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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 and The Rockefeller University Announce License Agreement for SARS-CoV-2 Neutralizing Monoclonal Antibody Combination for the Treatment of COVID-19
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Bristol-Myers Squibb (BMY) Announces Positive Topline Results from Second Pivotal Phase 3 Psoriasis Study Showing Superiority of Deucravacitinib Compared to Placebo and Otezla
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WuXi STA to Purchase Bristol Myers Squibb Manufacturing Facility in Couvet, Switzerland
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Bristol Myers Squibb Announces Positive Topline Results from Second Pivotal Phase 3 Psoriasis Study Showing Superiority of Deucravacitinib Compared to Placebo and Otezla® (apremilast)
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Bristol-Myers Squibb (BMY) Application for Zeposia for Treatment of Ulcerative Colitis Accepted for Filing with Priority Review by FDA
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Bristol Myers Squibb Application for Zeposia® (ozanimod) for the Treatment of Ulcerative Colitis Accepted for Filing with Priority Review by U.S. Food and Drug Administration
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Bristol-Myers Squibb (BMY) Reports FDA Approval for OPDIVO (nivolumab) in Combination with CABOMETYX (cabozantinib) as First-line Treatment for Patients with Advanced RCC
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U.S. Food and Drug Administration Approves OPDIVO® (nivolumab) in Combination with CABOMETYX® (cabozantinib) as First-line Treatment for Patients with Advanced Renal Cell Carcinoma
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Bristol Myers Squibb Announces Earnings Call Time Change; Fourth Quarter 2020 Earnings Call to Occur on February 4, 2021 at 10 a.m. (Eastern Time)
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Bristol-Myers Squibb (BMY) Announces FDA Accepts for Priority Review Application for Opdivo as Adjuvant Therapy for Patients with Resected Esophageal or Gastroesophageal Junction Cancer
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U.S. Food and Drug Administration Accepts for Priority Review Application for Opdivo® (nivolumab) Combined with Chemotherapy as First-Line Treatment in Metastatic Gastric Cancer, Gastroesophageal Jun
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U.S. Food and Drug Administration Accepts for Priority Review Application for Opdivo® (nivolumab) as Adjuvant Therapy for Patients with Resected Esophageal or Gastroesophageal Junction Cancer
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Bristol-Myers Squibb (BMY) Announces $2 Billion Additional Share Repurchase Authorization
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Bristol Myers Squibb Announces $2 Billion Incremental Share Repurchase Authorization
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Press news Biocartis Group NV: BIOCARTIS MEETS 2020 KEY OBJECTIVES
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Evotec Achieves Milestone in Its Neurodegeneration Collaboration with Bristol Myers Squibb
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Bristol Myers Squibb (BMY) Announces EMA Validates its Application for Opdivo as Adjuvant Treatment for Resected Esophageal or Gastroesophageal Junction Cancer Following Chemoradiotherapy
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Bristol Myers Squibb to Present at J.P. Morgan’s 39th Annual Virtual Healthcare Conference
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European Medicines Agency Validates Bristol Myers Squibb’s Application for Opdivo (nivolumab) Combined with Chemotherapy as First-Line Treatment in Metastatic Gastric Cancer, Gastroesophageal Juncti
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European Medicines Agency Validates Bristol Myers Squibb’s Application for Opdivo (nivolumab) as Adjuvant Treatment for Resected Esophageal or Gastroesophageal Junction Cancer Following Chemoradioth
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Bristol Myers Squibb Provides Update on Status of Contingent Value Rights
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Bristol-Myers Squibb (BMY) Reports EMA Validation of Marketing Authorization Application for Zeposia (ozanimod)
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European Medicines Agency Validates Bristol Myers Squibb’s Application for Zeposia (ozanimod) for the Treatment of Ulcerative Colitis
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Bristol-Myers Squibb (BMY) Phase 3 CheckMate -548 Trial Evaluating Patients with Newly Diagnosed MGMT-Methylated Glioblastoma Multiforme Will Not Meet Primary Endpoint
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Bristol Myers Squibb Announces Update on Phase 3 CheckMate -548 Trial Evaluating Patients with Newly Diagnosed MGMT-Methylated Glioblastoma Multiforme
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Bristol Myers Squibb to Announce Results for Fourth Quarter 2020 on February 4, 2021
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Bristol Myers Squibb Strengthens its Commitment to the Environment with New Corporate Goals
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Cipla Announces Settlement of REVLIMID® (lenalidomide) Capsules Patent Litigation
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Bristol Myers Squibb (BMY) Receives Positive CHMP Opinion for Inrebic for Adult Patients with Newly Diagnosed and Previously Treated Myelofibrosis
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Bristol Myers Squibb Receives Positive CHMP Opinion for Inrebic® (fedratinib) for Adult Patients with Newly Diagnosed and Previously Treated Myelofibrosis
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Bristol-Myers Squibb (BMY) Announces Settlement of U.S. Patent Litigation for REVLIMID with Cipla
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Bristol Myers Squibb Announces Settlement of U.S. Patent Litigation for REVLIMID® (lenalidomide) with Cipla
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Bristol Myers Squibb Announces Dividend Increase
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Checkmate Pharmaceuticals (CMPI) Announces Clinical Collaboration with Bristol Myers Squibb (BMY) to Evaluate CMP-001 in Combination with Nivolumab
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Checkmate Pharmaceuticals Announces Clinical Collaboration with Bristol Myers Squibb to Evaluate CMP-001 in Combination with Nivolumab
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Checkmate Pharmaceuticals Announces Clinical Collaboration with Bristol Myers Squibb to Evaluate CMP-001 in Combination with Nivolumab
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Scripps Research Names Jin-Quan Yu to Newly-Endowed Bristol Myers Squibb Chair in Chemistry
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Bristol Myers Squibb Presents Analyses from Pivotal QUAZAR® AML-001 Study of Onureg® (azacitidine tablets; CC-486) in Adults with Acute Myeloid Leukemia in First Remission
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Bristol Myers Squibb Presents Data Evaluating Potential of Liso-cel Across Leukemia and Lymphomas at ASH 2020
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Bristol Myers Squibb and bluebird bio Present Data Highlighting Anti-BCMA CAR T Cell Therapy, Ide-cel, in Relapsed and Refractory Multiple Myeloma at ASH 2020
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Bristol-Myers Squibb (BMY) Receives EC Approval for Opdivo as Second-Line Treatment for Unresectable Advanced, Recurrent or Metastatic Esophageal Squamous Cell Carcinoma
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Bristol Myers Squibb Receives European Commission Approval for Opdivo (nivolumab) as Second-Line Treatment for Unresectable Advanced, Recurrent or Metastatic Esophageal Squamous Cell Carcinoma
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Schrodinger Inc. (SDGR) Announces Multi-Target Drug Discovery, Development, and Commercialization Collaboration with Bristol Myers Squibb (BMY)
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Schrödinger Announces a Multi-Target Drug Discovery, Development, and Commercialization Collaboration with Bristol Myers Squibb
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Bristol-Myers Squibb (BMY) Completes Acquisition of MyoKardia (MYOK)
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Bristol Myers Squibb Completes Acquisition of MyoKardia, Strengthening Company’s Leading Cardiovascular Franchise
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Veeva Vault PromoMats to Support Bristol Myers Squibb in Speeding Compliant Content to Market
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Veeva Vault PromoMats to Support Bristol Myers Squibb in Speeding Compliant Content to Market Engagement
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Bristol-Myers Squibb (BMY) Provides Regulatory Update on Lisocabtagene Maraleucel

