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Clinical Trial Summary

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


Clinical Trial Description

Dose Escalation (Part 1): To evaluate safety, pharmacokinetics, pharmacodynamics of FORE8394 in adult and pediatric patients with advanced BRAF- mutated tumors, and to identify the recommended Phase 2 Dose. Dose Extension (Part 2): To access objective tumor response to FORE8394 treatment in adult and in adolescent patients with advanced BRAF- mutated tumors, to access RECIST, and to access pharmacokinetics, pharmacodynamics, and safety. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02428712
Study type Interventional
Source Fore Biotherapeutics
Contact
Status Active, not recruiting
Phase Phase 1/Phase 2
Start date April 2015
Completion date December 2024

See also
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