30 August 2024 - European approval is based on results from the Phase 2 PHAROS trial, which showed a meaningful clinical benefit to BRAF V600E mutated advanced non-small cell lung cancer patients with an objective response rate of 75% in treatment naïve patients and 46% in previously treated patients.
Pierre Fabre Laboratories announced today that the European Commission has approved Braftovi (encorafenib) in combination with Mektovi (binimetinib) for the treatment of adult patients with advanced non-small cell lung cancer with a BRAF V600E mutation.