medwireNews: The EMA’s Committee for Medicinal Products for Human Use has recommended marketing authorization be given for the combination of encorafenib and binimetinib in patients with BRAF V600-mutated unresectable or metastatic melanoma.
The efficacy of the combined BRAF inhibitor and the MEK inhibitor regimen in this population was demonstrated by overall survival findings from the COLUMBUS trial .
The joint therapy has also been approved by the US FDA for this indication.
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