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Safety and Efficacy of NYX-783 in Subjects With Post-Traumatic Stress Disorder

Post-Traumatic Stress Disorder Clinical Trial

Official title:
A Study to Evaluate the Safety and Efficacy of NYX-783 in Subjects With Post-Traumatic Stress Disorder

Clinical Trial Summary

To evaluate the safety, tolerability, and response profile of NYX-783 in a Post-Traumatic Stress Disorder population.

Clinical Trial Description

The study will be a 10 to 12-week study, including a 1 to 3-week screening Period, followed by a double-blind, randomized, placebo-controlled, parallel-group Treatment Period, and a 1-week follow-up Period. Subjects eligible for the study will be randomized to receive either NYX-783 (4-weeks) or placebo (4 or 8-weeks). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04044664
Study type Interventional
Source Aptinyx
Contact
Status Completed
Phase Phase 2
Start date January 25, 2019
Completion date August 5, 2020
View Details
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