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Completed Phase 2 Interventional

A Safety and Effectiveness Study of JNJ-18038683 in Patients With Moderate to Severe Depression

ClinicalTrials.gov ID: NCT00566202

Public ClinicalTrials.gov record NCT00566202. 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 21, 2026, 8:16 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 Phase IIa Multicenter, Randomized, Double-blind, Double-dummy, and Placebo- and Active Controlled Study to Investigate the Safety and Efficacy of JNJ-18038683 Administered to Subjects With Major Depressive Disorder

Brief summary

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

The purpose of this study is to evaluate the safety and effectiveness of JNJ-18038683 compared to escitalopram and placebo in patients with moderate to severe depression.

Study identification

NCT ID
NCT00566202
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
67 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 60 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
Dec 2007 (Type not available)
Primary completion
Dec 2008 (Actual)
Completion
Dec 2008 (Actual)
Last update posted
Aug 6, 2014

2007 – 2008

United States locations

U.S. sites
26
U.S. states
17
U.S. cities
26
Facility City State ZIP Site status
Not listed Little Rock Arkansas — —
Not listed Beverly Hills California — —
Not listed Glendale California — —
Not listed San Diego California — —
Not listed Bradenton Florida — —
Not listed Maitland Florida — —
Not listed Orlando Florida — —
Not listed Atlanta Georgia — —
Not listed Eagle Idaho — —
Not listed Chicago Illinois — —
Not listed Prairie Village Kansas — —
Not listed Topeka Kansas — —
Not listed Baton Rouge Louisiana — —
Not listed Shreveport Louisiana — —
Not listed Nutley New Jersey — —
Not listed Brooklyn New York — —
Not listed Cedarhurst New York — —
Not listed Fresh Meadows New York — —
Not listed Cincinnati Ohio — —
Not listed Oklahoma City Oklahoma — —
Not listed Portland Oregon — —
Not listed Norristown Pennsylvania — —
Not listed Memphis Tennessee — —
Not listed Austin Texas — —
Not listed Irving Texas — —
Not listed Richmond Virginia — —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00566202, 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 Aug 6, 2014 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00566202 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →