drugset / Trial / NCT03675776

Study of Rapastinel as Monotherapy in Patients With Major Depressive Disorder (MDD)

NCT03675776

Phase 3 Terminated 50 enrolled Naurex, Inc
RandomizedParallel-groupDouble-blindTreatment

Summary

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

Timeline

Start
2018-10-30
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