drugset / Trial / NCT02932943

A Study of Rapastinel as Adjunctive Therapy in Major Depressive Disorder (RAP-MD-01)

NCT02932943 ↗

Phase 3 Completed 465 enrolled Naurex, Inc
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study will evaluate the efficacy, safety, and tolerability of rapastinel 450 mg compared to placebo adjunctive to antidepressant therapy (ADT) in patients with major depressive disorder (MDD) who have a partial response to ADT.

Timeline

Start
2016-10-15
Primary completion
2018-09-21
Completion
2018-11-08

Outcome

Missed primary endpoint

registry analysis (superiority test); Placebo vs Rapastinel 450 mg; p = 0.6482; Least Squares Mean Difference 0.3 (95% CI -1.07 to 1.72); NCT02932943 ↗

release “In three acute studies (RAP-MD-01,-02,-03), the rapastinel treatment arms did not differentiate from placebo on the primary and key secondary endpoints.” abbvie.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Rapastinel Other / unclassified 450 mg Intravenous