FDA Approves Idecabtagene vicleucel for Relapsed or Refractory Multiple Myeloma

On April 4, the US Food and Drug Administration (FDA) approved idecabtagene vicleucel for the treatment of adult patients with relapsed or refractory multiple myeloma after 2 or more prior lines of therapy including an immunomodulatory agent, a proteasome inhibitor, and an anti-CD38 monoclonal antibody. 

For more information read the Bristol Myers Squibb announcement.

Posted 4/9/2024