A Study of JNJ-61393215 in the Treatment of Depression

  • participants needed
  • sponsor
    Janssen Research & Development, LLC
Updated on 6 December 2021


The purpose of this study is to evaluate the efficacy of JNJ-61393215 as adjunctive treatment compared to adjunctive placebo, as assessed by the change from baseline to week 6 on a 17-item Hamilton Depression Rating Scale (HDRS-17) in participants with major depressive disorder (MDD) with anxious distress with a score greater than or equal to (>=) 2 on item 26 or 27 of the Inventory of Depressive Symptomatology, Clinician Rating -30 (IDS-C30), who have a suboptimal response to current treatment with a standard antidepressant.

Condition Major Depressive Disorder With Anxious Distress
Treatment Placebo, JNJ-61393215
Clinical Study IdentifierNCT04080752
SponsorJanssen Research & Development, LLC
Last Modified on6 December 2021

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