Status:

COMPLETED

Safety & Efficacy Study of Quetiapine Fumarate (SEROQUEL®) vs. Placebo in Major Depressive Disorder

Lead Sponsor:

AstraZeneca

Conditions:

Major Depressive Disorder

Eligibility:

All Genders

18-65 years

Phase:

PHASE3

Brief Summary

This study is to evaluate that (SEROQUEL®) quetiapine sustained-release is efficacious and safe in the treatment of patients with MDD.

Eligibility Criteria

Inclusion

  • Patient has a documented clinical diagnosis of Major Depressive Disorder.
  • Be able to understand and comply with the requirements of the study.
  • Able to understand and provide written informed consent

Exclusion

  • Patients (female) must not be pregnant or lactating
  • Current or past diagnosis of stroke or transient ischemic attack (TIA).

Key Trial Info

Start Date :

April 1 2006

Trial Type :

INTERVENTIONAL

End Date :

May 1 2007

Estimated Enrollment :

600 Patients enrolled

Trial Details

Trial ID

NCT00320268

Start Date

April 1 2006

End Date

May 1 2007

Last Update

March 25 2009

Active Locations (37)

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Page 1 of 10 (37 locations)

1

Research Site

Little Rock, Arkansas, United States

2

Research Site

Newport Beach, California, United States

3

Research Site

Northridge, California, United States

4

Research Site

Oceanside, California, United States