Status:
TERMINATED
A Study of Mifepristone vs. Placebo in the Treatment of Patients With Major Depression With Psychotic Features
Lead Sponsor:
Corcept Therapeutics
Conditions:
Psychotic Depression
Severe Major Depression With Psychotic Features
Eligibility:
All Genders
22+ years
Phase:
PHASE3
Brief Summary
Approximately 450 patients will be randomized to receive mifepristone or placebo for 7 days followed by antidepressant. The purpose is to compare the efficacy of mifepristone followed by antidepressan...
Detailed Description
Up to 450 patients with psychotic depression will be randomly assigned to receive either mifepristone or matching placebo. Patients will be assessed by the investigator or site staff during screening ...
Eligibility Criteria
Inclusion
- Have provided written consent to participate in the study prior to any study procedures and understand that they are free to withdraw from the study at any time. Patients must be able to read and understand the consent form, complete study-related procedures, and communicate with the study staff
- Have a DSM-IV TR diagnosis of Major Depressive Disorder with Psychotic Features (DSM-IV 296.24 or 296.34), and are clinically symptomatic with their illness
- Have pre-specified minimum scores on standardized psychiatric rating scales at baseline
- Have not been taking excluded medication for at least 7 days prior to randomization
- Have a negative pregnancy test
- If not postmenopausal for ≥ 2 years or surgically sterile (6 months post-surgery), must consent (patient or partner) to utilize two medically acceptable methods of contraception, one of which is a barrier method, throughout the entire study period and for 3 months after the study is completed
Exclusion
- Have any primary psychiatric diagnosis other than psychotic depression.
- Have a major medical problem, which in the opinion of the investigator would place the patient at undue risk.
- Have undergone electroconvulsive therapy within 3 months prior to randomization
- Have had a hospitalization due to a suicide attempt within 45 days prior to randomization
- Are female and of childbearing age, and are unable or unwilling to use two medically acceptable methods of contraception during the study and for three months after study completion, one of which must be a barrier method
- Are female and are pregnant or lactating
- Are currently taking excluded medications
- Have used drugs of abuse within 30 days prior to screen, as per patient report and urine drug screen
- Have a history of active drug or alcohol abuse within 3 months or dependence within 6 months prior to screening
- Are in the opinion of the investigator at immediate risk of suicide, or at risk of harming others
- Have received investigational therapy (drug, vaccine, biological agent or device) within 6 months prior to randomization
- Have previously participated in a clinical trial of mifepristone
- Have a history of an allergic reaction to mifepristone
- Are in the investigator's opinion not appropriate for participation in the study or may not be capable of following the study schedule for any reason
- Are patients who are employees of the study unit or their family members, students who are working in the study unit, or family members of the investigator or Corcept Therapeutics
Key Trial Info
Start Date :
March 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 1 2014
Estimated Enrollment :
292 Patients enrolled
Trial Details
Trial ID
NCT00637494
Start Date
March 1 2008
End Date
June 1 2014
Last Update
June 5 2017
Active Locations (42)
Enter a location and click search to find clinical trials sorted by distance.
1
K&S Professional Research Services, LLC
Little Rock, Arkansas, United States, 72201
2
Woodland International Research Group, Inc.
Little Rock, Arkansas, United States, 72211
3
South Coast Clinical Trials, Inc
Anaheim, California, United States, 92804
4
Diligent Clinical Trials
Downey, California, United States, 90241