Trials / Completed
CompletedNCT00130676
A United States Study of Corlux for Psychotic Symptoms in Psychotic Major Depression
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
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 257 (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 56 day study is to learn the safety and effectiveness of Corlux in patients who have been diagnosed with psychotic major depression (PMD).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Mifepristone | daily for 7 days |
| DRUG | matching placebo | daily for 7 days |
Timeline
- Start date
- 2004-09-01
- Primary completion
- 2006-06-01
- Completion
- 2006-06-01
- First posted
- 2005-08-16
- Last updated
- 2012-02-15
Locations
23 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00130676. Inclusion in this directory is not an endorsement.