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BMS and 2seventy's multiple myeloma therapy Abecma receives expanded FDA approval

BMS and 2seventy's multiple myeloma therapy Abecma receives expanded FDA approval
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FDA approves Abecma as 'earlier line of therapy' for triple-class exposed multiple myeloma

FDA approves Abecma as 'earlier line of therapy' for triple-class exposed multiple myeloma
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FDA Greenlights BMS, J&J CAR-T Therapies for Earlier Multiple Myeloma Treatment

The approvals, third line for BMS and 2seventy Bio’s Abecma and second line for J&J and Legend Biotech’s Carvykti, represent a new class of therapy for these blood cancer patients.

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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: FDA approves Abecma in multiple myeloma -April 05, 2024 at 09:31 am EDT

Bristol Myers Squibb and its partner 2seventy bio announce that the US Food and Drug Administration has approved Abecma for the treatment of adult patients with relapsed or refractory multiple...

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Bristol Myers, 2seventy Bio Get FDA Nod For Abecma For Relapsed Multiple Myeloma Patients

Bristol Myers, 2seventy Bio Get FDA Nod For Abecma For Relapsed Multiple Myeloma Patients
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FDA Approves Abecma for Pretreated R/R Multiple Myeloma

The Food and Drug Administration approved Abecma for adults with relapsed or refractory multiple myeloma who have received two or more previous lines of therapy.

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FDA Approves Ide-Cel for Triple-Class Exposed R/R Multiple Myeloma

The FDA has approved ide-cel (Abecma) for adult patients with relapsed or refractory multiple myeloma after two or more prior lines of therapy.

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Ide-Cel Receives Approval for Earlier Treatment for Relapsed, Refractory Multiple Myeloma

Idecabtagene vicleucel (ide-cel) was able to triple progression-free survival and reduce the risk of disease progression or death in a phase 3 trial.

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