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Bristol-Myers Squibb Selects Veeva Vault RIM Solutions
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Bristol-Myers Squibb (BMY) Announces Two Positive CHMP Opinions for Opdivo for Treatment of NSCLC
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Bristol-Myers Squibb Receives Two Positive CHMP Opinions for Opdivo® (nivolumab) for Patients with Previously Treated Advanced Non-Squamous Non-Small Cell Lung Cancer and Renal Cell Carcinoma
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Bristol-Myers Squibb (BMY) Announces Completion of HIV R&D Portfolio Sale to ViiV Healthcare
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Bristol-Myers Squibb Completes Previously Announced Sale of its HIV R&D Portfolio to ViiV Healthcare
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Data Presented at APASL from First Completed Phase 3 Trial of All-oral Chronic Hepatitis C Regimen in Chinese Patient Population Shows Daclatasvir and Asunaprevir DUAL Therapy Demonstrated High Cure R
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Bristol-Myers Squibb (BMY), Dana-Farber Cancer Institute Enter I-O RPM Program Collaboration
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Bristol-Myers Squibb and Dana-Farber Cancer Institute Enter Into a Collaboration Agreement as Part of U.S. Immuno-Oncology Rare Population Malignancy Research Program
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Bristol-Myers Squibb (BMY) Receives FDA Approval for Expanded Daklinza Indication in Genotype 1, 3 HCV
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U.S. FDA Approves Expanded Use of Bristol-Myers Squibb’s Daklinza (daclatasvir) for Additional Challenging-to-treat Patients with Genotype 1 or Genotype 3 Chronic Hepatitis C
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Bristol-Myers Squibb to Take Part in Leerink Swann Global Healthcare Conference
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Bristol-Myers Squibb Foundation Awards Eight Grants Totaling Nearly $11.5M to Make Lung and Skin Cancer Screening, Care More Accessible in High-Risk U.S. Communities
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Portola Pharma (PTLA) Enters Licensing Agreements for Investigational Agent Andexanet in Japan (BMY) (PFE)
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Bristol-Myers Squibb and Pfizer Sign Collaboration with Portola Pharmaceuticals to Develop and Commercialize Investigational Andexanet Alfa in Japan
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Bristol-Myers Squibb (BMY), AbbVie (ABBV) Announce Receipt of Positive CHMP Opinion for Empliciti as Multiple Myeloma Treatment
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Bristol-Myers Squibb and AbbVie Receive Positive CHMP Opinion for Investigational Antibody, Empliciti (elotuzumab), for the Treatment of Multiple Myeloma in Patients Who Have Received at Least One Pri
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Bristol-Myers Squibb (BMY) Announces Receipt of EC Approval for Daklinza in Certain HCV Genotypes
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European Commission Approves Daklinza (daclatasvir) for the Treatment of Genotype 1, 3 and 4 Chronic Hepatitis C Patients with HIV Coinfection, Advanced Cirrhosis and Post-liver Transplant Recurrence
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Bristol-Myers Squibb (BMY) Announces Early Stoppage of Opdivo Phase 3 in SCCHN
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Bristol-Myers Squibb Reports Fourth Quarter and Full Year 2015 Financial Results
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CheckMate -141, a Pivotal Phase 3 Opdivo (nivolumab) Head and Neck Cancer Trial, Stopped Early
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REPEAT/ Bristol-Myers Squibb’s Opdivo (nivolumab) + Yervoy (ipilimumab) Regimen Receives Expanded FDA Approval in Unresectable or Metastatic Melanoma Across BRAF Status1
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Bristol-Myers Squibb (BMY) Receives FDA Approval for Expanded Opdivo + Yervoy Combo Indication
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Bristol-Myers Squibb’s Opdivo (nivolumab) + Yervoy (ipilimumab) Regimen Receives Expanded FDA Approval in Unresectable or Metastatic Melanoma Across BRAF Status1
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Bristol-Myers Squibb to Present at J.P. Morgan Healthcare Conference
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Seattle Genetics (SGEN), Bristol-Myers Squibb (BMY) Initiate ADCETRIS + Opdivo Phase 1/2 in DLBCL
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Seattle Genetics and Bristol-Myers Squibb Announce Initiation of Phase 1/2 Clinical Trial of ADCETRIS® (Brentuximab Vedotin) in Combination with Opdivo® (Nivolumab) in Relapsed or Refractory Non-Hod
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ViiV Healthcare to Acquire Bristol-Myers Squibb's (BMY) Investigational HIV Medicines Pipeline
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Bristol-Myers Squibb to Sell its HIV R&D Portfolio to ViiV Healthcare
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BMS and The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute Enter Into a Collaboration Agreement as Part of U.S. Immuno-O
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Bristol-Myers Squibb (BMY), UCLA Enter I-O RPM Research Program Collaboration
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Bristol-Myers Squibb and UCLA Enter into a Collaboration Agreement as Part of U.S. Immuno-Oncology Rare Population Malignancy Research Program
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Bristol-Myers Squibb to Announce Results for Fourth Quarter, Full Year 2015 on January 28
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Bristol-Myers Squibb (BMY) , Pfizer (PFE) Announce Encouraging Post-Hoc Data from Phase 3 AMPLIFY in VTE
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AMPLIFY Post-Hoc Early Time Course Analysis Evaluated Recurrent Venous Thromboembolism (VTE), VTE-Related Death and Major Bleeding in Deep Vein Thrombosis and Pulmonary Embolism Patients Treated with
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Bristol-Myers Squibb Completes Previously Announced Acquisition of Cardioxyl Pharmaceuticals, Inc.
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Bristol-Myers Squibb (BMY) Enters Research Collaboration with Princeton University Dept. of Chemistry
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Bristol-Myers Squibb Establishes Center for Molecular Synthesis in New Collaboration with Princeton University
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Bristol-Myers Squibb Announces Dividend Increase
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New Longer-Term Data for Empliciti (elotuzumab) Showed a Continued Progression-Free Survival Benefit in Patients with Relapsed or Refractory Multiple Myeloma
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Bristol-Myers Squibb Receives Multiple Myeloma Research Foundation’s 2015 Collaborator Award
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Bristol-Myers Squibb Foundation Marks World AIDS Day with Grants Totaling More than $3.5M for HIV and Cervical and Breast Cancer Programs in Africa
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Bristol-Myers Squibb and AbbVie Receive FDA Approval of Empliciti™ (elotuzumab) for the Treatment of Patients with Multiple Myeloma Who Have Received One to Three Prior Therapies
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Bristol-Myers Squibb to Present New Data across Multiple Blood Cancers at the 57th Annual Meeting & Exposition of the American Society of Hematology
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Bristol-Myers Squibb Announces Regulatory Update for Opdivo (nivolumab) in Advanced Melanoma
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European Commission Approves Reconciliation of Indications for nivolumab Under the Opdivo® European Marketing Authorization Application
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Bristol-Myers Squibb Announces U.S. Food and Drug Administration Approval for Opdivo (nivolumab) as a Single Agent for the Treatment of Patients with Previously Untreated BRAF Wild-Type Advanced Melan
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Bristol-Myers Squibb Receives FDA Approval for Opdivo (nivolumab), the Only Treatment to Deliver Significant Overall Survival in Advanced Renal Cell Carcinoma vs. a Standard of Care, in Patients Who H
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New Long-Term Data on Opdivo and the Opdivo + Yervoy Regimen Shows Survival Benefit Across Lines of Therapy in Advanced Melanoma
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U.S. Food and Drug Administration Accepts for Priority Review the Supplemental Biologics License Application for Opdivo (nivolumab) in Patients with Advanced Renal Cell Carcinoma

