Safety and Efficacy of CORLUX™ (Mifepristone) for depression
This study is completed in the United States. It is testing Safety and Efficacy of CORLUX™ (Mifepristone) for depression.
Depression, SchizophreniaDrugFrom 18 Years to 75 Years
The public registry lists this study as not currently recruiting. This page remains available for information. Check the official record for the latest status and explore other recruiting studies.
Then choose your country and confirm availability with each study site.
In plain English
Key information made simple
What is this study testing?
This study is testing whether Corlux may be useful for adults experiencing depression.
What would participation involve?
Participants may receive Corlux, attend study visits with the research team. The protocol may also involve randomization, placebo, or a comparison group. The registry lists locations in the United States.
Who is it mainly for?
This study appears to be mainly for adults with depression.
What should you check before joining?
Ask about the dose, safety monitoring, and possible side effects, whether there is placebo, randomization, or a comparison group, how many visits or travel steps are needed, the exact eligibility criteria.
Your next step
Check the study details
Check the official source, then confirm these points with the research team.
Where are visits, can any be remote, and how much time is needed?
Costs and support
What costs, reimbursement or compensation apply?
Before joining
Questions to ask before joining
What are the exact eligibility criteria, and what could exclude someone?
How many visits, assessments, or follow-ups are expected, and over what period?
What risks, side effects, practical burdens, or alternatives should be understood first?
Who should be contacted to confirm locations, timing, compensation, and next steps?
Study clarity
Things to check before joining
Study start dateSeptember 2004
Recruitment status
Completed
Enrollment listed in the registry
257
Sponsor
Corcept Therapeutics
Sponsor type
Biotech company
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Locations
United States
Age range
From 18 Years to 75 Years
Official registry ID
NCT00130676
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
Check recruitment and locations
Recruitment checked against the registry by HopeStage on . Registry information can change. Always confirm availability with the research team.
The overall study status can differ from each site's status. Open a country to see its locations and their registry status.
United States · 23 sites
CNRI-LA
Pico Rivera, California
Site status: Not listed — confirm with the team
Behavioral Health 2000, LLC
Riverside, California
Site status: Not listed — confirm with the team
Cnri, Llc
San Diego, California
Site status: Not listed — confirm with the team
University of Florida Clinical Trials
Jacksonville, Florida
Site status: Not listed — confirm with the team
Quantum Laboratories/Memory Disorder Center
Pompano Beach, Florida
Site status: Not listed — confirm with the team
Atlanta Center for Medical Research
Atlanta, Georgia
Site status: Not listed — confirm with the team
American Medical Research, Inc.
Oak Brook, Illinois
Site status: Not listed — confirm with the team
Valle Vista Health System
Greenwood, Indiana
Site status: Not listed — confirm with the team
Psychopharmacology Research
Farmington Hills, Michigan
Site status: Not listed — confirm with the team
Robert Horne, MD
Las Vegas, Nevada
Site status: Not listed — confirm with the team
CNS Research Institute
Clementon, New Jersey
Site status: Not listed — confirm with the team
NMDNJ
Newark, New Jersey
Site status: Not listed — confirm with the team
Bio Behavioral Health
Toms River, New Jersey
Site status: Not listed — confirm with the team
Zucker Hillside Hospital
Glen Oaks, New York
Site status: Not listed — confirm with the team
Neurobehavioral Research Company
Lawrence, New York
Site status: Not listed — confirm with the team
Midwest Clinical Research Center
Dayton, Ohio
Site status: Not listed — confirm with the team
Rakesh Ranjan, MD and Associates, Inc
Lyndhurst, Ohio
Site status: Not listed — confirm with the team
IPS Research Company
Oklahoma City, Oklahoma
Site status: Not listed — confirm with the team
CNS Research Institute
Philadelphia, Pennsylvania
Site status: Not listed — confirm with the team
Claghorn-Lesem Research Clinic
Bellaire, Texas
Site status: Not listed — confirm with the team
Grayline Clinical Drug Trials
Wichita Falls, Texas
Site status: Not listed — confirm with the team
International Clinical Research Associates
Richmond, Virginia
Site status: Not listed — confirm with the team
Northwest Clinical Research Center
Bellevue, Washington
Site status: Not listed — confirm with the team
Ask HopeStage to help me review this study
This record does not confirm open recruitment. We can help you understand it and explore other studies.
Study ID: NCT00130676. We help you review the study, but cannot decide medical eligibility.
In practice
For you
Participation may contribute to research. Personal benefit is not guaranteed.
Ask the research team to explain the activities, time commitment, and follow-up involved.
Study sites are listed. Confirm the relevant site and any travel before making plans.
Important
Not medical advice
Information from public sources.
Are you the study sponsor? Contact us to update this page: hi@hopestage.com
FAQ
Questions about this study
What is this study trying to understand?
This study is exploring medication or study treatment for people with depression. Participants may complete study visits, assessments, or follow-up activities defined by the research team. Direct benefit is not guaranteed. The detailed objective is not always clearly listed in the public registry; the study team can confirm.
Does this study involve a medication?
This appears to be a medication / drug study involving Mifepristone, matching placebo. Phase 3 studies are usually larger and aim to confirm effectiveness and safety in a broader group.
Who might this study be for?
This study may concern people with depression; age range: From 18 Years to 75 Years. The criteria appear fairly specific, but you should not assume you are eligible. The study team must confirm diagnosis, age, exclusions, available locations, and next steps.
What would I likely need to do?
You may need to take a study treatment and have regular medical follow-up. The listed study locations suggest that at least part of participation may involve a physical site. Ask whether some steps can be done remotely.
What side effects, interactions, or treatment changes should I check?
If the study involves a medication, ask whether it is already approved, experimental, or being tested for a new use. Check possible side effects, interactions with current treatment, dose changes, monitoring, and what happens if you feel worse. For any mental health study, also ask who to contact if you feel worse, whether participation may affect current treatment, whether you can stop, and who confirms eligibility.
Will I need to travel or attend in-person visits?
The listed study locations suggest that at least part of participation may involve a physical site. Ask which sites are open, how many visits are expected, whether any steps can be done remotely, and whether travel costs or compensation are listed.
Who is behind this study?
This study is sponsored by Corcept Therapeutics, which appears to be a biotech company. If available, it can be useful to check the sponsor website, collaborators, investigator affiliation, and the official registry before deciding. HopeStage does not judge the quality of a sponsor or researcher, but helps you identify what to verify.
Can I still join this study?
The public registry lists this study as not currently recruiting. This page remains available for information. Check the official record for the latest status and explore other recruiting studies.
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