drugset / Trial / NCT03855865

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

NCT03855865

Phase 3 Withdrawn Naurex, Inc
RandomizedParallel-groupDouble-blindTreatment

Summary

The study will evaluate the efficacy, safety, and tolerability of 450 milligrams (mg) of Rapastinel, compared to 10 mg of Vortixetine and placebo in participants with major depressive disorder (MDD).

Timeline

Start
2019-07-01
Primary completion
2020-12-31
Completion
2020-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Rapastinel Other / unclassified 450 mg Intravenous
Comparator Vortioxetine Unknown 10 mg Oral
Comparator Vortioxetine Unknown 20 mg Oral