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Cervical Cancer: Seagen & Genmab Granted FDA Accelerated Approval

Cervical Cancer: Seagen & Genmab Granted FDA Accelerated Approval

Sep 21, 2021 | News, Regulatory

The US FDA (Food and Drug Administration) has granted Seagen and Genmab accelerated approval for TIVDAK (tisotumab vedotin-tftv) to treat adult patients with recurring or metastatic cervical cancer who have previously received disease progression or chemotherapy....

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