
Pfizer Inc., based in New York, recently announced that the US Food and Drug Administration (FDA) has approved BRAFTOVI (encorafenib) + MEKTOVI (binimetinib) for the treatment of adult patients with metastatic non-small cell lung cancer (NSCLC) harboring a BRAF V600E mutation. This approval is based on positive results from the ongoing Phase 2 PHAROS clinical trial. The study demonstrated the efficacy of the BRAFTOVI + MEKTOVI combination therapy, with significant response rates and durations observed in both treatment-naive and previously treated patients.
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