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EMA approval · 2024-10-11

EMA Authorised: Halaven (Eribulin) — Eisai GmbH

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Summary

The EMA authorised Halaven (eribulin) for breast neoplasms and liposarcoma under Eisai GmbH, with a decision date of 26 July 2024.

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Diseases / indications

Drugs mentioned

  • Halaven (eribulin)

Snippet

Status: Authorised. Therapeutic area: Breast Neoplasms;Liposarcoma. MAH: Eisai GmbH. Decision date: 26/07/2024