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Research from Bristol-Myers Squibb’s Innovative Oncology Development Program to Be Presented at AACR 2018 Demonstrates Commitment to Advancing Precision Medicine Research for Patients with Cancer
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Bristol-Myers Squibb to Announce Results for First Quarter 2018 on April 26
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GRYT Health and Bristol-Myers Squibb Announce New Digital Pilot to Advance Cancer Care through Patient-Driven Insights
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Findings Released from Largest Real-World Data Analysis of Non-Valvular Atrial Fibrillation Patients Receiving Direct Oral Anticoagulants
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Bristol-Myers Squibb to Take Part in Barclays Global Healthcare Conference
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Bristol-Myers Squibb (BMY) Says Opdivo Now First and Only FDA-Approved PD-1 Inhibitor to Offer Every Four-Week Dosing
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Bristol-Myers Squibb’s Opdivo® (nivolumab) Now the First and Only FDA-Approved PD-1 Inhibitor to Offer Every Four-Week Dosing
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Bristol-Myers Squibb to Take Part in Cowen and Company 38th Annual Global Health Care Conference
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Bristol-Myers Squibb Announces Dividend Increase
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Bristol-Myers Squibb Names José Baselga, M.D., Ph.D. to Board of Directors
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Bristol-Myers Squibb Announces Expansion of the International Immuno-Oncology Network (II-ON) with Addition of Yale Cancer Center
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Bristol-Myers Squibb (BMY), Nektar Therapeutics (NKTR) to Partner on NKTR-214 in $1.85B+ Deal
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Bristol-Myers Squibb and Nektar Therapeutics Announce Global Development & Commercialization Collaboration for Nektar’s CD122-biased Agonist, NKTR-214
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Bristol-Myers Squibb to Take Part in Leerink 7th Annual Global Healthcare Conference
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Bristol-Myers Squibb (BMY) Reports Pivotal Phase 3 CheckMate-227 Study Provides Superior Progression-Free Survival (PFS) with the Opdivo Plus Yervoy Combination
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Pivotal Phase 3 CheckMate -227 Study Demonstrates Superior Progression-Free Survival (PFS) with the Opdivo Plus Yervoy Combination Versus Chemotherapy in First-Line Non-Small Cell Lung Cancer (NSCLC)
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Bristol-Myers Squibb Reports Fourth Quarter and Full Year Financial Results
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Five Prime Therapeutics (FPRX) Announces $25 Million Payment by Bristol-Myers Squibb (BMY) for Cabiralizumab Development Milestone
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Five Prime Therapeutics Announces $25 Million Payment by Bristol-Myers Squibb for Cabiralizumab Development Milestone
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Bristol-Myers Squibb (BMY) Reports EC Approval for its Yervoy for Treatment of Pediatric Patients 12 Years and Older with Unresectable or Metastatic Melanoma
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European Commission Approves Bristol-Myers Squibb’s Yervoy (ipilimumab) for Treatment of Pediatric Patients 12 Years and Older with Unresectable or Metastatic Melanoma
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Bristol-Myers Squibb (BMY) Reports Updated Data for Phase 2 CheckMate -142 Trial Evaluating Opdivo (nivolumab) and Yervoy (ipilimumab)
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Opdivo (nivolumab) in Combination with Yervoy (ipilimumab) Demonstrates Clinical Activity in Previously Treated Patients with dMMR or MSI-H Metastatic Colorectal Cancer
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Five Prime Therapeutics (FPRX) Secures $5M IND Milestone Payment from Bristol-Myers Squibb (BMY) Under Immune Checkpoint Pathways Discovery Collaboration; BMY to Extend Term for 2nd Time
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Five Prime Therapeutics Earns IND Milestone Payment Under Immune Checkpoint Pathways Discovery Collaboration with Bristol-Myers Squibb and Announces that BMS has Extended the Research Term of this Col
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Bristol-Myers Squibb to Present at J.P. Morgan Healthcare Conference
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Bristol-Myers Squibb (BMY) Announces FDA Approval for Opdivo as Adjuvant Therapy in Patients with Completely Resected Melanoma with Lymph Node Involvement or Metastatic Disease
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Bristol-Myers Squibb Receives FDA Approval for Opdivo (nivolumab) as Adjuvant Therapy in Patients with Completely Resected Melanoma with Lymph Node Involvement or Metastatic Disease
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Bristol-Myers Squibb (BMY) Announces Clinical Trial Collaboration with TARIS Biomedical LLC
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TARIS and Bristol-Myers Squibb Announce Clinical Trial Collaboration
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Bristol-Myers Squibb to Announce Results for Fourth Quarter 2017 on February 5th
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Bristol-Myers Squibb (BMY) Receives Positive CHMP Opinion Recommending Approval of Yervoy for the Treatment of Pediatric Patients 12 Years and Older with Unresectable or Metastatic Melanoma
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Bristol-Myers Squibb Receives Positive CHMP Opinion Recommending Approval of Yervoy (ipilimumab) for the Treatment of Pediatric Patients 12 Years and Older with Unresectable or Metastatic Melanoma
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Bristol-Myers Squibb (BMY) Announces Exclusive Licensing Agreement with Ono Pharmaceutical for Multiple Programs Targeting Immuno-Suppressive Factors in the Tumor Microenvironment
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Bristol-Myers Squibb Granted Exclusive License by Ono Pharmaceutical for Multiple Programs Targeting Immuno-Suppressive Factors in the Tumor Microenvironment
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Bristol-Myers Squibb (BMY) Announces FDA Accepts its Application for Opdivo Plus Yervoy in Intermediate- and Poor-Risk Patients with Advanced RCC and Grants Priority Review
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U.S. Food and Drug Administration (FDA) Accepts Bristol-Myers Squibb’s Application for Opdivo (nivolumab) Plus Yervoy (ipilimumab) in Intermediate- and Poor-Risk Patients with Advanced Renal Cell Ca
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Seattle Genetics (SGEN), Bristol-Myers Squibb (BMY) Highlight Interim Results from Phase 1/2 Study Evaluating the Combination of ADCETRIS and Opdivo in R/R Hodgkin Lymphoma
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Seattle Genetics and Bristol-Myers Squibb Highlight Interim Results from Phase 1/2 Study Evaluating the Combination of ADCETRIS® (Brentuximab Vedotin) and Opdivo® (Nivolumab) in Relapsed or Refracto
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Sprycel (dasatinib) Added to Standard Chemotherapy Demonstrates Three-Year Survival Benefit in Pediatric Patients with Newly Diagnosed Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia
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Bristol-Myers Squibb Announces Dividend Increase
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Bristol-Myers Squibb (BMY) Says CheckMate -078 Phase 3 Opdivo Lung Cancer Trial with Predominantly Chinese Patients Stopped Early for Demonstrating Superior Overall Survival
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CheckMate -078, a Pivotal, Multinational Phase 3 Opdivo (nivolumab) Lung Cancer Trial with Predominantly Chinese Patients, Stopped Early for Demonstrating Superior Overall Survival
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Bristol-Myers Squibb to Take Part at the Citi 2017 Global Healthcare Conference
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Bristol-Myers Squibb (BMY) Announces 33 Presentations at ASH
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Bristol-Myers Squibb to Present New Data Across a Broad Range of Blood Cancers at the 59th Annual Meeting & Exposition of the American Society of Hematology
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Bristol-Myers Squibb Awards “Golden Tickets” for LabCentral to Neutrolis, Remora Therapeutics
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Bristol-Myers Squibb (BMY) Says EMA Validated its Type II Variation Application for Opdivo Plus Yervoy in Intermediate- and Poor-Risk Patients with Advanced RCC
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European Medicines Agency Validates Bristol-Myers Squibb’s Type II Variation Application for Opdivo (nivolumab) Plus Yervoy (ipilimumab) in Intermediate- and Poor-Risk Patients with Advanced Renal C
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Bristol-Myers Squibb to Take Part in Evercore ISI Biopharma Conference

