drugset / Trial / NCT02418585

A Study to Evaluate the Efficacy, Safety, and Tolerability of Flexible Doses of Intranasal Esketamine Plus an Oral Antidepressant in Adult Participants With Treatment-resistant Depression

NCT02418585

Phase 3 Completed 236 enrolled Janssen Research & Development, LLC
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to compare the efficacy and safety of switching treatment-resistant depression (TRD) subjects from a prior antidepressant treatment (to which they have not responded) to either intranasal esketamine plus a new oral antidepressant or switching to a new oral antidepressant plus intranasal placebo.

Timeline

Start
2015-08-07
Primary completion
2017-06-01
Completion
2017-11-06

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Esketamine Other / unclassified 56 mg Intranasal
Subject Esketamine Other / unclassified 84 mg Intranasal
Background Duloxetine Small molecule 60 mg Oral
Background Escitalopram Small molecule 10 mg Oral
Background Escitalopram Small molecule 20 mg Oral
Background Sertraline Small molecule 50 mg Oral
Background Sertraline Small molecule 150 mg Oral
Background Venlafaxine Small molecule 150 mg Oral
Background Venlafaxine Small molecule 225 mg Oral

Indications

No indication recorded.