Prognia
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🇪🇺EU · EMAWithdrawnATC: L01EX23Conditional Approval

Gavreto(pralsetinib)

Carcinoma, Non-Small-Cell Lung

Marketing Authorisation Holder: Blueprint Medicines (Netherlands) B.V.

EMA Authorisation: 18/11/2021

INN: pralsetinib

Indication

Gavreto is indicated as monotherapy for the treatment of adult patients with rearranged during transfection (RET) fusion-positive advanced non-small cell lung cancer (NSCLC) not previously treated with a RET inhibitor.

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.