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Bristol Myers Squibb Announces Positive Topline Results from Phase 3 VALOR-HCM Trial, Evaluating Mavacamten in Patients with Obstructive Hypertrophic Cardiomyopathy Who are Eligible for Septal Reducti
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Bristol-Myers Squibb (BMY) Prices $6B Worth of Senior Unsecured Notes
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Bristol Myers Squibb Prices $6 Billion of Senior Unsecured Notes
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Bristol-Myers Squibb (BMY) Announces Tender Offers for an Aggregate Purchase Price of Up to $4B
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Bristol Myers Squibb Announces Tender Offers for an Aggregate Purchase Price of Up to $4.0 Billion
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Bristol-Myers Squibb (BMY) and Exelisis (EXEL) Report that Opdivo in Combination with CABOMETYX Demonstrates Continued Survival Benefits with Over Two Years of Follow-Up in the CheckMate -9ER Trial
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Opdivo® (nivolumab) in Combination with CABOMETYX® (cabozantinib) Demonstrates Continued Survival Benefits with Over Two Years of Follow-Up in the CheckMate -9ER Trial in First-Line Advanced Renal C
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Bristol-Myers Squibb (BMY) Announces $5 Billion Aggregate Accelerated Share Repurchase Agreements
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Bristol Myers Squibb Enters Into $5 Billion Aggregate Accelerated Share Repurchase Agreements
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Bristol Myers Squibb Awards Nearly $8 Million in New Health Equity Grants to Improve Access to Care for Medically Underserved Patients in U.S.
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Bristol Myers Squibb Reports Fourth Quarter and Full-Year Financial Results for 2021
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Bristol-Myers Squibb (BMY) Receives Positive CHMP Opinion for CAR T Cell Therapy Breyanzi for R/R DLBCL, PMBCL and FL3B
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Bristol Myers Squibb Receives Positive CHMP Opinion for CAR T Cell Therapy Breyanzi (lisocabtagene maraleucel) for Relapsed or Refractory DLBCL, PMBCL and FL3B
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Evotec Expands Neuroscience Collaboration with Bristol Myers Squibb to Include New Targeted Protein Degradation Approach
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Evotec Expands Neuroscience Collaboration with Bristol Myers Squibb to Include New Targeted Protein Degradation Approach
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ArsenalBio Announces Expansion of Collaboration with Bristol Myers Squibb to Advance T Cell Therapy in Solid Tumors
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Century Therapeutics (IPSC) and Bristol Myers Squibb (BMY) Announce Strategic Collaboration to Develop iPSC-derived Allogeneic Cell Therapies
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Century Therapeutics and Bristol Myers Squibb Enter into a Strategic Collaboration to Develop iPSC-derived Allogeneic Cell Therapies
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Century Therapeutics and Bristol Myers Squibb Enter into a Strategic Collaboration to Develop iPSC-derived Allogeneic Cell Therapies
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Bristol-Myers Squibb (BMY) Provides 2022 Total Revenue and Non-GAAP EPS Guidance, Announces $5 Billion Accelerated Share Repurchase
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Bristol Myers Squibb to Highlight Long-Term Growth Strategy at J.P. Morgan’s 40th Annual Healthcare Conference
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Bristol Myers Squibb Selects ZS To Support Global Commercialization and Analytics Capabilities
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Bristol Myers Squibb to Present at J.P. Morgan’s 40th Annual Healthcare Conference
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Bristol Myers Squibb to Report Results for Fourth Quarter 2021 on February 4, 2022
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U.S. Food and Drug Administration Approves Orencia® (abatacept) in Combination with a Calcineurin Inhibitor and Methotrexate for the Prevention of Acute Graft Versus Host Disease (aGvHD)...
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Exelixis Announces Initiation of Phase 1b Trial Evaluating XL092 in Combination with Immuno-oncology Therapies in Patients with Advanced Solid Tumors
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Immatics (IMTX), Bristol Myers Squibb (BMY) Enter Into Global Exclusive License for Immatics’ TCR Bispecific Program IMA401
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Immatics and Bristol Myers Squibb Enter Into Global Exclusive License for Immatics’ TCR Bispecific Program IMA401
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Immatics and Bristol Myers Squibb Enter Into Global Exclusive License for Immatics’ TCR Bispecific Program IMA401
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Bristol-Myers Squibb (BMY) Announces Dividend Increase, Additional $15 Billion Share Repurchase
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Bristol Myers Squibb Announces Dividend Increase and Additional $15 Billion Share Repurchase Authorization
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Bristol-Myers Squibb's (BMY) Breyanzi Significantly Improves Outcomes, Showing Superiority Over 20-Year Standard of Care in Second-Line Relapsed or Refractory Large B-cell Lymphoma Based on TRANSFORM
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Bristol Myers Squibb’s Breyanzi (lisocabtagene maraleucel) Significantly Improves Outcomes, Showing Superiority Over 20-Year Standard of Care in Second-Line Relapsed or Refractory Large B-cell Lymph
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Bristol-Myers Squibb (BMY) Granted FDA Priority Review for BLA for Reblozyl
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U.S. Food and Drug Administration Accepts for Priority Review supplemental Biologics License Application for Reblozyl® (luspatercept-aamt) in Adults with Non-Transfusion Dependent (NTD) Beta Thalasse
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Bristol-Myers Squibb (BMY) Applications for Deucravacitinib for Treatment of Moderate to Severe Plaque Psoriasis Accepted by FDA and Validated by EMA
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Bristol Myers Squibb’s Applications for Deucravacitinib for the Treatment of Moderate to Severe Plaque Psoriasis Accepted by U.S. Food and Drug Administration and Validated by European Medicines Age
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Bristol-Myers Squibb (BMY) Receives European Commission Approval of Zeposia for use in Adults with Moderately to Severely Active UC
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Bristol Myers Squibb Receives European Commission Approval of Zeposia (ozanimod) for use in Adults with Moderately to Severely Active Ulcerative Colitis
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Bristol-Myers Squibb (BMY) Announces New April PDUFA Date for Mavacamten
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Bristol Myers Squibb Announces New PDUFA Date for Mavacamten
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Bristol Myers Squibb Awards “Golden Tickets” to Promising Biotechs for Residencies at LabCentral, Biolabs@NYULangone and MBC BioLabs
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Bristol-Myers Squibb (BMY) Announces Late-Breaking Phase 2 Data for Investigational Oral Factor XIa Inhibitor Milvexian Suggest Favorable Antithrombotic Profile Across a Wide Range of Doses
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Late-Breaking Phase 2 Data for Investigational Oral Factor XIa Inhibitor Milvexian Suggest Favorable Antithrombotic Profile Across a Wide Range of Doses
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Bristol Myers Squibb Launches Could It Be HCM? Campaign to Increase Awareness of Hypertrophic Cardiomyopathy (HCM), the Most Common Inherited Heart Disease
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Bristol Myers Squibb to Take Part in Wolfe Research Virtual Healthcare Conference
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Evotec Reaches Programme Designations in Neuroscience Collaboration with Bristol Myers Squibb
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Bristol-Myers Squibb (BMY) Announces Neoadjuvant Opdivo Plus Chemotherapy Significantly Improves EFS in Patients with Resectable Non-Small Cell Lung Cancer in Phase 3 CheckMate -816 Trial
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Neoadjuvant Opdivo (nivolumab) Plus Chemotherapy Significantly Improves Event-Free Survival in Patients with Resectable Non-Small Cell Lung Cancer in Phase 3 CheckMate -816 Trial
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Bristol Myers Squibb to Present Data Across Robust Cardiovascular Portfolio at American Heart Association Scientific Sessions 2021

