drugset / Trial / NCT03560518

Study of Rapastinel as Monotherapy in Patients With MDD

NCT03560518

Phase 3 Terminated 439 enrolled Naurex, Inc
RandomizedParallel-groupDouble-blindTreatment

Summary

The study will evaluate the efficacy, safety, and tolerability of 450 milligrams (mg) and 900 milligrams (mg) of Rapastinel, compared to placebo in participants with major depressive disorder (MDD).

Timeline

Start
2018-06-15
Primary completion
2019-07-08
Completion
2019-07-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Rapastinel Other / unclassified 450 mg Intravenous
Subject Rapastinel Other / unclassified 900 mg Intravenous