Stress Disorders, Post-Traumatic Clinical Trial
Official title:
Phase 2a, Randomized, Double-Blind, Placebo-Controlled Trial Evaluating Efficacy, Safety, and Pharmacokinetics of Orally Administered SNC-102 in Subjects With Combat-Related Posttraumatic Stress Disorder Concomitantly Treated With Prazosin
This is a randomized, double-blind, placebo-controlled study of SNC-102 in adult subjects
with cPTSD, added to pre-existing treatment that includes prazosin with or without other
psychotropic drugs.
Subjects will be treated with SNC-102 tablets or matching placebo on a BID basis for 8
weeks. Subjects will be evaluated for the symptoms of combat-related posttraumatic stress
disorder (cPTSD) as measured by the Clinician Administered PTSD Scale (CAPS-5), compared
with the response to placebo.
n/a
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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