Project Details
Description
A Randomized, Double-Blind, Placebo-Controlled Multicenter Study to Evaluate the Safety, Tolerability and Efficacy of ATI-501 Oral Suspension Compared to Placebo in Adult Subjects with Alopecia Areata, Alopecia Universalis or Alopecia Totalis
| Status | Finished |
|---|---|
| Effective start/end date | 6/15/18 → 6/30/22 |
Funding
- ACLARIS THERAPEUTICS, INC
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