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FDA approves Abecma for relapsed, refractory multiple myeloma

FDA approves Abecma for relapsed, refractory multiple myeloma
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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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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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FDA Approves Idecabtagene Vicleucel for Multiple Myeloma After 2 or More Lines of Therapy

The approval expands the prior indication of idecabtagene vicleucel (Abecma; Bristol Myers Squibb), which will make the drug available to patients in earlier lines.

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Older, Younger Patients With MM Show Similar Outcomes With Teclistamab

Real-world data presented at the 2023 American Society of Hematology Annual Meeting and Exposition showed similar toxicity profiles and outcomes among older and younger patients with multiple myeloma (MM) treated with teclistamab.

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New Study Reveals Global Disparities in Access to Multiple Myeloma Cell Therapies

“Unfortunately, limited access to these therapies worldwide appears to be a major challenge,” the researchers wrote.

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