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BMY

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 13:42:22 2024-06-27 EDT 		5-day change 1st Jan Change
41.84 USD +1.61% Intraday chart for Bristol-Myers Squibb Company +0.64% -19.81%
02:32pm Purple Biotech Says Interim Data from Pancreatic Cancer Drug Study Shows Promise MT
06-26 2seventy bio Sells Hemophilia A Candidate, Gene Editing Technology to Novo Nordisk; Shares Rise After Hours MT

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Purple Biotech Says Interim Data from Pancreatic Cancer Drug Study Shows Promise
2seventy bio Sells Hemophilia A Candidate, Gene Editing Technology to Novo Nordisk; Shares Rise After Hours
Top Midday Stories: Southwest Cuts Q2 Guidance; HHS to Lower Costs for Medicare Enrollees on 64 Drugs; Bosch Weighing Acquisition Offer for Whirlpool; Novo Nordisk to Record $816.2 Million Impairment
Biden Administration to Lower Costs for 64 Prescription Drugs for Medicare Enrollees
Biden Administration to Lower Costs for 64 Prescription Drugs for Medicare Enrollees
Bristol Myers : approbation accélérée en cancer colorectal
Bristol Myers Squibb Announces U.S. FDA Accelerated Approval of KRAZATI®? in Combination with Cetuximab for Adult Patients with Previously Treated KRAS G12C-Mutated Locally Advanced or Metastatic Colorectal Cancer
Bristol-Myers Squibb's Colorectal Cancer Therapy Receives FDA Approval
US FDA approves Bristol Myers' colorectal cancer therapy
Bristol-Myers Squibb Says EMA Validates Application for Subcutaneous Opdivo
Bristol Myers : demande validée pour Opdivo sous-cutané
Bristol Myers Squibb Announces European Medicines Agency Validates Extension Application to Introduce New Route of Administration (Subcutaneous Use) for Opdivo
Bristol Myers : l'ex-CEO d'Agilent rejoint le conseil
Bristol Myers Squibb Appoints Michael R. McMullen as Independent Director and Member of the Audit Committee, Effective July 1, 2024
Immunocore Randomizes First Patient in Phase 3 Trial of Cutaneous Melanoma Combination Treatment
Bristol Myers : dividendes décidés par le conseil
Bristol Myers Squibb Declares A Quarterly Dividend, Payable on August 1, 2024
Bristol Myers : approbation de la FDA pour un traitement
Bristol-Myers Squibb's Augtyro Gets FDA Accelerated Approval for Treatment of Solid Tumors
Bristol Myers Squibb Announces U.S. Food and Drug Administration Approves Augtyro (repotrectinib) for the Treatment of Patients with NTRK-Positive Locally Advanced or Metastatic Solid Tumors
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