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Completed Phase 3 Interventional

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

ClinicalTrials.gov ID: NCT00320268

Public ClinicalTrials.gov record NCT00320268. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 27, 2026, 2:50 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Double-Blind, Randomized, Parallel-Group, Placebo-Controlled Phase III Study of the Efficacy and Safety of Quetiapine Fumarate Sustained-Release (SEROQUEL®) as Monotherapy in the Treatment of Patients With MDD

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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

Study identification

NCT ID
NCT00320268
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
600 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 31, 2006
Primary completion
Not listed
Completion
Apr 30, 2007
Last update posted
Mar 24, 2009

2006 – 2007

United States locations

U.S. sites
37
U.S. states
26
U.S. cities
37
Facility City State ZIP Site status
Research Site Little Rock Arkansas — —
Research Site Newport Beach California — —
Research Site Northridge California — —
Research Site Oceanside California — —
Research Site Santa Ana California — —
Research Site Denver Colorado — —
Research Site Norwich Connecticut — —
Research Site Washington D.C. District of Columbia — —
Research Site Jacksonville Florida — —
Research Site Winter Park Florida — —
Research Site Atlanta Georgia — —
Research Site Smyrna Georgia — —
Research Site Eagle Idaho — —
Research Site Oak Brook Illinois — —
Research Site Wichita Kansas — —
Research Site Shreveport Louisiana — —
Research Site Farmington Hills Michigan — —
Research Site St Louis Missouri — —
Research Site Las Vegas Nevada — —
Research Site Cherry Hill New Jersey — —
Research Site Clementon New Jersey — —
Research Site Brooklyn New York — —
Research Site New York New York — —
Research Site Staten Island New York — —
Research Site Raleigh North Carolina — —
Research Site Cincinnati Ohio — —
Research Site Tulsa Oklahoma — —
Research Site Portland Oregon — —
Research Site Norristown Pennsylvania — —
Research Site Memphis Tennessee — —
Research Site Austin Texas — —
Research Site Dallas Texas — —
Research Site San Antonio Texas — —
Research Site Bellevue Washington — —
Research Site Seattle Washington — —
Research Site Charleston West Virginia — —
Research Site Brown Deer Wisconsin — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00320268, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 24, 2009 · Synced Sep 27, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00320268 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →