drugset / Trial / NCT03352453

A Study of Rapastinel for Rapid Treatment of Depression and Suicidality in Major Depressive Disorder

NCT03352453

Phase 2 Terminated 138 enrolled Naurex, Inc
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The study will evaluate the efficacy, safety, and tolerability of 450 milligrams (mg) of Rapastinel, compared to placebo in adult patients with major depressive disorder (MDD) who are at imminent risk of suicide.

Timeline

Start
2017-12-15
Primary completion
2019-06-21
Completion
2019-06-21

Drugs

EvaluationDrugModalityDoseRoute
Subject Rapastinel Other / unclassified 450 mg Intravenous