drugset / Trial / NCT02285504

Evaluate SAGE-547 in Female Participants With Severe Postpartum Depression

NCT02285504 ↗

Phase 2 Completed 4 enrolled Supernus Pharmaceuticals, Inc.
NaSingle-groupOpen-labelTreatment

Summary

This is an open-label proof-of-concept study designed to evaluate the safety, tolerability, pharmacokinetics (PK), and efficacy of SAGE-547 Injection in adult female participants diagnosed with severe postpartum depression (PPD).

Timeline

Start
2015-01-07
Primary completion
2015-06-05
Completion
2015-06-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Brexanolone Unknown 86 ug/kg Intravenous

Indications