Therapeutic Response

BRAF p.V600K status confers therapeutic sensitivity to Dabrafenib in patients with Melanoma.

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Statements

Source and description
Tafinlar (dabrafenib) [product information]. EMA.

The European Medicines Agency (EMA) has authorized dabrafenib as a monotherapy or in combination with trametinib for the treatment of adult patients with unresectable or metastatic melanoma with a BRAF V600 variant.

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