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U.S. FDA Approves Bristol Myers Squibb and 2seventy bio's Abecma for Triple-Class Exposed Relapsed or Refractory Multiple Myeloma After Two Prior Lines of Therapy -April 05, 2024 at 09:08 am EDT

Abecma tripled progression-free survival compared to standard regimens in the Phase 3 KarMMa-3 trial, with a 51% reduction in risk of disease progression or death and a well-established safety...

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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

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, 2seventy bio receive FDA approval for Abecma to treat multiple myeloma

Bristol Myers, 2seventy bio receive FDA approval for Abecma to treat multiple myeloma
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FDA Approves Bristol-Myers/2seventy Bio's Abecma For Earlier Use In Pretreated Blood Cancer Patients With Updated Boxed Warning On Secondary Cancer - 2seventy bio (NASDAQ:TSVT), Bristol-Myers Squibb (NYSE:BMY)

FDA Approves Bristol-Myers/2seventy Bio's Abecma For Earlier Use In Pretreated Blood Cancer Patients With Updated Boxed Warning On Secondary Cancer - 2seventy bio (NASDAQ:TSVT), Bristol-Myers Squibb (NYSE:BMY)
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Bristol Myers Wins FDA Nod For Abecma

Bristol Myers Wins FDA Nod For Abecma
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