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Completed Phase 3 Interventional Results available

A Study of the Efficacy and Safety of CORLUX in the Treatment of Endogenous Cushing's Syndrome

ClinicalTrials.gov ID: NCT00569582

Public ClinicalTrials.gov record NCT00569582. 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, 12:28 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

An Open-label Study of the Efficacy and Safety of CORLUX (Mifepristone) in the Treatment of the Signs and Symptoms of Endogenous Cushing's Syndrome

Brief summary

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

Patients will receive Corlux (mifepristone) daily for up to 24 weeks. Assessments of the signs and symptoms of Cushing's syndrome will be obtained.

Study identification

NCT ID
NCT00569582
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Corcept Therapeutics
Industry
Enrollment
50 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Jan 2011 (Actual)
Completion
Not listed
Last update posted
Aug 22, 2013

Started 2007

United States locations

U.S. sites
17
U.S. states
14
U.S. cities
16
Facility City State ZIP Site status
University of Alabama at Birmingham School of Medicine Birmingham Alabama 35294 —
AMCR Institute Inc. Escondido California 92026 —
Stanford University Medical Center Stanford California 94305-5826 —
The Center for Diabetes and Endocrine Care Hollywood Florida 33021 —
Northwestern University Feinberg Medical; Division of Endocrinology, Metabolism & Molecular Medicine Chicago Illinois 60611 —
The University of Chicago Chicago Illinois 60637 —
Sinai Hospital of Baltimore Baltimore Maryland 21215 —
Massachusetts General Hospital Boston Massachusetts 02114 —
University of Michigan Medical Center Ann Arbor Michigan 48109 —
University of Mississippi Medical Center Jackson Mississippi 39216 —
University of New Mexico HSC Albuquerque New Mexico 87131 —
Cleveland Clinic Foundation; Dept of Endocrinology, Diabetes & Metabolism Cleveland Ohio 44195 —
Oklahoma University Health Science Center Oklahoma City Oklahoma 73104 —
Oregon Health Sciences University Portland Oregon 97239 —
University of Texas Southwestern Medical Center Dallas Texas 75390 —
Diabetes and Glandular Disease Clinic San Antonio Texas 78229 —
Endocrinology Center at North Hills, Froedtert and Medical College of Wisconsin Menomonee Falls Wisconsin 53051 —

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 NCT00569582, 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 22, 2013 · 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 NCT00569582 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →