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TIVDAK® (tisotumab vedotin-tftv) Receives U.S. FDA Approval to Treat Recurrent or Metastatic Cervical Cancer

TIVDAK® (tisotumab vedotin-tftv) Receives U.S. FDA Approval to Treat Recurrent or Metastatic Cervical Cancer
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Pfizer's TIVDAK® Receives Full FDA Approval for Treating Recurrent or Metastatic Cervical Cancer – India Education | Latest Education News | Global Educational News

Pfizer Inc. (NYSE: PFE) and Genmab A/S (Nasdaq: GMAB) today announced the U.S. Food and Drug Administration (FDA) approves the supplemental Biologics License Application (sBLA) granting full approval for TIVDAK® (tisotumab vedotin-tftv) for the treat ....

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FDA Fully Approves TIVDAK for Recurrent, Metastatic Cervical Cancer

FDA Fully Approves TIVDAK for Recurrent, Metastatic Cervical Cancer
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Tisotumab Vedotin Gains Full FDA Approval for Recurrent or Metastatic Cervical Cancer

The FDA granted full approval for tisotumab vedotin-tftv to treat recurrent or metastatic cervical cancer that progressed after chemotherapy, offering patients improved overall survival and a manageable safety profile. ....

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FDA Grants Full Approval to Tisotumab Vedotin-tftv for Recurrent, Metastatic Cervical Cancer

Tisotumab vedotin-tftv is the first antibody-drug conjugate to demonstrate positive overall survival data in patients with previously treated recurrent or metastatic cancer. ....

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