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🇪🇺EU · EMAAuthorisedATC: L01FX35

Datroway(datopotamab deruxtecan)

Breast Neoplasms

Marketing Authorisation Holder: Daiichi Sankyo Europe GmbH

EMA Authorisation: 04/04/2025

INN: datopotamab deruxtecan

Indication

Breast cancerDatroway as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic hormone receptor (HR)-positive, HER2-negative breast cancer who have received endocrine therapy and at least one line of chemotherapy in the advanced setting.

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.