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Bristol Myers Squibb’s Investigational LPA1 Antagonist Reduces the Rate of Lung Function Decline in Patients with Idiopathic Pulmonary Fibrosis
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Bristol Myers Squibb to Highlight Diversified Approaches and Commitment to Improving Outcomes for Patients with Cancer and Serious Blood Disorders at ASCO, EHA and ICML 2023
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Bristol Myers Squibb Receives European Commission Approval for CAR T Cell Therapy Breyanzi (lisocabtagene maraleucel) for Relapsed or Refractory Large B-cell Lymphoma After One Prior Therapy
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Bristol Myers Squibb to Participate in Bank of America Securities 2023 Healthcare Conference
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Bristol-Myers Squibb (BMY) Announces FDA Priority Review of BLA and EMA Validation of Reblozyl
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U.S. FDA Accepts for Priority Review Supplemental Biologics License Application and EMA Validates Application for Reblozyl® (luspatercept-aamt) as First-Line Treatment of Anemia in Adults with Lower-
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Immatics Announces First Bristol Myers Squibb Opt-in of TCR-T Candidate from Ongoing Multi-target Strategic Collaboration
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Immatics Announces First Bristol Myers Squibb Opt-in of TCR-T Candidate from Ongoing Multi-target Strategic Collaboration
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Bristol-Myers Squibb's (BMY) TRANSCEND FL and TRANSCEND NHL 001 Studies of Breyanzi Meet Primary Endpoint of Overall Response Rate
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Bristol Myers Squibb’s TRANSCEND FL and TRANSCEND NHL 001 Studies of Breyanzi (lisocabtagene maraleucel) in Relapsed or Refractory Follicular Lymphoma and Mantle Cell Lymphoma Meet Primary Endpoint
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Bristol Myers Squibb Reports First Quarter Financial Results for 2023
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Bristol-Myers Squibb (BMY) Announces Leadership Transition
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Bristol Myers Squibb Announces Leadership Transition Plan
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Bristol-Myers Squibb (BMY) Receives Positive CHMP Opinion Recommending Approval for CAMZYOS (mavacamten) for the Treatment of Symptomatic Obstructive Hypertrophic Cardiomyopathy
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Bristol Myers Squibb Receives Positive CHMP Opinion Recommending Approval for CAMZYOS® (mavacamten) for the Treatment of Symptomatic Obstructive Hypertrophic Cardiomyopathy (HCM)
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Bristol-Myers Squibb (BMY) Announces New U.S. Manufacturing Facility for Viral Vector Production
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Bristol Myers Squibb Strengthens Cell Therapy Capabilities by Adding New U.S. Manufacturing Facility for Viral Vector Production
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Bristol-Myers Squibb (BMY) and Tubulis Enter License Agreement to Develop Next Generation ADCs for the Treatment of Cancer Patients
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Tubulis Announces Strategic License Agreement with Bristol Myers Squibb to Develop Next Generation ADCs for the Treatment of Cancer Patients
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Bristol-Myers (BMY), 2seventy (TSVT) Announces Regulatory Applications Accepted Across Three Regions Globally for Abecma for Earlier Use in Adults with Triple-Class Exposed R/R Multiple Myeloma
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Regulatory Applications Accepted Across Three Regions Globally for Abecma for Earlier Use in Adults with Triple-Class Exposed Relapsed and/or Refractory Multiple Myeloma
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Foundation Medicine and Bristol Myers Squibb Expand Partnership to Focus on Companion Diagnostic Development
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Bristol-Myers Squibb (BMY) Receives Positive CHMP Opinion for CAR T Cell Therapy Breyanzi for Relapsed or Refractory Large B-cell Lymphoma After One Prior Therapy
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Bristol Myers Squibb Receives Positive CHMP Opinion for CAR T Cell Therapy Breyanzi (lisocabtagene maraleucel) for Relapsed or Refractory Large B-cell Lymphoma After One Prior Therapy
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Bristol-Myers Squibb (BMY) Announces Neoadjuvant Opdivo with Chemotherapy Demonstrates Long-Term, Durable Clinical Benefits for Patients with Resectable NSCLC at Three Years in the CheckMate -816 Tria
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Neoadjuvant Opdivo (nivolumab) with Chemotherapy Demonstrates Long-Term, Durable Clinical Benefits for Patients with Resectable Non-Small Cell Lung Cancer at Three Years in the CheckMate -816 Trial
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Bristol-Myers Squibb (BMY) Receives European Commission Approval of Sotyktu, a Once-Daily Oral Treatment for Adults With Moderate-to-Severe Plaque Psoriasis
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Bristol Myers Squibb Receives European Commission Approval of Sotyktu (deucravacitinib), a Once-Daily Oral Treatment for Adults With Moderate-to-Severe Plaque Psoriasis
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Evotec and Bristol Myers Squibb Extend and Expand Strategic Neurodegeneration Partnership
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Bristol Myers Squibb Announces Progress Toward Long-Term Inclusion & Diversity Goals and Health Equity Commitments
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Bristol Myers Squibb to Report Results for First Quarter 2023 on April 27, 2023
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Bristol Myers Squibb Announces Dividend
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Bristol-Myers Squibb (BMY) Granted EU Approval of Reblozyl for Anemia in Adult Patients with Non-Transfusion-Dependent Beta Thalassemia
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Bristol Myers Squibb Receives European Commission Approval of Reblozyl® (luspatercept) for Anemia in Adult Patients with Non-Transfusion-Dependent Beta Thalassemia
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The Bristol Myers Squibb-Janssen Collaboration Launches Pivotal Phase 3 Librexia Clinical Trial Program Evaluating Milvexian, an Investigational Oral Factor XIa Inhibitor
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Bristol-Myers Squibb (BMY) Announces FDA Accepts Supplemental Biologics License Application and European Medicines Agency Validates Application for Opdivo
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U.S. Food and Drug Administration Accepts Bristol Myers Squibb’s Supplemental Biologics License Application and European Medicines Agency Validates Application for Opdivo (nivolumab) ….
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Bristol Myers Squibb to Participate in Cowen’s 43rd Annual Health Care Conference
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Bristol Myers Squibb to Present Data Supporting its Cardiovascular Portfolio at the American College of Cardiology Annual Scientific Session Together With World Congress of Cardiology
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Bristol-Myers Squibb (BMY) Reports Strong Adjuvant Opdivo Data from CheckMate -274 Trial
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Adjuvant Opdivo (nivolumab) Continues to Provide Significant, Durable Clinical Benefits for Patients with Radically Resected, High-Risk Muscle-Invasive Urothelial Carcinoma After Three Years in CheckM
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Basketball Legend Kareem Abdul-Jabbar Joins No Time to Wait Campaign to Raise Awareness of Atrial Fibrillation (AFib) and its Symptoms
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Exelixis (EXEL) and Bristol Myers Squibb (BMY) Reports Strong Results from Phase 3 CheckMate-9ER Trial
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Opdivo® (nivolumab) in Combination with CABOMETYX® (cabozantinib) Shows Durable Survival with Over Three Years of Follow-Up in the CheckMate -9ER Trial in First-Line Advanced Renal Cell Carcinoma
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Bristol-Myers (BMY), 2seventy (TSVT) Announces Abecma Reduced Risk of Disease Progression, Death by 51% Versus Standard Regimens in Earlier Lines of Therapy for R/R Multiple Myeloma Based on Results f
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Abecma (idecabtagene vicleucel) Reduced the Risk of Disease Progression or Death by 51% Versus Standard Regimens in Earlier Lines of Therapy for Relapsed and Refractory Multiple Myeloma Based on Resul
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Bristol Myers Squibb to Participate in the Guggenheim Healthcare Talks 2023 Oncology Conference
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Bristol Myers Squibb Reports Fourth Quarter and Full-Year Financial Results for 2022
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Bristol-Myers Squibb (BMY) Receives Positive CHMP Opinion for Reblozyl for Adult Patients with Anemia-Associated, NTD Beta Thalassemia
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Bristol Myers Squibb Receives Positive CHMP Opinion for Reblozyl® (luspatercept) for Adult Patients with Anemia-Associated, Non-Transfusion-Dependent (NTD) Beta Thalassemia

