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Bristol Myers Squibb’s Investigational LPA1 Antagonist Reduces Rate of Lung Function Decline in Progressive Pulmonary Fibrosis Cohort of Phase 2 Study
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Bristol Myers Squibb Celebrates a Decade of Its Coast 2 Coast 4 Cancer Cross-Country Bike Ride in Support of the V Foundation for Cancer Research
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Bristol Myers Squibb to Participate in the Morgan Stanley 21st Annual Global Healthcare Conference
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Bristol-Myers Squibb (BMY) Announces FDA Approval of Reblozyl for Anemia in Adults with Lower-Risk Myelodysplastic Syndromes (MDS) Who May Require Transfusions
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U.S. FDA Approves Bristol Myers Squibb’s Reblozyl® (luspatercept-aamt) as First-Line Treatment of Anemia in Adults with Lower-Risk Myelodysplastic Syndromes (MDS) Who May Require Transfusions
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Bristol-Myers Squibb (BMY) Reports Follow-Up Data from Two Phase 3 Studies of CAMZYOS Demonstrate Consistent and Durable Response
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Long-Term Follow-Up Data from Two Phase 3 Studies of CAMZYOS® (mavacamten) Demonstrate Consistent and Durable Response in Patients with Symptomatic Obstructive Hypertrophic Cardiomyopathy (HCM)
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Retrospective Observational Study Assessing Real-World Clinical Impact of Switching or Continuing Eliquis® or Rivaroxaban Presented at the European Society of Cardiology (ESC) Congress 2023
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Bristol Myers Squibb Shares Progress Toward Its Environmental, Social, and Governance Initiatives and Its Health Equity Commitments
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Bristol-Myers Squibb (BMY) Receives European Commission Approval for Opdivo as an Adjuvant Treatment for Patients with Completely Resected Stage IIB or IIC Melanoma
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Bristol Myers Squibb Receives European Commission Approval for Opdivo (nivolumab) as an Adjuvant Treatment for Patients with Completely Resected Stage IIB or IIC Melanoma
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Bristol Myers Squibb to Showcase Data Across its Innovative Cardiovascular Portfolio at the European Society of Cardiology Congress 2023
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Bristol-Myers Squibb (BMY) Updated Data from TRIDENT-1 Trial Show Durable Efficacy Benefits with Repotrectinib for Patients with Locally Advanced or Metastatic ROS1-Positive NSCLC
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Updated Data from TRIDENT-1 Trial Show Durable Efficacy Benefits with Repotrectinib for Patients with Locally Advanced or Metastatic ROS1-Positive Non-Small Cell Lung Cancer
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Bristol Myers Squibb Inducted into the Billion Dollar Roundtable, Expands Supplier Diversity Efforts
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Bristol-Myers Squibb (BMY) Enters Into $4 Billion Aggregate Accelerated Share Repurchase Agreements
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Bristol Myers Squibb Enters Into $4 Billion Aggregate Accelerated Share Repurchase Agreements
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Bristol Myers Squibb Launches Clear Understanding Campaign to Reveal the Plain Truth About Living with Moderate to Severe Plaque Psoriasis
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Bristol Myers Squibb Reports Second Quarter Financial Results for 2023
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Immatics (IMTX) Announces $35 Million Equity Investment from Bristol Myers Squibb (BMY)
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Immatics Announces $35 Million Equity Investment from Bristol Myers Squibb
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Bristol-Myers Squibb (BMY) Reports Positive CHMP Opinion Recommending Approval for Opdivo as Adjuvant Treatment
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Bristol Myers Squibb Receives Positive CHMP Opinion Recommending Approval for Opdivo (nivolumab) as an Adjuvant Treatment for Patients with Completely Resected Stage IIB or IIC Melanoma
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Bristol Myers Squibb Launches Supporting You with UC, with Women’s World Cup Commentator, Former Professional Soccer Player and Ulcerative Colitis Patient, Rosie White
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Bristol-Myers Squibb (BMY) Reports Opdivo with Cisplatin-Based Chemotherapy Shows Overall Survival and Progression-Free Survival Benefit for Cisplatin-Eligible Patients with Unresectable or Metastatic
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Opdivo (nivolumab) in Combination with Cisplatin-Based Chemotherapy Shows Overall Survival and Progression-Free Survival Benefit for Cisplatin-Eligible Patients with Unresectable or Metastatic Urothel
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Evotec and Bristol Myers Squibb Enter Licence Agreement within Neuroscience Partnership
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Bristol-Myers Squibb (BMY) Granted EU Approval for Opdivo with Chemotherapy as Neoadjuvant Treatment
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Bristol Myers Squibb Receives European Commission Approval for Opdivo (nivolumab) with Chemotherapy as Neoadjuvant Treatment of Resectable Non-Small Cell Lung Cancer at High Risk of Recurrence in Pati
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Bristol-Myers Squibb (BMY) Receives European Commission Approval of CAMZYOS (mavacamten), for the Treatment of Symptomatic Obstructive Hypertrophic Cardiomyopathy
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Bristol Myers Squibb Receives European Commission Approval of CAMZYOS® (mavacamten), for the Treatment of Symptomatic Obstructive Hypertrophic Cardiomyopathy (HCM)
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Bristol Myers Squibb’s Breyanzi (lisocabtagene maraleucel) Delivers Deep and Durable Responses in Relapsed or Refractory Follicular Lymphoma and Mantle Cell Lymphoma in TRANSCEND Clinical Trials Pre
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Bristol-Myers Squibb (BMY) Announces FDA Approval of Addition of Positive Data from Phase 3 VALOR-HCM Study to CAMZYOS Label
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U.S. Food and Drug Administration Approves Addition of Positive Data from Phase 3 VALOR-HCM Study to CAMZYOS® (mavacamten) Label
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Bristol Myers Squibb Announces Dividend
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Bristol-Myers Squibb (BMY) Receives FDA Approval of New Cell Therapy Manufacturing Facility in Devens, Massachusetts
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Bristol Myers Squibb Receives U.S. FDA Approval of New State-of-the-Art Cell Therapy Manufacturing Facility in Devens, Massachusetts
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Bristol Myers Squibb to Report Results for Second Quarter 2023 on July 27, 2023
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Four-Year Outcomes from Phase 3 CheckMate -9LA Trial Show Durable, Long-Term Survival with Opdivo (nivolumab) Plus Yervoy (ipilimumab) with Two Cycles of Chemotherapy for Patients with Metastatic Non-
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Bristol Myers Squibb to Participate in Upcoming Investor Conferences
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Bristol Myers Squibb to Hold R&D Day on September 14
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Bristol Myers Squibb to Present Late-Breaking Data for Breyanzi (lisocabtagene maraleucel) in Relapsed or Refractory Follicular Lymphoma and Mantle Cell Lymphoma at 2023 International Conference on Ma
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Bristol-Myers Squibb (BMY) Announces FDA Accepts for Priority Review Application for Repotrectinib for the Treatment of Patients with Locally Advanced or Metastatic ROS1-Positive NSCLC
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U.S. Food and Drug Administration Accepts for Priority Review Bristol Myers Squibb’s Application for Repotrectinib for the Treatment of Patients with Locally Advanced or Metastatic ROS1-Positive Non
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Bristol-Myers Squibb (BMY) Receives Positive CHMP Opinion Recommending Approval for Opdivo with Chemotherapy
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Bristol Myers Squibb Receives Positive CHMP Opinion Recommending Approval for Opdivo (nivolumab) with Chemotherapy as Neoadjuvant Treatment of Resectable Non-Small Cell Lung Cancer at High Risk of Rec
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Bristol Myers Squibb’s Breyanzi (lisocabtagene maraleucel) is First and Only CAR T to Deliver Deep and Durable Efficacy in Pivotal Multicenter Trial in Relapsed or Refractory Chronic Lymphocytic Leu
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Bristol-Myers Squibb (BMY) to Present First Results at ASCO and EHA from Phase 3 COMMANDS Study of Reblozyl
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Bristol Myers Squibb to Present First Results at ASCO and EHA from Phase 3 COMMANDS Study of Reblozyl® (luspatercept-aamt) in First-Line Treatment of Anemia in Adults with Lower-Risk Myelodysplastic
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Bristol-Myers Squibb's (BMY) Investigational LPA1 Antagonist Reduces the Rate of Lung Function Decline in Patients with Idiopathic Pulmonary Fibrosis

