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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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FDA Grants Full Approval for TIVDAK® to Treat Recurrent or Metastatic Cervical Cancer

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

Company Announcement Full approval based on global Phase 3 study demonstrating overall survival benefit of TIVDAK compared to chemotherapyTIVDAK is the first antibody-drug conjugate in this patient.

Genmab A/S: TIVDAK (tisotumab vedotin-tftv) Receives U S FDA Approval to Treat Recurrent or Metastatic Cervical Cancer

Genmab A/S: TIVDAK (tisotumab vedotin-tftv) Receives U S FDA Approval to Treat Recurrent or Metastatic Cervical Cancer
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