NCT05550532

A Study of Aticaprant 10 Milligrams (mg) as Adjunctive Therapy in Adult Participants With MDD With Moderate-to-severe Anhedonia and Inadequate Response to Current Antidepressant Therapy

A Randomized, Double-blind, Multicenter, Parallel-group, Placebo-controlled Study to Evaluate the Efficacy, Safety, and Tolerability of Aticaprant 10 mg as Adjunctive Therapy in Adult Participants With Major Depressive Disorder (MDD) With Moderate-to-severe Anhedonia and Inadequate Response to Current Antidepressant Therapy

• Status: Completed
• Phase: Phase 3
• Study type: Interventional
• Enrollment: 444 (actual)
• Sponsor: Janssen Research & Development, LLC · Industry
• Sex: All
• Age: 18 Years – 74 Years
• Healthy volunteers: Not accepted

Summary

The purpose of this study is to evaluate the efficacy of aticaprant compared with placebo as adjunctive therapy to an antidepressant in improving depressive symptoms in adult participants with major depressive disorder (MDD) with moderate to severe anhedonia (ANH+) who have had an inadequate response to current antidepressant therapy with a selective serotonin reuptake inhibitor (SSRI) or serotonin-norepinephrine reuptake inhibitor (SNRI).

Detailed description

Depression is a common and serious psychiatric disorder which is a leading cause of disability worldwide and is associated with elevated mortality and suicide risk. Aticaprant (JNJ-67953964) is a once daily, highly selective kappa opioid receptor (KOR) antagonist, with demonstrated selectivity over mu opioid receptor (MOR) and delta opioid receptor (DOR) being developed for adjunctive treatment of MDD with ANH+. The total duration of the study will be up to 87 days. Safety evaluation including adverse events, physical examinations, urine drug test, alcohol breath tests and clinical laboratory tests will be assessed at specific time points during this study.

Conditions

• Depressive Disorder, Major
• Anhedonia

Interventions

Type	Name	Description
DRUG	Aticaprant	Aticaprant tablet will be administered orally.
OTHER	Placebo	Placebo tablet will be administered orally.

Timeline

• Start date: 2022-12-06
• Primary completion: 2024-11-08
• Completion: 2024-11-13
• First posted: 2022-09-22
• Last updated: 2026-02-13
• Results posted: 2026-01-02

Locations

131 sites across 14 countries: United States, Argentina, Brazil, Bulgaria, Canada, China, Czechia, France, Poland, Slovakia, South Africa, South Korea, Taiwan, United Kingdom

Regulatory

• FDA-regulated drug study