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Terminated Phase 3 Interventional

A Study 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 and Long-term Extension Treatment With Aticaprant

ClinicalTrials.gov ID: NCT06514742

Public ClinicalTrials.gov record NCT06514742. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 18, 2026, 2:38 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-blind, Multicenter, 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 and an Open Label Long-term Extension Treatment With Aticaprant

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate how well aticaprant works as compared with placebo when given along with an antidepressant therapy in improving the depressive symptoms in adult participants with major depressive disorder (MDD) with moderate to severe anhedonia (ANH+) who have not responded well to current antidepressant therapy with a selective serotonin reuptake inhibitor/serotonin-norepinephrine reuptake inhibitor (SSRI or SNRI).

Study identification

NCT ID
NCT06514742
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Enrollment
101 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
18 Years to 64 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 26, 2024 (Actual)
Primary completion
Apr 8, 2025 (Actual)
Completion
Apr 24, 2025 (Actual)
Last update posted
Feb 17, 2026

2024 – 2025

United States locations

U.S. sites
39
U.S. states
16
U.S. cities
36
Facility City State ZIP Site status
UAB Huntsville Regional Medical Campus Huntsville Alabama 35801 —
IMA Clinical Research PC Phoenix Arizona 85012 —
Noble Clinical Research Tucson Arizona 85704 —
Advanced Research Center Inc Anaheim California 92805 —
CI Trials Bellflower California 90706 —
Behavioral Research Specialists LLC Glendale California 91206 —
Sun Valley Research Center Imperial California 92251 —
ATP Clinical Research Orange California 92866 —
Lumos Clinical Research Center LLC San Jose California 95124 —
Viking Clinical Research Ltd Temecula California 92591 —
Sunwise Clinical Research Walnut Creek California 94596 —
MCB Clinical Research Centers LLC Colorado Springs Colorado 80910 —
Humanity Clinical Research Corp Aventura Florida 33180 —
Elligo Independent Research Sites Mindful Behavioral Health Boca Raton Florida 33431 —
Gulfcoast Medical Research Center Fort Myers Florida 33912 —
New Life Medical Research Center, Inc. Hialeah Florida 33012 —
LCC Medical Research Institute Inc Miami Florida 33126 —
Floridian Clinical Research LLC Miami Florida 33135 —
Medquest Translational Sciences Miami Lakes Florida 33016 —
Best Choice Medical and Research Service Pembroke Pines Florida 33024 —
K2 Medical Research Tampa Florida 33607 —
Neuroscience Research Institute West Palm Beach Florida 33407 —
Accelerated Clinical Trials LLC Peachtree Corners Georgia 30071 —
Southern Illinois University School of Medicine Springfield Illinois 62702 —
DelRicht Research New Orleans Louisiana 70115 —
CBH Health Gaithersburg Maryland 20877 —
Integrative Clinical Trials LLC Brooklyn New York 11229 —
Fieve Clinical Research Inc New York New York 10017 —
New Hope Clinical Research Charlotte North Carolina 28211 —
Patient Priority Clinical Sites LLC Cincinnati Ohio 45215 —
OSU Department of Psychiatry and Behavioral Health Columbus Ohio 43210 —
Conrad Clinical Research Edmond Oklahoma 73013 —
Suburban Research Associates Media Pennsylvania 19063 —
UTHealth Houston Center for Interventional Psychiatry Houston Texas 77030 —
Brain Health Consultants Houston Texas 77046 —
Red Oak Psychiatry Associates Houston Texas 77090 —
Revival Research Institute LLC McKinney Texas 75071 —
Perceptive Pharma Research Richmond Texas 77407 —
Northwest Clinical Research Center Bellevue Washington 98007 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 45 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06514742, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 17, 2026 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06514742 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →