28–30, 2026, in New Orleans, Louisiana. Presentations at ACC will build upon the most comprehensive
- PRBristol Myers Squibb Transforms the Classical Hodgkin Lymphoma Treatment Paradigm with Expanded U.S. and EMA Approvals for Opdivo® (nivolumab)In the U.S., FDA approval establishes Opdivo in combination with doxorubicin, vinblastine and dacarbazine (AVD) as the first immunotherapy combination approved for adult and pediatric patients 12 years and older with previously untreated, Stage III or IV classical Hodgkin Lymphoma (cHL) With approval in the EU, Opdivo in combination with brentuximab vedotin is now the first immunotherapy combination approved to treat certain pediatric and adult patients with relapsed or refractory cHL Bristol Myers Squibb (NYSE:BMY) today announced that Opdivo® (nivolumab) has received approval for two new classical Hodgkin Lymphoma (cHL) indications in the U.S. and the European Union (EU). The U.S. Foo
- PRBristol Myers Squibb to Report Results for First Quarter 2026 on April 30, 2026Bristol Myers Squibb (NYSE:BMY) will announce results for the first quarter of 2026 on Thursday, April 30, 2026. Company executives will review financial results with the investment community during a conference call beginning at 8:00 a.m. ET. Investors and the general public are invited to listen to a live audio webcast of the call at http://investor.bms.com. Materials related to the call will be available on the company's Investor Relations website prior to the start of the conference call. A replay of the webcast will be available here approximately three hours after the conference call concludes. About Bristol Myers Squibb: Transforming Patients' Lives Through Science At Bristol
- INSIDERSEC Form 4 filed by President, RayzeBio Org. Hickey Benjamin4 - BRISTOL MYERS SQUIBB CO (0000014272) (Issuer)