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EMA recommends approval of CAR-T cell therapy for relapsed and refractory multiple myeloma

Pavankumar Kamat   |   Clinical Summary   |   31 March 2022
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Takeaway

  • The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has recommended granting conditional marketing authorization for ciltacabtagene autoleucel, a new gene therapy for relapsed and refractory multiple myeloma (R/R MM).

Why this matters

  • Ciltacabtagene autoleucel is a chimeric antigen receptor (CAR)-T cell drug...

          

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