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Completed Phase 3 Interventional

A United States Study of Corlux for Psychotic Symptoms in Psychotic Major Depression

ClinicalTrials.gov ID: NCT00130676

Public ClinicalTrials.gov record NCT00130676. 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 Jul 22, 2026, 8:57 AM 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, Placebo-Controlled Study of Safety and Efficacy of CORLUX™ (Mifepristone) in the Treatment of Psychotic Symptoms in Patients With Major Depressive Disorder With Psychotic Features

Study identification

NCT ID
NCT00130676
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Corcept Therapeutics
Industry
Enrollment
257 participants

Conditions and interventions

Interventions

  • Mifepristone Drug
  • matching placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 75 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
Aug 31, 2004
Primary completion
May 31, 2006
Completion
May 31, 2006
Last update posted
Feb 14, 2012

2004 – 2006

United States locations

U.S. sites
23
U.S. states
15
U.S. cities
23
Facility City State ZIP Site status
CNRI-LA Pico Rivera California 90660
Behavioral Health 2000, LLC Riverside California 92506
Cnri, Llc San Diego California 92126
University of Florida Clinical Trials Jacksonville Florida 32257
Quantum Laboratories/Memory Disorder Center Pompano Beach Florida 33064
Atlanta Center for Medical Research Atlanta Georgia 30308
American Medical Research, Inc. Oak Brook Illinois 60523
Valle Vista Health System Greenwood Indiana 46143
Psychopharmacology Research Farmington Hills Michigan 48334
Robert Horne, MD Las Vegas Nevada 89102
CNS Research Institute Clementon New Jersey 08021
NMDNJ Newark New Jersey 07101
Bio Behavioral Health Toms River New Jersey 08755
Zucker Hillside Hospital Glen Oaks New York 11004
Neurobehavioral Research Company Lawrence New York 11559
Midwest Clinical Research Center Dayton Ohio 45408
Rakesh Ranjan, MD and Associates, Inc Lyndhurst Ohio 44124
IPS Research Company Oklahoma City Oklahoma 73101
CNS Research Institute Philadelphia Pennsylvania 19149
Claghorn-Lesem Research Clinic Bellaire Texas 77401
Grayline Clinical Drug Trials Wichita Falls Texas 76309
International Clinical Research Associates Richmond Virginia 23229
Northwest Clinical Research Center Bellevue Washington 98004

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 NCT00130676, 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 14, 2012 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00130676 live on ClinicalTrials.gov.

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