Prognia
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🇪🇺EU · EMAAuthorisedATC: L01EK03

Fotivda(tivozanib)

Carcinoma, Renal Cell

Marketing Authorisation Holder: Recordati Netherlands B.V.

EMA Authorisation: 24/08/2017

INN: tivozanib hydrochloride monohydrate

Indication

Fotivda is indicated for the first line treatment of adult patients with advanced renal cell carcinoma (RCC) and for adult patients who are VEGFR and mTOR pathway inhibitor-naïve following disease progression after one prior treatment with cytokine therapy for advanced RCC. Treatment of advanced renal cell carcinoma.

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.