drugset / Trial / NCT03797521

A Study in Patients With Trichotillomania

NCT03797521 ↗

Phase 2 Completed 128 enrolled Promentis Pharmaceuticals, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to explore the safety, tolerability and activity of SXC-2023 when dosed for 6 weeks versus placebo in adult patients with moderate to severe Trichotillomania.

Timeline

Start
2018-12-19
Primary completion
2019-12-02
Completion
2019-12-16

Drugs

EvaluationDrugModalityDoseRoute
Subject SXC-2023 Unknown 50 mg Oral
Subject SXC-2023 Unknown 200 mg Oral
Subject SXC-2023 Unknown 800 mg Oral

Indications