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Bristol-Myers Squibb (BMY) Announces FDA Approves ts Pomalyst for AIDS-Related and HIV-Negative Kaposi Sarcoma
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U.S. Food and Drug Administration Approves Bristol Myers Squibb’s Pomalyst® (pomalidomide) for AIDS-Related and HIV-Negative Kaposi Sarcoma
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Bristol-Myers Squibb (BMY) Opdivo Plus Yervoy with Limited Chemotherapy Significantly Improves Overall Survival vs. Chemotherapy Alone for Patients with First-Line Metastatic NSCLC in CheckMate -9LA S
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Bristol-Myers Squibb (BMY) Three-Year Data from CheckMate -227 Confirm Durable, Long-Term Survival Benefit for Opdivo Plus Yervoy vs. Chemotherapy in Metastatic First-Line NSCLC
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Bristol Myers Squibb (BMY) and bluebird bio (BLUE) to Present Updated Positive Results from Pivotal KarMMa Study of Ide-cel in R/R Multiple Myeloma Patients at ASCO20
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Bristol Myers Squibb and bluebird bio to Present Updated Positive Results from Pivotal KarMMa Study of Ide-cel in Relapsed and Refractory Multiple Myeloma Patients at ASCO20
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Three-Year Data from CheckMate -227 Confirm Durable, Long-Term Survival Benefit for Opdivo (nivolumab) Plus Yervoy (ipilimumab) vs. Chemotherapy in Metastatic First-Line Non-Small Cell Lung Cancer Pat
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Opdivo (nivolumab) Plus Yervoy (ipilimumab) with Limited Chemotherapy Significantly Improves Overall Survival vs. Chemotherapy Alone for Patients with First-Line Metastatic Non-Small Cell Lung Cancer
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Bristol-Myers Squibb (BMY), bluebird bio (BLUE) Provide Regulatory Update on Idecabtagene Vicleucel for Treatment of Patients with MM, BLA Requires Further Detail
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Bristol Myers Squibb and bluebird bio Provide Regulatory Update on Idecabtagene Vicleucel (ide-cel, bb2121) for the Treatment of Patients with Multiple Myeloma
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GRYT Health and Bristol Myers Squibb Team Up to Launch COVID Advocacy Exchange for Patient Advocates
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Bristol Myers Squibb to Take Part in the UBS Virtual Global Healthcare Conference
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GRYT Health and Bristol Myers Squibb Team Up to Launch COVID Advocacy Exchange for Patient Advocates
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Bristol Myers Squibb Research at ASCO Demonstrates Diverse Approaches in Treating Cancer to Improve Outcomes for Patients
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Bristol Myers Squibb Reports Strong First Quarter 2020 Financial Results
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Bristol-Myers Squibb (BMY) Provides Update on BLA for Lisocabtagene Maraleucel
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Bristol Myers Squibb Provides Update on Biologics License Application (BLA) for Lisocabtagene Maraleucel (liso-cel)
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Bristol-Myers Squibb (BMY) Announces FDA Accepts for Priority Review its Application for CC-486 for Maintenance Treatment of Adult Patients in Remission with AML
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U.S. Food and Drug Administration (FDA) Accepts for Priority Review Bristol Myers Squibb’s Application for CC-486 for Maintenance Treatment of Adult Patients in Remission with Acute Myeloid Leukemia
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Bristol (BMY) and Acceleron (XLRN) Announce Reblozyl Receives Positive CHMP Opinion for Treatment of Adults with Anemia in Beta Thalassemia and Myelodysplastic Syndromes
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Reblozyl (luspatercept) Receives Positive CHMP Opinion for the Treatment of Adults with Anemia in Beta Thalassemia and Myelodysplastic Syndromes
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Press Release Biocartis Group NV: Biocartis Q1 2020 Business Update
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Bristol Myers Squibb (BMY), Exelixis (EXEL) Announce Positive Topline Results from Phase 3 CheckMate -9ER Trial Evaluating Opdivo in Combination with CABOMETYX in Previously Untreated RCC
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Bristol Myers Squibb Announces Positive Topline Result from Pivotal Phase 3 Trial Evaluating Opdivo® (nivolumab) plus Yervoy® (ipilimumab) vs. Chemotherapy in Previously Untreated Malignant Pleural
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Bristol Myers Squibb and Exelixis Announce Positive Topline Results from Pivotal Phase 3 CheckMate -9ER Trial Evaluating Opdivo® (nivolumab) in Combination with CABOMETYX® (cabozantinib) in Previous
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Bristol Myers Squibb Announces Virtual 2020 Annual Meeting of Shareholders
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Intensity Therapeutics Signs Clinical Collaboration Agreement with Bristol Myers Squibb for Advanced Solid Tumors
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Bristol Myers Squibb Announces Acceptance of U.S. and EU Regulatory Filings for Opdivo (nivolumab) Plus Yervoy (ipilimumab) Combined with Limited Chemotherapy in First-Line Lung Cancer
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Bristol Myers Squibb Expands Patient Support Programs to Help Newly Uninsured Patients in the U.S.
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U.S. Food and Drug Administration (FDA) Approves Reblozyl® (luspatercept-aamt), the First and Only Erythroid Maturation Agent, to Treat Anemia in Adults with Lower-Risk Myelodysplastic Syndromes (MDS
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Bristol-Myers Squibb (BMY), bluebird bio (BLUE) Announce Submission of BLA for Anti-BCMA CAR T Cell Therapy Idecabtagene Vicleucel to FDA
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Bristol Myers Squibb and bluebird bio Announce Submission of Biologics License Application (BLA) for Anti-BCMA CAR T Cell Therapy Idecabtagene Vicleucel (Ide-cel, bb2121) to FDA
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Bristol Myers Squibb (BMY) Receives Positive CHMP Opinion Recommending Approval of ZEPOSIA for Treatment of Adult Patients with RRMS with Active Disease
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Bristol Myers Squibb Receives Positive CHMP Opinion Recommending Approval of ZEPOSIA® (ozanimod) for the Treatment of Adult Patients with Relapsing Remitting Multiple Sclerosis with Active Disease
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Bristol-Myers Squibb (BMY) and Acceleron (XLRN) Announces NEJM Publishes Results from Pivotal Phase 3 BELIEVE Trial of Reblozyl in Adult Patients With Beta Thalassemia
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New England Journal of Medicine Publishes Results from Pivotal Phase 3 BELIEVE Trial of Reblozyl (luspatercept-aamt) in Adult Patients With Beta Thalassemia
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Bristol Myers Squibb to Announce Results for First Quarter 2020 on May 7, 2020
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Bristol-Myers Squibb (BMY) Confirms FDA Approved its ZEPOSIA, a New Oral Treatment for Relapsing Forms of MS
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U.S. Food and Drug Administration Approves Bristol Myers Squibb’s ZEPOSIA® (ozanimod), a New Oral Treatment for Relapsing Forms of Multiple Sclerosis
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Bristol-Myers Squibb Postpones April 2, 2020 Investor Day
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Bristol Myers Squibb Appoints Elizabeth Mily as Executive Vice President, Strategy & Business Development
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U.S. Food and Drug Administration Approves Opdivo® (nivolumab) + Yervoy® (ipilimumab) for Patients with Hepatocellular Carcinoma (HCC) Previously Treated with Sorafenib
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Bristol-Myers Squibb (BMY) Highlights Primary Results of ELOQUENT-1 Study Evaluating Empliciti (elotuzumab) Plus Revlimid (lenalidomide) & Dexamethasone
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Bristol Myers Squibb Reports Primary Results of ELOQUENT-1 Study Evaluating Empliciti (elotuzumab) Plus Revlimid (lenalidomide) and Dexamethasone in Patients with Newly Diagnosed, Untreated Multiple M
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Press release Biocartis Group NV: BIOCARTIS ANNOUNCES 2019 RESULTS AND 2020 OUTLOOK
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Biocartis Announces New Immuno-Oncology Project with Bristol-Myers Squibb Aimed at Registration of Idylla™ MSI test in China
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Voluntis and Bristol-Myers Squibb (BMY) to Co-Develop Digital Therapeutics for Oncology
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Voluntis and Bristol-Myers Squibb to Co-Develop Digital Therapeutics for Oncology
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Bristol‑Myers Squibb Announces Dividend Increase
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CORRECTING and REPLACING Bristol‑Myers Squibb Announces Dividend

