drugset / Trial / NCT05254405

An Open Label Pilot Study of IV Brexanolone for the Treatment of Post-Traumatic Stress Disorder

NCT05254405 ↗

Phase 4 Terminated 10 enrolled Donald Jeffrey Newport Sage Therapeutics · collab
NaSingle-groupOpen-labelTreatment

Summary

Open-label study of brexanolone infusion for the treatment of posttraumatic stress disorder in 20 adult women with PTSD. Primary Objective: To determine if brexanolone injection infused intravenously for 24 hours at up to 60 μg/kg/h reduces PTSD symptom severity in a group of non-veteran adult female subjects diagnosed with PTSD as assessed by the change from baseline in the PTSD Checklist for DSM-5 (PCL-5) total score and rate of remission at 12-weeks post infusion. Secondary Objectives * To evaluate the safety and tolerability profiles of brexanolone in this PTSD patient population as assessed by the incidence of adverse events (AEs), vital sign measurement, the Stanford Sleepiness Scale (SSS) and the Columbia Suicide Severity Rating Scale (C-SSRS). * To determine the effects of brexanolone in reducing depressive symptoms and improving functional capacity in PTSD patients as assessed by change from baseline in self-assessment Montgomery-Asberg Depression Rating Scale (MADRS-S) total score and Sheehan Disability Scale scores

Timeline

Start
2023-06-01
Primary completion
2025-12-30
Completion
2025-12-30

Outcome

Outcome not reported

Stopped (Business): “Loss of funding.”

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Brexanolone Unknown 90 ug/kg Intravenous