Project Details
Description
A Randomized, Double-blind, Vehicle-controlled Multicenter Study to Evaluate the Safety, Tolerability and Efficacy of ATI-50002 Topical Solution Administered Twice-Daily for 3 months in Adult Subjects with Stable Patchy Alopecia Areata
| Status | Finished |
|---|---|
| Effective start/end date | 8/1/17 → 8/30/21 |
Funding
- ACLARIS THERAPEUTICS, INC
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