BENITIONSClinical Trial Intelligence

A Study of Aticaprant Plus an Antidepressant to Prevent Return of Depression Symptoms in Participants With Major Depressive Disorder Who Experience a Loss of Interest and Pleasure

3期 提前终止 NCT06635135

适应症Depressive Disorder, Major, Anhedonia
分期3期
申办方Janssen Research & Development, LLC
状态提前终止
受试者人数47 人
干预(药物)Aticaprant
开始日期2024年9月19日
完成日期2025年4月9日
结果公布日2026年6月8日

摘要

The purpose of this study is to assess how well aticaprant works compared to placebo when given in addition to antidepressant therapy (selective serotonin reuptake inhibitor \[SSRI\] or serotonin-norepinephrine reuptake inhibitor \[SNRI\]) in preventing return of depression symptoms in participants with major depressive disorder who experience a loss of interest and pleasure and who achieve a stable response after treatment with adjunctive aticaprant.

Time From Randomization Into Double Blind (DB) Treatment Maintenance Phase to the First Documentation of Relapse

From date of DB randomization (Day 113) up to first documentation of relapse (up to early termination of study [Day 140]) · days

DB Treatment Maintenance Phase: Aticaprant 10 mgNA days

在 BENITIONS 中查看 查看 ClinicalTrials.gov 原文

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本页整理自 ClinicalTrials.gov 的公开数据,不构成医疗建议,也不构成投资建议。请务必咨询专业医师。