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CompletedNCT00130676

Mifepristone for psychotic depression

About this title

A United States Study of Corlux for Psychotic Symptoms in Psychotic Major Depression

Read the official source — NCT00130676

Researchers compared Mifepristone and placebo, tracking side effects to assess safety in people with depression.

Medication studyAges 18–75United States
The study in practice

Understand this study

What did researchers investigate?

Researchers compared Mifepristone and placebo, tracking side effects to assess safety in people with depression.

Who was this study for?

This study was for people with depression. Listed age limits: 18 years to 75 years. Other eligibility criteria applied.

Listed locations
Pico Rivera and 22 more locationsSee all locations and recruitment
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Study clarity

Study information

Study start dateSeptember 2004
Recruitment status
Completed
Enrollment listed in the registry
257
Sponsor
Corcept Therapeutics
Sponsor type
Biotech company
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Locations
United States
Age range
From 18 Years to 75 Years
Official registry ID
NCT00130676
Official title
Show the full official title

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

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Recruitment & locations

Completed

Pico Rivera · Riverside · San Diego

20 more locations
  • Jacksonville
  • Pompano Beach
  • Atlanta
  • Oak Brook
  • Greenwood
  • Farmington Hills
  • Las Vegas
  • Clementon
  • Newark
  • Toms River
  • Glen Oaks
  • Lawrence
  • Dayton
  • Lyndhurst
  • Oklahoma City
  • Philadelphia
  • Bellaire
  • Wichita Falls
  • Richmond
  • Bellevue
FAQ

Questions about this study

What did researchers investigate?

Researchers compared Mifepristone and placebo, tracking side effects to assess safety in people with depression.

Who is behind this study?

The study sponsor is Corcept Therapeutics.

Did this study involve medication?

Yes. The study involved medication, including Mifepristone and matching placebo.

Who was this study for?

This study was for people with depression. Listed age limits: 18 years to 75 years. Other eligibility criteria applied.

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