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EMA Product

Mektovi

Product approved by European Medicines Agency (EU)

Basic Information

Mektovi

Regulatory Information

EMEA/H/C/004579

Authorised

September 20, 2018

11

December 10, 2024

Company Information

France

Les Cauquillous 81500 - Lavaur

PIERRE FABRE MEDICAMENT

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Melanoma Binimetinib in combination with encorafenib is indicated for the treatment of adult patients with unresectable or metastatic melanoma with a BRAF V600 mutation. Non-small cell lung cancer (NSCLC) Binimetinib in combination with encorafenib is indicated for the treatment of adult patients with advanced non-small cell lung cancer with a BRAF V600E mutation.

Overview Summary

Mektovi is a medicine used in adults for treating certain cancers when their cells have a mutation (change) in their genes called 'BRAF V600'. Mektovi is used in combination with another medicine, encorafenib , to treat: - melanoma (a skin cancer) that has spread or cannot be removed by surgery; - a type of lung cancer called non-small cell lung cancer (NSCLC). It is used when the cancer is advanced and has the BRAF V600E version of the mutation. Mektovi contains the active substance binimetinib.

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