FDA
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2seventy bio Reports Preliminary* Full-Year U.S. Abecma Sales and Select Financial Results
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2seventy bio to Report Second Quarter 2024 Financial Results on August 7, 2024
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U.S. FDA Approves Bristol Myers Squibb (BMY) and 2seventy bio’s (TSVT) Abecma for Triple-Class Exposed Relapsed or Refractory Multiple Myeloma After Two Prior Lines of Therapy
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Bristol-Myers Squibb (BMY): FDA Advisers Vote 8:3 in Favor of Abecma as Earlier Treatment for a Type of Blood Cancer
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Bristol Myers Squibb and 2seventy bio Share Update on U.S. FDA Oncologic Drugs Advisory Committee Meeting for Abecma in Triple-Class Exposed Multiple Myeloma Based on KarMMa-3 Study
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2seventy bio to Host Investor Call at 8:00am ET on Tuesday, December 12 to Discuss Data from KarMMa-3 and KarMMa-2 Studies of Abecma (idecabtagene vicleucel)
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2seventy bio to lay off 40% of workforce; CEO to step down
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