Prognia
Drug Database
🇪🇺EU · EMAAuthorisedATC: L01XE38

Cotellic(cobimetinib hemifumarate)

Melanoma

Marketing Authorisation Holder: Roche Registration GmbH

EMA Authorisation: 20/11/2015

INN: cobimetinib

Indication

Cotellic is indicated for use in combination with vemurafenib for the treatment of adult patients with unresectable or metastatic melanoma with a BRAF V600 mutation.

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.