FDA Approves Therapy for Metastatic Cervical Cancer

The US Food and Drug Administration recently granted approval to tisotumab vedotin-tftv (Tivdak, Seagen Inc. [now a part of Pfizer Inc.]) for the treatment of recurrent or metastatic cervical cancer with disease progression on or after chemotherapy. The traditional approval comes after tisotumab vedotin-tftv was given accelerated approval for this indication.

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