drugset / Trial / NCT03354637

A Study of ATI-50002 Topical Solution for the Treatment of Alopecia Areata

NCT03354637 ↗

Phase 2 Terminated 129 enrolled Aclaris Therapeutics, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

Primary: • To assess safety, tolerability and efficacy of 2 dose strengths of ATI-50002 Topical Solution, compared to vehicle in subjects with alopecia areata (AA) Secondary: • To evaluate key clinical outcome assessments

Timeline

Start
2017-11-29
Primary completion
2019-04-18
Completion
2019-09-10

Outcome

Outcome not reported

Stopped: “The double-blind primary endpoint was not met. Open Label Extension period halted as a result.”

Drugs

EvaluationDrugModalityDoseRoute
Comparator IFIDANCITINIB Small molecule — Topical

Indications