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EMA approval · 2026-06-05

EMA Authorised: Tivdak (tisotumab vedotin) — Genmab A/S

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Summary

EMA authorised Tivdak (tisotumab vedotin) for uterine cervical neoplasms, expanding treatment options in this indication.

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Diseases / indications

Drugs mentioned

  • TIVDAK (tisotumab vedotin)

Snippet

Status: Authorised. Therapeutic area: Uterine Cervical Neoplasms. MAH: Genmab A/S. Decision date: 02/06/2026