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Bristol-Myers Squibb (BMY) Reports Positive Phase 2 Data for BMS-986036 (Pegylated FGF21)
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Bristol-Myers Squibb’s BMS-986036 (Pegylated FGF21) Shows Consistent Improvement in Liver Fat, Liver Injury and Fibrosis in Patients with Nonalcoholic Steatohepatitis (NASH) in Phase 2 Trial
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Bristol-Myers Squibb (BMY) Announces Positive CHMP Opinion Recommending Approval of Opdivo to Treat Locally Advanced or mUC
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Bristol-Myers Squibb Receives Positive CHMP Opinion Recommending Approval of Opdivo (nivolumab) for the Treatment of Patients with Previously Treated Locally Advanced or Metastatic Urothelial Carcinom
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Bristol-Myers Squibb and Nordic Bioscience Announce Collaboration for Fibrosis Biomarker Technology
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Biogen (BIIB) Confirms Agreement to License Phase 2 Anti-Tau Antibody from Bristol-Myers Squibb (BMY)
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Bristol-Myers Squibb (BMY) Enters Agreements to License Anti-eTau, Anti-Myostatin Compounds to Biogen (BIIB), Roche
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Biogen Licenses Phase 2 Anti-Tau Antibody from Bristol-Myers Squibb
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Bristol-Myers Squibb Enters into Separate Agreements with Biogen and Roche to License Anti-eTau and Anti-Myostatin Compounds, Respectively
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Bristol-Myers Squibb (BMY) Announces Collaboration with Apexigen for Opdivo Combination with APX005M
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Bristol-Myers Squibb and Apexigen, Inc. Announce Clinical Collaboration to Evaluate Opdivo (nivolumab) in Combination with APX005M in Advanced Solid Tumors
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Bristol-Myers Squibb (BMY) Confirms FDA Accepts Supplemental Biologics License Application (sBLA) to Extend use of Opdivo in Previously Treated dMMR or MSI-H Metastatic Colorectal Cancer
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U.S. Food and Drug Administration Accepts for Priority Review Bristol-Myers Squibb’s Application for Opdivo (nivolumab) in Previously Treated dMMR or MSI-H Metastatic Colorectal Cancer
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Bristol-Myers Squibb (BMY) Says Opdivo CheckMate -143 Did Not Meet Primary Endpoint
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Bristol-Myers Squibb Announces Results from CheckMate -143, a Phase 3 Study of Opdivo (nivolumab) in Patients with Glioblastoma Multiforme
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Bristol-Myers Squibb (BMY) Announces First Report of 5-yr (OS) Data from Phase 1 Dose-Ranging Study CA209-003 Evaluating Opdivo
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Bristol-Myers Squibb (BMY) Announces First (OS) Data from the Phase 3 CheckMate -067 Clinical Trial
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Opdivo (nivolumab) in Combination with Yervoy (ipilimumab) and Opdivo Monotherapy Significantly Improved Overall Survival Versus Yervoy Alone in Patients with Previously Untreated Advanced Melanoma
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Five-Year Survival Observed With Opdivo (nivolumab) in Patients With Previously Treated Advanced Non-Small Cell Lung Cancer (NSCLC), in Phase 1 Study CA209-003
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Bristol-Myers Squibb (BMY) and Incyte (INCY) Advance Epacadostat and Opdivo Combo
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Bristol-Myers Squibb and Incyte to Advance the Combination of Opdivo (nivolumab) and Epacadostat into First-line Registrational Trials
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Bristol-Myers Squibb (BMY), Foundation Medicine (FMI) Enter Pact to Identify Predictive Biomarkers Across Multiple Tumor Types and Immunotherapy Agents
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Bristol-Myers Squibb Enters Collaboration to Leverage Foundation Medicine’s Molecular Information Platform to Identify Predictive Biomarkers Across Multiple Tumor Types and Immunotherapy Agents
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Bristol-Myers Squibb (BMY), CRI, and Parker Institute for Cancer Immunotherapy Enter Research Pact
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Parker Institute for Cancer Immunotherapy, Bristol-Myers Squibb and the Cancer Research Institute Announce Collaboration to Accelerate Immuno-Oncology Research
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Bristol-Myers Squibb (BMY) Announces Positive CHMP Opinion of Opdivo for Treatment of SCCHN in Adults Progressing on or After Platinum-based Therapy
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Bristol-Myers Squibb Receives Positive CHMP Opinion Recommending Opdivo (nivolumab) for the Treatment of Squamous Cell Cancer of the Head and Neck in Adults Progressing on or After Platinum-based Ther
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Bristol-Myers Squibb (BMY), CtomX Therapeutics (CTMX) Extend Strategic Collaboration
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Bristol-Myers Squibb and CytomX Therapeutics Extend Worldwide Collaboration to Discover Probody™ Therapeutics for the Treatment of Cancer and Other Diseases
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Bristol-Myers Squibb (BMY), Pfizer (PFE) Present Analysis of Effectiveness and Safety of Direct Oral Anticoagulants Compared to Warfarin in Patients with Non-Valvular Atrial Fibrillation
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Bristol-Myers Squibb and Pfizer Present Large Real-World Observational Analysis of the Effectiveness and Safety of Direct Oral Anticoagulants Compared to Warfarin in Patients with Non-Valvular Atrial
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Bristol-Myers Squibb to Announce Results for First Quarter 2017 on April 27
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Bristol-Myers Squibb (BMY) Names Lynch EVP/CSO as Cuss Retires
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Bristol-Myers Squibb Appoints Dr. Thomas J. Lynch, Jr., Executive Vice President and Chief Scientific Officer
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Bristol-Myers Squibb to Take Part in Barclays Global Health Care Conference
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Bristol-Myers Squibb (BMY), Pfizer (PFE) to Present New Analyses of Eliquis and Real-World Data at ACC
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Bristol-Myers Squibb and Pfizer to Present New Analyses of Eliquis™ (apixaban) Clinical and Real-World Data at the American College of Cardiology 2017 Scientific Session
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Bristol-Myers Squibb Announces Dividend
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Bristol-Myers Squibb to Present Data That Advances Understanding of Effects of Immuno-Oncology Therapies on Cancer Biology and Patient Outcomes at AACR 2017
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Bristol-Myers Squibb (BMY) Announces Investment and Planned Collaboration with GRAIL on Blood-Based Cancer Screening
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Bristol-Myers Squibb Expands Focus on Precision Medicine with Investment and Planned Collaboration with GRAIL on Blood-Based Cancer Screening
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Bristol-Myers Squibb to Take Part in Cowen and Company 37th Annual Global Health Care Conference
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Bristol-Myers Squibb (BMY) Adds Columbia University Medical Center and Peter MacCallum Cancer Centre to II-ON
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Exelixis (EXEL), Bristol-Myers Squibb (BMY) Enter Clinical Collaboration for Late-Stage Combination Trial in First-Line Renal Cell Carcinoma
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Bristol-Myers Squibb Expands International Immuno-Oncology Network (II-ON) With Addition of Columbia University Medical Center and Peter MacCallum Cancer Centre
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Exelixis and Bristol-Myers Squibb Enter Clinical Collaboration for Late-Stage Combination Trial in First-Line Renal Cell Carcinoma
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Bristol-Myers Squibb Prices $1.5 Billion of Senior Notes
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Bristol-Myers Squibb (BMY) Announces $2B Accelerated Share Repurchase and Names Three New Independent Directors in Agreement with JANA
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Bristol-Myers Squibb Appoints Three New Independent Directors
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JANA Partners Enters Aetna (AET), Bristol-Myers Squibb (BMY), Lamb Weston (LW), Salesforce (CRM) (more...) - 13F

