Prodotti competitors / Area Onco-Ema
FDA grants accelerated approval to talquetamab for relapsed or refractory multiple myeloma
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On August 9, 2023, the Food and Drug Administration granted accelerated approval to talquetamab-tgvs (Talvey, Janssen Biotech, Inc.) adults with relapsed or refractory multiple myeloma who have received at least four prior lines of therapy, including a proteasome inhibitor, an immunomodulatory agent, and an anti-CD38 monoclonal antibody.
View full prescribing information for Talvey
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