drugset / Trial / NCT02978326

A Study to Evaluate SAGE-217 in Participants With Severe Postpartum Depression

NCT02978326

Phase 3 Completed 276 enrolled Biogen
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary purpose of this study was to determine if treatment with SAGE-217 reduces depressive symptoms in participants with severe postpartum depression (PPD) compared to placebo as assessed by the change from baseline in the 17-item Hamilton Rating Scale for Depression (HAM-D) total score at Day 15 and to evaluate the safety and tolerability of SAGE-217 compared to placebo as assessed by the incidence of adverse events, vital sign measurements, clinical laboratory evaluations, electrocardiogram (ECG) parameters, and the Columbia Suicide Severity Rating Scale (C-SSRS).

Timeline

Start
2017-01-04
Primary completion
2018-11-15
Completion
2018-12-11

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Zuranolone Small molecule 15 mg Oral
Subject Zuranolone Small molecule 20 mg Oral
Subject Zuranolone Small molecule 30 mg Oral

Indications