CompletedPhase 3NCT00936741
An Extension Study of CORLUX in the Treatment of Endogenous Cushing's Syndrome
Studying OBSOLETE: Cushing syndrome
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Corcept Therapeutics
- Principal Investigator
- Coleman Gross, MDCorcept Therapeutics
- Intervention
- mifepristone(drug)
- Enrollment
- 30 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2009 – 2012
Study locations (15)
- University of Alabama at Birmingham School of Medicine, Birmingham, Alabama, United States
- AMCR Institute Inc., Escondido, California, United States
- Stanford University Medical Center, Stanford, California, United States
- The Center for Diabetes and Endocrine Care, Hollywood, Florida, United States
- Northwestern University Feinberg Medical; Division of Endocrinology, Metabolism & Molecular Medicine, Chicago, Illinois, United States
- Sinai Hospital of Baltimore, Baltimore, Maryland, United States
- Massachusetts General Hospital, Boston, Massachusetts, United States
- University of Michigan Medical Center, Ann Arbor, Michigan, United States
- University of Mississippi Medical Center, Jackson, Mississippi, United States
- University of New Mexico, Albuquerque, New Mexico, United States
- Cleveland Clinic Foundation; Dept of Endocrinology, Diabetes & Metabolism, Cleveland, Ohio, United States
- Oklahoma Diabetes Center, Oklahoma City, Oklahoma, United States
- Oregon Health Sciences University, Portland, Oregon, United States
- University of Texas Southwestern Medical Center, Dallas, Texas, United States
- Endocrinology Center at Community Medical Commons, Menomonee Falls, Wisconsin, United States
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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