drugset / Trial / NCT00569582

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

NCT00569582

Phase 3 Completed 50 enrolled Corcept Therapeutics
NaSingle-groupOpen-labelTreatment

Summary

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

Timeline

Start
2007-12
Primary completion
2011-01
Completion

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Mifepristone Small molecule Oral

Indications