BL 761208
BL 761208
U.S. License Holder:
Seagen
Date of License:
September-20-2021
Last Update:
Nov-15-2024
FDA-Approved IndicationsTIVDAK (tisotumab vedotin-tftv) is a tissue factor-directed antibody and microtubule inhibitor conjugate indicated for the treatment of adult patients with recurrent or metastatic cervical cancer with disease progression on or after chemotherapy.
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