drugset / Trial / NCT05503797

A Study to Assess the Efficacy and Safety of FORE8394 in Participants With Cancer Harboring BRAF Alterations

NCT05503797

Phase 2 Recruiting 254 enrolled Fore Biotherapeutics
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The objective of this Master Protocol is to evaluate the efficacy and safety of plixorafenib in participants with locally advanced or metastatic solid tumors, or recurrent or progressive primary central nervous system (CNS) tumors harboring BRAF fusions, or in participants with rare BRAF V600-mutated solid tumors, melanoma, thyroid, or recurrent primary CNS tumors.

Timeline

Start
2023-02-21
Primary completion
2026-06-27
Completion
2026-12-28

Drugs

EvaluationDrugModalityDoseRoute
Subject Plixorafenib Small molecule Oral