FDA approves tisotumab vedotin-tftv for recurrent or metastatic cervical cancer

FDA

29 April 2024 - Today, the FDA granted traditional approval to tisotumab vedotin-tftv (Tivdak, Seagen) for recurrent or metastatic cervical cancer with disease progression on or after chemotherapy. 

Tisotumab vedotin-tftv previously received accelerated approval for this indication.

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Michael Wonder

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Michael Wonder

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Cancer , Outcome , Medicine , US