drugset / Trial / NCT05401565

Study To Evaluate The Efficacy And Safety Of Balovaptan In Adults With Post-Traumatic Stress Disorder (PTSD)

NCT05401565

Phase 2 Completed 29 enrolled Hoffmann-La Roche
RandomizedParallel-groupDouble-blindTreatment

Summary

This study will evaluate the efficacy and safety of 10 mg of oral administration balovaptan once a day (QD) compared with matching placebo in adults with PTSD.

Timeline

Start
2022-08-02
Primary completion
2023-10-05
Completion
2023-10-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Balovaptan Small molecule 10 mg Oral