drugset / Trial / NCT02428712

A Study of FORE8394 as a Single Agent in Patients With Advanced Unresectable Solid Tumors

NCT02428712

Phase 1/2 Completed 113 enrolled Fore Biotherapeutics
NaSingle-groupOpen-labelTreatment

Summary

The objective of this study is to determine the safety, pharmacokinetics, maximum tolerated dose/recommended Phase 2 dose, and efficacy of FORE8394.

Timeline

Start
2015-04
Primary completion
2024-07-12
Completion
2024-07-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Plixorafenib Small molecule

Indications

No indication recorded.