drugset / Trial / NCT03614156

Study of Monotherapy Rapastinel in the Prevention of Relapse in Patients With Major Depressive Disorder (MDD)

NCT03614156

Phase 3 Terminated 363 enrolled Naurex, Inc
RandomizedParallel-groupDouble-blindTreatment

Summary

The study will evaluate the efficacy, safety, and tolerability of 450 milligrams (mg) or 225 mg of Rapastinel compared to placebo in the prevention of relapse in participants with major depressive disorder (MDD).

Timeline

Start
2018-08-02
Primary completion
2019-07-11
Completion
2019-07-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Rapastinel Other / unclassified 225 mg Intravenous
Subject Rapastinel Other / unclassified 450 mg Intravenous