A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety and Efficacy of 50 mg NYX-783 Once Daily Compared to Placebo in Participants with Post-Traumatic Stress Disorder (PTSD)
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
121
CAPS-5 (Clinician-Administered PTSD Scale for the Diagnostic and Statistical Manual of' Mental Disorders, 5th edition)
Change from Baseline in CAPS-5
Time frame: study endpoint, up to 10 weeks
CGI-S (Clinician Global Impression - Severity)
Change from Baseline in CGI-S
Time frame: study endpoint, up to 10 weeks
PGI-S (Patient Global Impression - Severity)
Change from Baseline in PGI-S
Time frame: study endpoint, up to 10 weeks
SDS (Sheehan Disability Scale)
Change from Baseline in SDS
Time frame: study endpoint, up to 10 weeks
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Aptinyx Clinical Site
Tuscaloosa, Alabama, United States
Aptinyx Clinical Site
Phoenix, Arizona, United States
Aptinyx Clinical Site
Bentonville, Arkansas, United States
Aptinyx Clinical Site
Bellflower, California, United States
Aptinyx Clinical Site
Glendale, California, United States
Aptinyx Clinical Site
La Jolla, California, United States
Aptinyx Clinical Site
Oceanside, California, United States
Aptinyx Clinical Site
Riverside, California, United States
Aptinyx Clinical Site
Santa Ana, California, United States
Aptinyx Clinical Site
Temecula, California, United States
...and 27 more locations