drugset / Trial / NCT06345404

Safety, Tolerability, and Preliminary Efficacy of Soquelitinib in Participants With Moderate to Severe AD

NCT06345404

Phase 1 Completed 82 enrolled Corvus Pharmaceuticals, Inc.
RandomizedSequentialQuadruple-blindTreatment

Summary

Safety, tolerability, and preliminary efficacy of soquelitinib in participants with moderate to severe AD

Timeline

Start
2024-04-16
Primary completion
2026-01-28
Completion
2026-02-24

Drugs

EvaluationDrugModalityDoseRoute
Subject Soquelitinib Small molecule 100 mg Oral
Subject Soquelitinib Small molecule 200 mg Oral

Indications