Prognia
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🇪🇺EU · EMAAuthorisedConditional Approval

Elrexfio(elranatamab)

Multiple Myeloma

Marketing Authorisation Holder: Pfizer Europe MA EEIG

EMA Authorisation: 07/12/2023

INN: elranatamab

Indication

Elrexfio is indicated as monotherapy for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least three 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.