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Opdivo® (nivolumab) and Yervoy® (ipilimumab) Combination Regimen Shows Clinically Meaningful Responses in First-Line Advanced Non-Small Cell Lung Cancer, In Updated Phase 1b Study CheckMate -012
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Bristol-Myers Squibb to Take Part in Goldman Sachs 37th Annual Global Health Care Conference
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ARIAD Pharma (ARIA) Taps Bristol-Myers Squibb's Herron as Chief Commercial Officer
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Bristol-Myers Squibb to Hold Investor Teleconference to Discuss ASCO Highlights
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Inovalon Announces Agreement with Bristol-Myers Squibb to Focus on Real World Outcomes & Value-Based Contracting Initiatives
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Two-Year Overall Survival Data from Two Pivotal Opdivo® (nivolumab) Trials Demonstrate Sustained Benefit In Patients with Advanced Non-Small Cell Lung Cancer
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Breadth and Depth of Bristol-Myers Squibb’s Immuno-Oncology Clinical Development Program to be Showcased at 2016 American Society of Clinical Oncology (ASCO) Annual Meeting
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Bristol-Myers Squibb (BMY) Affirms FDA Expanded Approval of Opdivo as Treatment of Certain cHL
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Opdivo® (nivolumab) Granted First Approval of a PD-1 Inhibitor in Hematology for the Treatment of Classical Hodgkin Lymphoma Patients Who Have Relapsed or Progressed After Auto-HSCT and Post-transpla
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Bristol-Myers Squibb Opens Expanded Biologics Facility
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Bristol-Myers Squibb (BMY), AbbVie (ABBV) Announce EC Approval of Empliciti Combo as Multiple Myeloma Treatment
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Bristol-Myers Squibb and AbbVie Announce European Commission Approval of Empliciti™ (elotuzumab) for the Treatment of Multiple Myeloma in Adult Patients Who Have Received at Least One Prior Therapy
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Bristol-Myers Squibb (BMY) Receives EC Approval for Opdivo + Yervoy Combo for Treatment of Advanced Melanoma
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European Commission Approves the First and Only Immuno-Oncology Combination, Bristol-Myers Squibb’s Opdivo® (nivolumab) + Yervoy® (ipilimumab) Regimen, for Treatment of Advanced Melanoma
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Modern Family Star Eric Stonestreet and His Mom, a Two Time Cancer Survivor, Join Forces to Raise Awareness of Immuno-Oncology Research through Ready. Raise. Rise. Campaign
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Bristol-Myers Squibb Reports First Quarter Financial Results
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Bristol-Myers Squibb to Take Part in Deutsche Bank Annual Health Care Conference
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Bristol-Myers Squibb's (BMY) Opdivo Granted FDA Breakthrough Therapy Designation in Metastatic SCCHN
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Bristol-Myers Squibb’s Opdivo® (nivolumab) Receives Breakthrough Therapy Designation from U.S. Food and Drug Administration for Previously Treated Recurrent or Metastatic Squamous Cell Carcinoma of
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Medidata Solutions (MDSO) Announces Bristol-Myers Squibb (BMY) Selected Medidata Clinical Cloud
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Bristol-Myers Squibb Selects Medidata Clinical Cloud® to Drive Drug Development and Business Transformation
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Bristol-Myers Squibb (BMY) Announces Presentation of Significant Opdivo Phase 3 Data in SCCHN
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First Presentation of Overall Survival Data for Opdivo® (nivolumab) Shows Significant Survival Benefit at One-Year Versus Investigator’s Choice in Recurrent or Metastatic Squamous Cell Carcinoma of
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First Presentation of Two-Year Overall Survival Data for Opdivo® (nivolumab) in Combination with Yervoy® (ipilimumab) Showed Superior Efficacy Versus Yervoy Alone in Advanced Melanoma
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Bristol-Myers Squibb (BMY) Announces U.S. FDA Acceptance of Opdivo sBLA fro cHL Following Therapies
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U.S. Food and Drug Administration Accepts for Priority Review Bristol-Myers Squibb’s Supplemental Biologics License Application for Opdivo® (nivolumab) for the Treatment of Classical Hodgkin Lympho
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Bristol-Myers Squibb (BMY) Opdivo Approved in Europe for Advanced RCC
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European Commission Approves Bristol-Myers Squibb’s Opdivo® (nivolumab) for Previously Treated Advanced Renal Cell Carcinoma
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Bristol-Myers Squibb (BMY) Announces EC Approval of Expanded Opdivo Indication
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European Commission Approves Expanded Use of Opdivo® (nivolumab) to Include Previously Treated Metastatic Non-Squamous Non-Small Cell Lung Cancer
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Bristol-Myers Squibb (BMY) Announces Completion of Padlock Therapeutics Acquisition
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Bristol-Myers Squibb Completes Previously Announced Acquisition of Padlock Therapeutics, Inc.
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Bristol-Myers Squibb Receives Positive CHMP Opinion for Opdivo® (nivolumab) in Combination with Yervoy® (ipilimumab) for Treatment of Advanced Melanoma
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Bristol-Myers Squibb (BMY) Announces EMA Validation of Opdivo-Related Type 2 Variation Application
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European Medicines Agency Validates Bristol-Myers Squibb’s Application for Opdivo® (nivolumab) for the Treatment of Classical Hodgkin Lymphoma Patients
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Pfizer (PFE), Bristol-Myers Squibb (BMY) Will Present 16 Abstracts at ACC.16
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Bristol-Myers Squibb and Pfizer Announce Global Real-World Data Program and Present New Analyses of Eliquis (apixaban) at the American College of Cardiology’s 65th Annual Scientific Session
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Bristol-Myers Squibb to Present at William Blair Conference, Cancer Immunotherapy: A Long-Awaited Reality
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Bristol-Myers Squibb (BMY) Enters Agreement to Acquire Padlock Therapeutics in ~$600M Deal
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Bristol-Myers Squibb to Acquire Padlock Therapeutics, Inc.
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Bristol-Myers Squibb (BMY) Will Present New Opdivo, Yervoy Data Overall Survival Data at AACR 2016
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Bristol-Myers Squibb to Present New Overall Survival Data for Opdivo® (nivolumab) as Monotherapy and in Combination with Yervoy® (ipilimumab) at the AACR 2016 Annual Meeting
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Allied-Bristol Life Sciences Launches iβeCa Therapeutics from NYU School of Medicine to Develop Novel Cancer Therapeutics Targeting the Wnt Pathway
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Bristol-Myers Squibb to Announce Results for First Quarter 2016 on April 28
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Bristol-Myers Squibb to Present at Barclays Global Health Care Conference
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Bristol-Myers Squibb and LabCentral Team Up in Cambridge, Massachusetts to Support Promising Biotech Startup Companies
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Bristol-Myers Squibb Announces Dividend
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Bristol-Myers Squibb (BMY) Adds Integra LifeSciences CEO Arduini as Director
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Bristol-Myers Squibb Names Peter J. Arduini to Board of Directors
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Bristol-Myers Squibb to Present at Cowen and Company Annual Global Health Care Conference

