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Bristol-Myers Squibb to Announce Results for Third Quarter 2017 on October 26
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CheckMate -214 Study Evaluating Opdivo in Combination with Yervoy Stopped Early for Demonstrating Overall Survival Benefit in Patients with Previously Untreated Advanced or Metastatic Renal Cell Carci
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Bristol-Myers Squibb Employees Ride Across the U.S. to Raise Money to Support Cancer Research by Stand Up To Cancer
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Bristol-Myers Squibb to Take Part in Morgan Stanley Global Health Care Conference
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Bristol-Myers Squibb Data at ESMO 2017 Demonstrate Company’s Innovative Research Approach to Treating Cancer from All Angles
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Pfizer (PFE) & Bristol-Meyers Squibb (BMY) Report Positive Real-World Data for Eliquis (Apixaban) Compared to Warfrin in Patients Over 65 with NVAF
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Bristol-Myers Squibb and Pfizer Alliance Announce Real-World Observational Analysis of the Effectiveness and Safety of Direct Oral Anticoagulants Compared to Warfarin in Elderly Patients with Non-Valv
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Bristol-Myers Squibb (BMY), Daiichi Sankyo Announce Pact to Evaluate Opdivo and DS-8201 in HER2-Expressing Breast and Bladder Cancers
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Bristol-Myers Squibb and Daiichi Sankyo Announce Research Collaboration to Evaluate Opdivo® (nivolumab) and DS-8201 in HER2-Expressing Breast and Bladder Cancers
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Pfizer (PFE) & Bristol-Myers Squibb (BMY) Report Results of Observational Real-World Data Analysis on the Effectiveness and Safety of Eliquis
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Bristol-Myers Squibb and Pfizer Present Investigational Eliquis® (apixaban) Data for Patients with Non-Valvular Atrial Fibrillation (NVAF) Undergoing Cardioversion
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Bristol-Myers Squibb and Pfizer Present Observational Real-World Data Analysis on the Effectiveness and Safety of Eliquis® (apixaban) Compared to Warfarin in Select High-Risk Patients with Non-Valvul
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Bristol-Myers Squibb (BMY), Pfizer (PFE) to Highlight Commitment to Reducing Risk of Stroke Caused by NVAF and Treating DVT/PE at ESC Congress
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Bristol-Myers Squibb and Pfizer to Highlight Commitment to Reducing the Risk of Stroke Caused by Non-Valvular Atrial Fibrillation (NVAF) and Treating Deep Vein Thrombosis/Pulmonary Embolism (DVT/PE) a
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Bristol-Myers Squibb (BMY) Says CheckMate -214 Combination Study Met Co-primary Endpoint of ORR but PFS Didn't Reach Statistical Significance
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Bristol-Myers Squibb Announces Topline Results from CheckMate -214, a Phase 3 Study of Opdivo in Combination with Yervoy in Intermediate and Poor-Risk Patients with Previously Untreated Advanced or Me
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Bristol-Myers Squibb (BMY) to Acquire IFM Therapeutics
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Bristol-Myers Squibb to Acquire IFM Therapeutics to Strengthen Oncology Pipeline Focus on Innate Immunity
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Bristol-Myers Squibb (BMY) Announces FDA Approval for Opdivo in MSI-H or dMMR Metastatic Colorectal Cancer
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Bristol-Myers Squibb Receives FDA Approval for Opdivo (nivolumab) in MSI-H or dMMR Metastatic Colorectal Cancer That Has Progressed Following Treatment with a Fluoropyrimidine, Oxaliplatin, and Irinot
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Bristol-Myers Squibb (BMY), Clovis Oncology (CLVS) Enter Clinical Collaboration to Evaluate Combination of Opdivo and Rubraca in Phase 2 and Pivotal Phase 3 Clinical Trials in Tumors
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Bristol-Myers Squibb and Clovis Oncology Announce a Broad Clinical Collaboration to Evaluate Combination of Opdivo (Nivolumab) and Rubraca® (Rucaparib) in Phase 2 and Pivotal Phase 3 Clinical Trials
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Tech, transports drag on Wall Street; Dow hits record
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Bristol-Myers Squibb Reports Second Quarter Financial Results
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Bristol-Myers Squibb’s ORENCIA® (abatacept) Receives Second European Commission Approval in Less than a Year – New Approval for Treatment of Active Psoriatic Arthritis (PsA)1
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Bristol-Myers Squibb (BMY) Says FDA Accepts Applications for Opdivo Four-Week Dosing Schedule Across All Approved Indications
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U.S. Food and Drug Administration Accepts Bristol-Myers Squibb’s Applications for Opdivo (nivolumab) Four-Week Dosing Schedule Across All Approved Indications
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Bristol-Myers Squibb (BMY) Granted Expanded Approval by FDA of Yervoy (ipilimumab) to Include Pediatric Patients 12 Years & Older with Unresectable or Metastatic Melanoma
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U.S. Food and Drug Administration Expands Approval of Yervoy® (ipilimumab) to Include Pediatric Patients 12 Years and Older with Unresectable or Metastatic Melanoma
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Bristol-Myers Squibb (BMY) & Exelis (EXEL) Commence Phase 3 Trial of Opdivo in Combination with CABOMETYX or Opdivo & Yervoy in Combination with CABOMETYX
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Exelixis and Bristol-Myers Squibb Initiate Phase 3 Trial of Opdivo® in Combination with CABOMETYX™ or Opdivo and Yervoy® in Combination with CABOMETYX, Versus Sunitinib in Previously Untreated Adv
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Bristol-Myers Squibb (BMY) Announces FDA Accepts Priority Review Application for Sprycel in Children with Philadelphia Chromosome-Positive CP Chronic Myeloid Leukemia
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U.S. Food and Drug Administration Accepts for Priority Review Bristol-Myers Squibb’s Application for Sprycel (dasatinib) in Children with Philadelphia Chromosome-Positive Chronic Phase Chronic Myelo
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Bristol-Myers Squibb’s ORENCIA (abatacept) Receives FDA Approval for Treatment of Active Psoriatic Arthritis (PsA) in Adults
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Bristol-Myers Squibb (BMY) Reports Phase 3 Study Evaluating Opdivo in Resected High-Risk Melanoma Patients Meets Primary Endpoint
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Phase 3 Study Evaluating the Safety and Efficacy of Adjuvant Opdivo in Resected High-Risk Melanoma Patients Meets Primary Endpoint
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Modern Family Star Eric Stonestreet Challenges Americans to Support the Cancer Community and Learn about Immuno-Oncology Research Through Ready. Raise. Rise.
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Four-Year Follow-up with Empliciti (elotuzumab) Plus Lenalidomide/Dexamethasone (ELd) in Patients with Advanced Multiple Myeloma Shows Long-term Efficacy in ELOQUENT-2 Trial
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Bristol-Myers Squibb Announces the Expiration of its Cash Tender Offer
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Bristol-Myers Squibb Announces the Pricing Terms of its Cash Tender Offer For Any and All of Certain of its Outstanding Debt Securities
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Bristol-Myers Squibb (BMY) Presents Extended Follow-Up Data Evaluating Opdivo (nivolumab)
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Extended Follow-Up Data Evaluating Opdivo (nivolumab) Shows Durable Response in Adult Patients with Relapsed or Progressed Classical Hodgkin Lymphoma
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Bristol-Myers Squibb (BMY) Agrees to Sell Manufacturing Facility in Ireland to SK Biotek Co.; Terms Not Disclosed
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Bristol-Myers Squibb to Sell Manufacturing Facility in Swords, Ireland to SK Biotek Co., Ltd.
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Seattle Genetics (SGEN) and Bristol-Myers Squibb (BMY) Highlight Interim Phase 1/2 Data Evaluating Combination of ADCETRIS (Brentuximab Vedotin) & Opdivo (Nivolumab)
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Seattle Genetics and Bristol-Myers Squibb Highlight Interim Phase 1/2 Data Evaluating Combination of ADCETRIS® (Brentuximab Vedotin) and Opdivo® (Nivolumab) in Relapsed Hodgkin Lymphoma at the Inter
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Bristol-Myers Squibb Announces Cash Tender Offer For Any and All of Certain of Its Outstanding Debt Securities
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Bristol-Myers Squibb (BMY) to Present Research on RA Patients With Highly Active, Progressive Disease at EULAR 2017
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Bristol-Myers Squibb To Present New Research Related to the Treatment of Rheumatoid Arthritis Patients With Highly Active, Progressive Disease at the Annual European Congress of Rheumatology (EULAR 2
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Bristol-Myers Squibb Announces Dividend

