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FDA Approves Encorafenib + Binimetinib for NSCLC with a BRAF V600E Mutation

On October 11, the US Food and Drug Administration (FDA) approved encorafenib in combination with binimetinib for adult patients with metastatic non-small cell lung cancer (NSCLC) with a BRAF V600E mutation, as detected by an FDA-approved test.

For more information read the FDA announcement and the Pfizer announcement

Posted 10/12/2023