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A Study of Aticaprant in Adult and Elderly Participants With Major Depressive Disorder (MDD)
NCT05518149 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to assess the long-term safety and tolerability of aticaprant administered as adjunctive therapy to a current antidepressant (selective serotonin reuptake inhibitor \[SSRI\] or serotonin and norepinephrine reuptake inhibitor \[SNRI\]) in all participants with major depressive disorder (MDD).
Conditions Studied
Interventions
- DRUG Aticaprant
Study Locations (20)
California
- Advanced Research Center Inc — Anaheim
- Proscience Research Group — Culver City
- Behavioral Research Specialists LLC — Glendale
- Sunwise Clinical Research — Lafayette
- Asclepes Research — Long Beach
- Excell Research Inc — Oceanside
- Pacific Neuropsychiatric Specialists — Orange
- Prospective Research Innovations Inc — Rancho Cucamonga
- University of California San Diego Medical Center — San Diego
- Syrentis Clinical Research — Santa Ana
- CMB Clinical Trials — Santee
- California Neuroscience Research — Sherman Oaks
- Viking Clinical Research Ltd — Temecula
- Pacific Clinical Research Medical Group — Upland
- Next Level Clinical Trials, LLC — West Covina
Arizona
- SW Biomedical Research LLC — Tucson
- University of Arizona — Tucson
Alabama
- University of Alabama at Birmingham - The Kirklin Clinic — Birmingham
Colorado
- MCB Clinical Research Centers LLC — Colorado Springs
Connecticut
- University of Connecticut Health Center — Farmington
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 840 participants |
| Start Date | 2022-09-22 |
| Est. Completion | 2025-04-25 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05518149
The ClinicalTrials.gov registry entry for NCT05518149 describes a study currently listed as active not recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 840 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Janssen Research & Development, which has 442 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Depressive Disorder, Major appearing as the primary indexed condition, and to 1 intervention — of which Aticaprant is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT05518149 reports 20 study locations spanning 5 distinct geographic areas — top geographies include California, Arizona, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT05518149 about?
NCT05518149 is a clinical study titled "A Study of Aticaprant in Adult and Elderly Participants With Major Depressive Disorder (MDD)". The purpose of this study is to assess the long-term safety and tolerability of aticaprant administered as adjunctive therapy to a current antidepressant (selective serotonin reuptake inhibitor \[SSRI\] or serotonin and norepinephrine reuptake inhibitor \[SNRI\]) in all participants with major depre...
What is the current status of trial NCT05518149?
This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 840 participants. The study started on 2022-09-22. Estimated completion is 2025-04-25.
What conditions does trial NCT05518149 study?
This clinical trial studies the following conditions: Depressive Disorder, Major. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT05518149?
The interventions under investigation include: Aticaprant (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT05518149?
This trial is sponsored by Janssen Research & Development, which has 442 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT05518149 being conducted?
This trial has 20 study locations across Alabama, Arizona, California, Colorado, Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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