Abecma® (idecabtagene vicleucel)

BL 125736

Abecma® (idecabtagene vicleucel)

BL 125736

U.S. License Holder:

Celgene Corp. / Bristol-Myers Squibb

Date of License:

March-26-2021

Last Update:

Nov-15-2024

approved_indications FDA-Approved Indications

ABECMA (idecabtagene vicleucel) is a B-cell maturation antigen (BCMA)-directed genetically modified autologous T cell immunotherapy indicated for the treatment of adult patients with relapsed or refractory multiple myeloma after four or more prior lines of therapy, including an immunomodulatory agent, a proteasome inhibitor, and an anti-CD38 monoclonal antibody.

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Methodology

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