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Bristol-Myers Squibb (BMY) Receives EC Approval for Opdivo Plus Yervoy for Treatment of Mismatch Repair Deficient or Microsatellite Instability–High Metastatic Colorectal Cancer After Prior Chemothe
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Bristol Myers Squibb Receives European Commission Approval for Opdivo (nivolumab) Plus Yervoy (ipilimumab) for the Treatment of Mismatch Repair Deficient or Microsatellite Instability–High Metastati
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Bristol-Myers Squibb (BMY) Receives Positive CHMP Opinion for Opdivo as Adjuvant Treatment for Esophageal or Gastroesophageal Junction Cancer Patients with Residual Pathologic Disease Following Chemor
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Bristol Myers Squibb Receives Positive CHMP Opinion for Opdivo (nivolumab) as Adjuvant Treatment for Esophageal or Gastroesophageal Junction Cancer Patients with Residual Pathologic Disease Following
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Bristol-Myers Squibb (BMY) Receives Positive CHMP Opinion for Anti-BCMA CAR T Cell Therapy Abecm for R/R Multiple Myeloma
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Bristol Myers Squibb Receives Positive CHMP Opinion for Anti-BCMA CAR T Cell Therapy Abecma (idecabtagene vicleucel) for Relapsed and Refractory Multiple Myeloma
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Bristol-Myers Squibb (BMY) Receives European Commission Approval for Onureg as Frontline Oral Maintenance Therapy for Adults with Acute Myeloid Leukemia
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Bristol Myers Squibb Receives European Commission Approval for Onureg® (azacitidine tablets) as Frontline Oral Maintenance Therapy for Adults with Acute Myeloid Leukemia
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Eisai and Bristol Myers Squibb Enter Into Global Strategic Collaboration for Eisai’s MORAb-202 Antibody Drug Conjugate
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Bristol Myers Squibb Announces Dividend
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Exelixis (EXEL) Announces Clinical Trial Collaboration and Supply Agreement with Bristol Myers Squibb (BMY) to Evaluate XL092 in Combination with Immuno-oncology Therapies in Advanced Solid Tumors
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Exelixis Announces Clinical Trial Collaboration and Supply Agreement with Bristol Myers Squibb to Evaluate XL092 in Combination with Immuno-oncology Therapies in Advanced Solid Tumors
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Bristol-Myers Squibb (BMY), Acceleron (XLRN) Present First Results from Phase 2 BEYOND Study of Reblozyl in Adults with NTD Beta Thalassemia
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Bristol Myers Squibb and Acceleron Present First Results from Phase 2 BEYOND Study of Reblozyl® (luspatercept-aamt) in Adults with Non-Transfusion Dependent (NTD) Beta Thalassemia
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Bristol Myers Squibb and GRYT Health Evolve Virtual Patient Advocacy Experience
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Bristol Myers Squibb to Report Results for Second Quarter 2021 on July 28, 2021
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Bristol-Myers Squibb (BMY) Announces Positive Topline Results from Phase 3 TRANSFORM Trial Evaluating Breyanzi Versus Chemotherapy Followed by Stem Cell Transplant in Second-line Relapsed or Refractor
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Bristol Myers Squibb Announces Positive Topline Results from Phase 3 TRANSFORM Trial Evaluating Breyanzi (lisocabtagene maraleucel) Versus Chemotherapy Followed by Stem Cell Transplant in Second-line
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Bristol Myers Squibb to Take Part in Goldman Sachs 42nd Annual Global Healthcare Conference
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Bristol-Myers Squibb (BMY) Presents Data from CheckMate -648 Showing Opdivo plus Chemotherapy and Opdivo plus Yervoy Significantly Improved Overall Survival
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Bristol Myers Squibb Presents Data from CheckMate -648 Showing Opdivo plus Chemotherapy and Opdivo plus Yervoy Significantly Improved Overall Survival Compared to Chemotherapy in Unresectable Advanced
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Bristol-Myers Squibb (BMY) Receives EC Approval for Opdivo Plus Yervoy as First-Line Treatment for Unresectable Malignant Pleural Mesothelioma
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Bristol Myers Squibb Data at EULAR 2021 Highlight Commitment to Driving Advancements Across Multiple Immune-Mediated Rheumatic Diseases
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Bristol Myers Squibb Receives European Commission Approval for Opdivo (nivolumab) Plus Yervoy (ipilimumab) as First-Line Treatment for Unresectable Malignant Pleural Mesothelioma
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Bristol-Myers Squibb (BMY) Announces FDA Approves its Zeposia, an Oral Treatment for Adults with Moderately to Severely Active Ulcerative Colitis
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U.S. Food and Drug Administration Approves Bristol Myers Squibb’s Zeposia® (ozanimod), an Oral Treatment for Adults with Moderately to Severely Active Ulcerative Colitis¹
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Bristol Myers Squibb to Take Part in Bernstein’s 37th Annual Strategic Decisions Conference
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Bristol Myers Squibb to Host Virtual Investor Event to Discuss ASCO 2021 Highlights
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Bristol Myers Squibb Presents New Data at Digestive Disease Week® on Zeposia (ozanimod) Highlighting Clinical Benefits and Safety Profile in Patients with Ulcerative Colitis
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Bristol-Myers Squibb (BMY) Receives Positive CHMP Opinion Recommending Opdivo plus Yervoy for Treatment of Mismatch Repair Deficient or Microsatellite Instability–High Metastatic Colorectal Cancer A
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Bristol Myers Squibb Receives Positive CHMP Opinion Recommending Opdivo (nivolumab) plus Yervoy (ipilimumab) for Treatment of Mismatch Repair Deficient or Microsatellite Instability–High Metastatic
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Bristol-Myers Squibb (BMY) Announces FDA Approval for Opdivo as Adjuvant Treatment for GEJ Cancer
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U.S. Food and Drug Administration Approves Opdivo® (nivolumab) as Adjuvant Treatment of Completely Resected Esophageal or Gastroesophageal Junction Cancer in Patients who have Received Neoadjuvant Ch
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Bristol-Myers Squibb (BMY) Elects Manuel Hidalgo Medina, M.D., Ph.D. to Board of Directors
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Bristol Myers Squibb Elects Manuel Hidalgo Medina, M.D., Ph.D. to Board of Directors
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Bristol Myers Squibb Announces LAG-3-Blocking Antibody Relatlimab and Nivolumab Fixed-Dose Combination Significantly Improves Progression-Free Survival vs. Opdivo (nivolumab) in Patients with Previous
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Six-and-a-Half-Year Outcomes for Opdivo (nivolumab) in Combination with Yervoy (ipilimumab) Continue to Demonstrate Durable Long-Term Survival Benefits in Patients with Advanced Melanoma
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Opdivo (nivolumab) Plus Yervoy (ipilimumab) with Two Cycles of Chemotherapy Demonstrates Durable Overall Survival vs. Chemotherapy at Two Years in First-Line Non-Small Cell Lung Cancer in Phase 3 Chec
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Four-Year Data from Phase 3 CheckMate -227 Trial Show Durable, Long-Term Survival with Opdivo (nivolumab) Plus Yervoy (ipilimumab) in Patients with Non-Small Cell Lung Cancer with PD-L1 Expression ≥
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Long-Term Data from Pivotal KarMMa Study Continue to Demonstrate Deep and Durable Responses and Predictable Safety Profile with Bristol Myers Squibb and bluebird bio’s Abecma (idecabtagene vicleucel
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Exscientia announces multi-target, AI-driven drug discovery collaboration with Bristol Myers Squibb
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Agenus (AGEN) and Bristol Myers Squibb (BMY) Announce Exclusive Global License for Agenus' Anti-TIGIT Bispecific Antibody Program
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Agenus and Bristol Myers Squibb Announce Exclusive Global License for Agenus’ Anti-TIGIT Bispecific Antibody Program
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Agenus and Bristol Myers Squibb Announce Exclusive Global License for Agenus’ Anti-TIGIT Bispecific Antibody Program
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Agenus and Bristol Myers Squibb Announce Exclusive Global License for Agenus’ Anti-TIGIT Bispecific Antibody Program
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Bristol Myers Squibb to Take Part in UBS Global Healthcare Virtual Conference
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Bristol Myers Squibb Presents Late-Breaking Phase 3 Data Demonstrating Health Status Benefits of Mavacamten in Patients with Obstructive Hypertrophic Cardiomyopathy at American College of Cardiology�
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Bristol Myers Squibb (BMY) Presents New Research at ASCO and EHA 2021 Featuring Novel Approaches and Demonstrating Significant Progress to Improve Survival in Cancer and Blood Disorders
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Bristol Myers Squibb Presents New Research at ASCO and EHA 2021 Featuring Novel Approaches and Demonstrating Significant Progress to Improve Survival in Cancer and Blood Disorders
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Bristol Myers Squibb to Take Part in the 2021 Bank of America Securities Health Care Conference

