drugset / Trial / NCT03797521
A Study in Patients With Trichotillomania
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | SXC-2023 | Unknown | 50 mg | Oral |
| Subject | SXC-2023 | Unknown | 200 mg | Oral |
| Subject | SXC-2023 | Unknown | 800 mg | Oral |