drugset / Trial / NCT03665038

A Study to Assess the Safety of Brexanolone in the Treatment of Adolescent Female Participants With Postpartum Depression (PPD)

NCT03665038 ↗

Phase 3 Completed 28 enrolled Supernus Pharmaceuticals, Inc.
NaSingle-groupOpen-labelTreatment

Summary

This is a multi-center study evaluating the safety, tolerability, and pharmacokinetics of brexanolone in the treatment of adolescent female participants with postpartum depression (PPD).

Timeline

Start
2018-09-07
Primary completion
2021-01-08
Completion
2021-01-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Brexanolone Unknown 90 ug/kg Intravenous

Indications