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🇪🇺EU · EMAAuthorisedATC: L01Orphan Medicine

Abecma(idecabtagene vicleucel)

Multiple Myeloma

Marketing Authorisation Holder: Bristol-Myers Squibb Pharma EEIG

EMA Authorisation: 18/08/2021

INN: idecabtagene vicleucel

Indication

Abecma is indicated for the treatment of adult patients with relapsed and refractory multiple myeloma who have received at least two prior therapies, including an immunomodulatory agent, a proteasome inhibitor and an anti CD38 antibody and have demonstrated disease progression on the last therapy.

Official EMA Resources

View on EMA (ema.europa.eu)

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Medical disclaimer: This information is intended for qualified healthcare professionals. Always verify with the official EMA Summary of Product Characteristics (SmPC) before clinical use.