This is a randomized, double-blind, placebo-controlled, parallel-group phase 1b study to evaluate AT193 in approximately 44 participants with HS. The treatment period will be 8 weeks followed by a 2-week nontreatment follow-up. The primary objective of this study is to evaluate the safety and tolerability of AT193. The secondary objectives of this study are to evaluate the preliminary efficacy in the treatment of HS.
| Condition | Hidradenitis Suppurativa |
|---|---|
| Treatment | AT193 |
| Clinical Study Identifier | NCT04989517 |
| Sponsor | Azora Therapeutics Australia Pty Ltd |
| Last Modified on | 2 July 2022 |
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