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Bristol Myers Squibb Receives European Commission Approval for Opdivo® (nivolumab) in Combination with Cisplatin and Gemcitabine for the First-Line Treatment of Adult Patients with Unresectable or Metastatic Urothelial Carcinoma

Approval based on results from CheckMate -901, the first Phase 3 trial in this patient population with an immunotherapy-chemotherapy combination to demonstrate survival benefit versus. ....

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Bristol Myers Squibb to Present Data at ASCO & EHA from More Than 130 Studies Across 25 Diseases Supporting Expansion into New Indications, Demonstrating Long-Term Survival, and Highlighting Novel Modalities and Research Platforms

Bristol Myers Squibb (NYSE: BMY) today announced the presentation of data across its oncology and hematology portfolio at the upcoming 2024 American Society of Clinical Oncology (ASCO) Annual Meeting ....

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Bristol Myers Squibb Provides Update on Phase 3 CheckMate -73L Trial

Bristol Myers Squibb Provides Update on Phase 3 CheckMate -73L Trial
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Orchard Therapeutics Announces Multiple Presentations at ASGCT 2024

Orchard Therapeutics Announces Multiple Presentations at ASGCT 2024
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