Prognia
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🇪🇺EU · EMAAuthorisedATC: L01FX26Orphan Medicine

Elahere(mirvetuximab soravtansine)

Ovarian Neoplasms;Fallopian Tube Neoplasms;Peritoneal Neoplasms

Marketing Authorisation Holder: AbbVie Deutschland GmbH & Co. KG

EMA Authorisation: 14/11/2024

INN: mirvetuximab soravtansine

Indication

Elahere as monotherapy is indicated for the treatment of adult patients with folate receptor-alpha (FRα) positive, platinum-resistant high grade serous epithelial ovarian, fallopian tube, or primary peritoneal cancer who have received one to three prior systemic treatment regimens.

Official EMA Resources

View on EMA (ema.europa.eu)

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Medical disclaimer: This information is intended for qualified healthcare professionals. Always verify with the official EMA Summary of Product Characteristics (SmPC) before clinical use.