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Bristol-Myers Squibb (BMY) Reports Positive CHMP Opinion for Once-Daily Sotyktu
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Bristol Myers Squibb Announces Positive CHMP Opinion for Once-Daily Sotyktu (deucravacitinib) as a Treatment for Adults With Moderate-to-Severe Plaque Psoriasis
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Bristol-Myers Squibb (BMY) Reports TRANSCEND CLL 004 Trial of Breyanzi Met Primary Endpoint
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Bristol Myers Squibb Announces TRANSCEND CLL 004 Trial of Breyanzi® (lisocabtagene maraleucel) Met Primary Endpoint of Complete Response Rate in Patients with Relapsed or Refractory Chronic Lymphocyt
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Bristol Myers Squibb to Present at J.P. Morgan’s 41st Annual Healthcare Conference
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Bristol-Myers Squibb (BMY) completes sale of Syracuse, New York manufacturing facility
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Bristol Myers Squibb Completes Sale of Manufacturing Facility in Syracuse, New York
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Evotec Achieves Further Progress in Neuroscience Collaboration with Bristol Myers Squibb
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Bristol Myers Squibb to Report Results for Fourth Quarter 2022 on February 2, 2023
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Bristol Myers Squibb Announces First Disclosures and New Data at ASH 2022, Demonstrating Commitment to Raising Standards in Treatment Through Broad Multiple Myeloma Portfolio
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Bristol Myers Squibb Announces Dividend Increase
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Envisagenics Announces Research Collaboration with Bristol Myers Squibb
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Bristol Myers Squibb to Participate in the Wolfe Research Healthcare Conference
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Data Reinforcing Impact of Bristol Myers Squibb Cardiovascular Portfolio to be Presented at American Heart Association Scientific Sessions 2022
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Bristol-Myers Squibb (BMY) Announces Phase 3 COMMANDS Trial Met its Primary Endpoint
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Bristol Myers Squibb Announces Positive Topline Results of Phase 3 COMMANDS Trial
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Bristol-Myers Squibb (BMY) Extends Multi-Year Deal with Obsidian Therapeutics
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Obsidian Therapeutics Announces Extension of Multi-Year Collaboration Agreement with Bristol Myers Squibb
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Bristol-Myers Squibb (BMY) Reports Q3 Revenue of $11.22B, EPS of $1.99
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Bristol-Myers Squibb (BMY) Reports New Zeposia Data Shows COVID-19 Outcomes and Preservation of Long-Term Cognitive Function from Separate Analyses in Patients with Relapsing Forms of Multiple Scleros
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New Zeposia (ozanimod) Data Highlight COVID-19 Outcomes and Preservation of Long-Term Cognitive Function from Separate Analyses in Patients with Relapsing Forms of Multiple Sclerosis
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Bristol Myers Squibb Reports Third Quarter Financial Results for 2022
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Bristol-Myers Squibb (BMY) Reports New Data Showing Continuous Zeposia (ozanimod) Treatment Prevents Disease Relapse Over One Year in 86.1% of Patients Who Respond at the End of the Induction Period
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New Data Presented at the American College of Gastroenterology Annual Scientific Meeting Demonstrate Continuous Zeposia (ozanimod) Treatment Prevents Disease Relapse Over One Year in 86.1% of Patients
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Bristol-Myers Squibb (BMY) Announces FDA Accepts sNDA for CAMZYOS in Symptomatic Obstructive Hypertrophic Cardiomyopathy to Reduce the Need for Septal Reduction Therapy
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U.S. Food and Drug Administration (FDA) Accepts Supplemental New Drug Application for CAMZYOS® (mavacamten) in Symptomatic Obstructive Hypertrophic Cardiomyopathy to Reduce the Need for Septal Reduct
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Bristol Myers Squibb Presents Data from CheckMate -76K Showing Opdivo (nivolumab) Reduced the Risk of Recurrence or Death by 58% Versus Placebo in Patients with Completely Resected Stage IIB or IIC Me
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Bristol Myers Squibb Announces Change to Earnings Conference Call Dial-In Information for Third Quarter 2022 Results Scheduled for October 26, 2022
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Exelixis (EXEL) Expands Clinical Trial Collaboration and Supply Agreement with Bristol Myers Squibb (BMY)
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Exelixis Expands Clinical Trial Collaboration and Supply Agreement with Bristol Myers Squibb to Include the Fixed-Dose Combination of Nivolumab and Relatlimab in Combination with XL092 in Phase 1b STE
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Bristol-Myers Squibb (BMY) Granted EU Approval of Opdualag
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Bristol Myers Squibb Receives European Commission Approval for LAG-3-Blocking Antibody Combination, Opdualag (nivolumab and relatlimab), for the Treatment of Unresectable or Metastatic Melanoma with T
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Bristol-Myers Squibb (BMY) Reports Adjuvant Treatment with Opdivo Demonstrated Statistically Significant and Clinically Meaningful Improvement in Recurrence-Free Survival (RFS) in Patients with Stage
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Bristol Myers Squibb Announces Adjuvant Treatment with Opdivo (nivolumab) Demonstrated Statistically Significant and Clinically Meaningful Improvement in Recurrence-Free Survival (RFS) in Patients wit
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Bristol Myers Squibb Announces Dividend
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Bristol-Myers Squibb (BMY) Announces FDA Approval for Sotyktu to Treat Moderate-to-Severe Plaque Psoriasis
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Bristol-Myers Squibb (BMY) Reports Strong New Sotyktu Data
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Bristol Myers Squibb Announces New Sotyktu™ (deucravacitinib) Long-Term Data Showing Clinical Efficacy Maintained for Up to Two Years with Continuous Treatment in Moderate-to-Severe Plaque Psoriasis
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U.S. Food and Drug Administration Approves Sotyktu™ (deucravacitinib), Oral Treatment for Adults with Moderate-to-Severe Plaque Psoriasis
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Bristol Myers Squibb Employees to Relay Nearly 3,000 Miles Cross-Country Aspiring to Raise Over $1 Million for the V Foundation for Cancer Research
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Bristol Myers Squibb to Report Results for Third Quarter 2022 on October 26, 2022
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Bristol Myers Squibb to Participate in the Morgan Stanley 20th Annual Global Healthcare Conference
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Bristol Myers Squibb Research at ESMO Congress 2022 Highlights Depth of Development Program Across Early- and Late-Stages of Cancer
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Bristol Myers Squibb to Participate in Citi’s 17th Annual BioPharma Conference
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Late-Breaking Results From Phase 2 AXIOMATIC-SSP Study of Milvexian, an Investigational Oral Factor XIa Inhibitor, Show Favorable Antithrombotic Profile in Combination With Dual Antiplatelet Therapy
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Bristol-Myers Squibb (BMY) Completes Acquisition of Turning Point Therapeutics (TPRX)
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Bristol Myers Squibb Completes Acquisition of Turning Point Therapeutics, Expanding Precision Oncology Portfolio
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Bristol-Myers Squibb (BMY), Turning Point Therapeutics (TPRX) Announce Expiration of HSR Act Waiting Period and Clearance from Federal Cartel Office of Germany Related to Pending Acquisition
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Bristol Myers Squibb and Turning Point Therapeutics Announce Expiration of HSR Act Waiting Period and Clearance from Federal Cartel Office of Germany Related to Pending Acquisition of Turning Point Th
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Big Short's Burry Liquidates ~$200M in Long Stock Bets, Now Has Just One Stock

