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ACTIVE NOT RECRUITING
NCT05223829
PHASE1

Utility of Brexanolone to Target Stress-induced Alcohol Use Among Men and Women With Posttraumatic Stress Disorder

Sponsor: Yale University

View on ClinicalTrials.gov

Summary

For this protocol, the investigators plan to collect pilot data to: 1. establish the feasibility and safety of administering brexanolone to individuals with concurrent Posttraumatic Stress Disorder (PTSD) and Alcohol Use Disorder (AUD).

Key Details

Gender

All

Age Range

21 Years - 55 Years

Study Type

INTERVENTIONAL

Enrollment

25

Start Date

2023-08-01

Completion Date

2025-12-31

Last Updated

2025-10-14

Healthy Volunteers

No

Interventions

DRUG

Brexanolone

Brexanolone will be administered as a continuous IV infusion over 20 hours under medical observation

Locations (1)

Yale School of Medicine

New Haven, Connecticut, United States