2014 News Releases

2014 | 2013 | 2012
07/10/14Bristol-Myers Squibb Announces Plans for Third Quarter Submission of a Biologics License Application for Opdivo® (nivolumab), an Investigational PD-1 Immune Checkpoint Inhibitor, for Previously Treated Advanced MelanomaPrinter Friendly Version
07/07/14Japan Approves First All-Oral, Interferon- and Ribavirin-Free Hepatitis C Treatment, Daklinza® (daclatasvir) and Sunvepra® (asunaprevir) Dual RegimenPrinter Friendly Version
07/01/14Bristol-Myers Squibb to Announce Results for Second Quarter on July 24Printer Friendly Version
06/27/14Eliquis® (apixaban) Receives CHMP Positive Opinion for the Treatment of Deep Vein Thrombosis (DVT) and Pulmonary Embolism (PE), and Prevention of Recurrent DVT and PEPrinter Friendly Version
06/27/14Bristol-Myers Squibb Receives Positive CHMP Opinion for Daklinza® (daclatasvir) for Treatment of Chronic Hepatitis C in the European UnionPrinter Friendly Version
06/24/14Phase 3 First-Line Melanoma Study of Nivolumab, an Investigational PD-1 Checkpoint Inhibitor, Demonstrates Superior Overall Survival Compared to Dacarbazine; Study Stopped EarlyPrinter Friendly Version
06/24/14Bristol-Myers Squibb Expands Access to Clinical Trial Data Through Collaboration with Academic Research InstitutePrinter Friendly Version
06/17/14Bristol-Myers Squibb Announces DividendPrinter Friendly Version
06/12/14U.S. Court of Appeals Denies Appeal in Baraclude Patent CasePrinter Friendly Version
06/10/14AVERT Trial Demonstrates High Rates of DAS-defined Remission with Orencia® (abatacept) in Combination with Methotrexate (MTX) in Adult Patients with Early Rheumatoid Arthritis (RA)Printer Friendly Version
06/09/14Giovanni Caforio, M.D., Appointed Chief Operating Officer and Elected to Board of DirectorsPrinter Friendly Version
06/03/14Bristol-Myers Squibb to Take Part in Goldman Sachs 35th Annual Global Health Care ConferencePrinter Friendly Version
06/03/14Bristol-Myers Squibb and Syngene International Extend Research CollaborationPrinter Friendly Version
06/02/14Phase 3 Study Evaluating Yervoy® (Ipilimumab) for Melanoma in an Adjuvant Setting Meets Primary Endpoint of Recurrence-Free SurvivalPrinter Friendly Version
06/02/14One- & Two-Year Survival Rates of 94% and 88% Announced from Phase 1b Trial of Investigational PD-1 Checkpoint Inhibitor Nivolumab and Yervoy® (ipilimumab) in Advanced Melanoma; Ongoing Phase 2/3 Trials to Confirm ResultsPrinter Friendly Version
05/27/14Bristol-Myers Squibb and CytomX Therapeutics Announce Worldwide Collaboration to Develop Probody™ Therapeutics Against Multiple Immuno-Oncology TargetsPrinter Friendly Version
05/27/14Bristol-Myers Squibb and Incyte Enter Clinical Collaboration Agreement to Evaluate Combination Regimen of Two Novel ImmunotherapiesPrinter Friendly Version
05/21/14Bristol-Myers Squibb to Present New Remission Data on ORENCIA® (abatacept) and Clazakizumab at The European League Against Rheumatism (EULAR) 2014 Annual MeetingPrinter Friendly Version
05/19/14Bristol-Myers Squibb and AbbVie Receive U.S. FDA Breakthrough Therapy Designation for Elotuzumab, an Investigational Humanized Monoclonal Antibody for Multiple MyelomaPrinter Friendly Version
05/16/14Bristol-Myers Squibb to Hold Investor Teleconference to Discuss ASCO HighlightsPrinter Friendly Version
05/14/14In Phase 2 and 1b Renal Cell Carcinoma Trials, Investigational PD-1 Immune Checkpoint Inhibitor Nivolumab Showed Antitumor Activity as a Single Agent and in Combination Regimen with Yervoy® (ipilimumab)Printer Friendly Version
05/14/14Bristol-Myers Squibb Announces Two- and Three-Year Survival Data for Nivolumab, an Investigational PD-1 Immune Checkpoint Inhibitor, from Advanced Melanoma Cohort of a Phase 1b StudyPrinter Friendly Version
05/14/14Investigational PD-1 Immune Checkpoint Inhibitor Nivolumab Showed Antitumor Activity in Previously Treated and Chemotherapy-Naïve Patients in Phase 1b Non-Small Cell Lung Cancer TrialsPrinter Friendly Version
05/14/14Investigational PD-1 Immune Checkpoint Inhibitor Nivolumab Receives U.S. FDA Breakthrough Therapy Designation for Hodgkin LymphomaPrinter Friendly Version
05/14/14Bristol-Myers Squibb and Celldex Therapeutics Announce Clinical Trial Collaboration to Evaluate the Combination of Investigational Immunotherapies Nivolumab and VarlilumabPrinter Friendly Version
05/12/14Bristol-Myers Squibb to Present at UBS Global Healthcare ConferencePrinter Friendly Version
05/06/14Bristol-Myers Squibb Announces Retirement of Brian DanielsPrinter Friendly Version
05/05/14Bristol-Myers Squibb Continues to Lead the Advancement of Immuno-Oncology with Broad Set of New Data at 2014 American Society of Clinical Oncology (ASCO) Annual MeetingPrinter Friendly Version
04/29/14Bristol-Myers Squibb Reports First Quarter 2014 Financial ResultsPrinter Friendly Version
04/29/14Bristol-Myers Squibb Acquires iPierian, Inc.Printer Friendly Version
04/24/14Bristol-Myers Squibb Ranks First on 2014 Best Corporate Citizens ListPrinter Friendly Version
04/22/14Bristol-Myers Squibb and Samsung BioLogics Expand Manufacturing AgreementPrinter Friendly Version
04/14/14Bristol-Myers Squibb Submits New Drug Application to U.S. FDA for a Fixed-Dose Combination Tablet of Atazanavir Sulfate with Cobicistat for People Living with HIV-1Printer Friendly Version
04/10/14Bristol-Myers Squibb Presents Phase III Data Demonstrating that Investigational All-oral Daclatasvir and Asunaprevir Therapy Achieved SVR12 Rates of up to 90% Among Broad Range of Genotype 1b Hepatitis C PatientsPrinter Friendly Version
04/07/14Bristol-Myers Squibb Submits NDAs for Daclatasvir and Asunaprevir to US FDA for the Treatment of Hepatitis CPrinter Friendly Version
04/01/14Bristol-Myers Squibb to Announce Results for First Quarter 2014 on April 29Printer Friendly Version
03/24/14Bristol-Myers Squibb to Present Data for Daclatasvir in Multiple Investigational All-oral Combinations across Hepatitis C Genotypes at The International Liver CongressTMPrinter Friendly Version
03/17/14Five Prime Therapeutics and Bristol-Myers Squibb Sign Collaboration Agreement to Discover Novel Immuno-Oncology Therapies for Two Immune Checkpoint PathwaysPrinter Friendly Version
03/05/14Bristol-Myers Squibb Presents Promising Phase IIb Data for Novel, Investigational Attachment Inhibitor for HIV-1 Infected Treatment-Experienced PatientsPrinter Friendly Version
03/03/14Bristol-Myers Squibb Announces DividendPrinter Friendly Version
03/03/14Bristol-Myers Squibb Announces Charitable Donation of $1 Million to Support Immuno-Oncology Education for Patients and CaregiversPrinter Friendly Version
02/24/14Bristol-Myers Squibb Receives U.S. FDA Breakthrough Therapy Designation for All-Oral Daclatasvir Dual Investigational Regimen for Chronic Hepatitis CPrinter Friendly Version
02/21/14In a Subanalysis, Eliquis® (apixaban) Reduced the Risk of Stroke and Demonstrated Fewer Major Bleeding Events versus Warfarin Consistently across Age Groups, Including Older Patients with Nonvalvular Atrial FibrillationPrinter Friendly Version
02/20/14Bristol-Myers Squibb to Present at Cowen and Company 34th Annual Global Health Care ConferencePrinter Friendly Version
02/14/14Bristol-Myers Squibb to Present at Citi 2014 Global Health Care ConferencePrinter Friendly Version
02/05/14Bristol-Myers Squibb to Take Part in Leerink Swann Global Health Care ConferencePrinter Friendly Version
02/03/14Bristol-Myers Squibb Completes Previously Announced Sale of Global Diabetes Business to AstraZenecaPrinter Friendly Version
01/24/14Bristol-Myers Squibb Reports Fourth Quarter and Full Year 2013 Financial ResultsPrinter Friendly Version
01/16/14AstraZeneca and Bristol-Myers Squibb Diabetes Alliance Provides $5 Million Grant for American Diabetes Association's Pathway to Stop Diabetes Research InitiativePrinter Friendly Version
01/13/14U.S. FDA Approves Farxiga™ (Dapagliflozin) Tablets for the Treatment of Adult Patients with Type 2 DiabetesPrinter Friendly Version
01/08/14AstraZeneca and Bristol-Myers Squibb Announce U.S. FDA Approval of Farxiga™ (dapagliflozin)Printer Friendly Version
01/08/14Daclatasvir Marketing Authorization Application for Treatment of Chronic Hepatitis C Validated for Accelerated Regulatory Review by the European Medicines AgencyPrinter Friendly Version
01/06/14Bristol-Myers Squibb to Announce Results for Fourth Quarter, Full Year 2013 on January 24Printer Friendly Version
01/06/14Bristol-Myers Squibb to Present at J.P. Morgan Healthcare ConferencePrinter Friendly Version
01/03/14Bristol-Myers Squibb to Take Part in Goldman Sachs Healthcare CEOs Unscripted ConferencePrinter Friendly Version

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