drugset / Trial / NCT04186273
Clinical Safety and Scar Prevention Study of a Topical Antifibrotic Compound FS2.
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | FS2 | Unknown | 0.25 % | Topical |
| Subject | FS2 | Unknown | 0.5 % | Topical |