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Clinical Trial 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.


Clinical Trial Description

This is a Phase 2, multicenter, double-blind, placebo-controlled, parallel-group study consisting of a screening period of up to 40 days, a 6 week randomized double-blind treatment period, followed by an up to 2 week safety follow-up period after the last dose of study medication. Patients will be randomized to one of four treatment groups. Patients will participate for a total of up to 10 weeks, including screening, the 6-week treatment period and follow-up. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03797521
Study type Interventional
Source Promentis Pharmaceuticals, Inc.
Contact
Status Completed
Phase Phase 2
Start date December 19, 2018
Completion date December 16, 2019

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