GSK receives EU approval for Mekinist for melanoma

4 July 2014

The European Commission has granted marketing authorization for UK pharma giant GlaxoSmithKline’s (LSE: GSK) Mekinist(trametinib) as a single agent in the treatment of adult patients with unresectable or metastatic melanoma with a BRAF V600 mutation.

Trametinib has not demonstrated clinical activity in patients who have progressed on a prior BRAF inhibitor therapy. Before taking trametinib, patients must have confirmation of a BRAF V600 mutation using a validated test.

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