drugset / Trial / NCT06679062
Suvorexant for Treatment of AUD and PTSD
Phase 2
Recruiting
76 enrolled
Pharmacotherapies for Alcohol and Substance Use Disorders Alliance
The University of Texas Health Science Center, Houston · collabUniversity of California, Los Angeles · collab
RandomizedParallel-groupTriple-blindTreatment
Summary
This study is to determine if suvorexant (SUV) will reduce insomnia in 76 men and women veteran and non-veterans between the ages 21-65 with posttraumatic stress disorder (PTSD) symptoms and alcohol use disorder (AUD). All participants will have a 7-day placebo run-in period, followed by a random assignment to receive placebo or suvorexant for an additonal 14 days. Post-randomization, participants will attempt to stop drinking for two weeks and will complete daily virtual diaries and study outcome assessments via in-person clinic visits on days 7 and 14.
Timeline
- Start
- 2025-07-16
- Primary completion
- 2027-03
- Completion
- 2027-03
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Suvorexant | Small molecule | 20 mg | Oral |