drugset / Trial / NCT04186273

Clinical Safety and Scar Prevention Study of a Topical Antifibrotic Compound FS2.

NCT04186273 ↗

Phase 2 Unknown 50 enrolled University of British Columbia
RandomizedFactorialQuadruple-blindPrevention

Summary

The study will investigate the safety and effectiveness of daily post surgical scar management, using a moisture-balancing base product containing different amounts of a novel (NCE) antifibrogenic compound FS2, a natural metabolite of the kynurenine pathway. Results of recent peer-reviewed, pre-clinical evidence warrant further investigation to validate therapeutic scar preventive efficacy of topically administered/delivered FS2. There are no known safety concerns with current product formulations. Recent Phase I clinical safety and tolerability data further support continuation of the research proposed in this study.

Timeline

Start
2019-12-05
Primary completion
2021-02-01
Completion
2021-03-01

Drugs

EvaluationDrugModalityDoseRoute
Subject FS2 Unknown 0.25 % Topical
Subject FS2 Unknown 0.5 % Topical

Indications