Clinical Trials Directory

Trials / Completed

CompletedNCT00128505

An International Extension Study of Corlux for Recurrent Psychotic Symptoms in Psychotic Major Depression

An International, Open-Label Extension Study of the Safety and Tolerability of CORLUX™ (Mifepristone) for Recurrent Psychotic Symptoms in Patients With Major Depressive Disorder With Psychotic Features

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
104 (actual)
Sponsor
Corcept Therapeutics · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Corlux (mifepristone) is a new medication that modulates the body's use of a hormone called cortisol. Under normal conditions, cortisol and other hormones are created by the body in response to physical and emotional stress, triggering a healthy stress response. People who suffer from psychotic major depression may have unusually high levels of cortisol circulating within them or abnormal patterns of cortisol levels, overloading the stress response mechanism and causing symptoms of psychosis such as delusional thoughts or hallucinations. If Corlux can keep the body's cortisol receptors from being overloaded, the stress response system may return to normal function, which may result in improvement of symptoms. The purpose of this study is to allow patients who have already participated in an earlier 8 week study of Corlux versus placebo (an inactive pill) to receive additional courses of treatment with Corlux periodically if a psychotic episode should reappear during a period of one year.

Conditions

Interventions

TypeNameDescription
DRUGMifepristone

Timeline

Start date
2005-08-01
Primary completion
2006-11-01
Completion
2006-11-01
First posted
2005-08-10
Last updated
2012-02-15

Locations

19 sites across 4 countries: Bulgaria, Croatia, Romania, Serbia

Source: ClinicalTrials.gov record NCT00128505. Inclusion in this directory is not an endorsement.