drugset / Trial / NCT00680095
Summary
The purpose of this study is to determine the cumulative irritation potential of the products listed by the Sponsor.
Timeline
- Start
- 2007-01-22
- Primary completion
- 2007-02-19
- Completion
- 2007-02-19
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Sodium Lauryl Sulfate | Small molecule | 0.5 % | Topical |
| Subject | Tavaborole | Small molecule | 2.5 % | Topical |
| Subject | Tavaborole | Small molecule | 5 % | Topical |
| Subject | Tavaborole | Small molecule | 7.5 % | Topical |