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Completed Phase 3 Interventional

Efficacy & Safety of Quetiapine Fumarate (SEROQUEL) & Placebo in the Treatment of Acutely Ill Patients With Schizophrenia

ClinicalTrials.gov ID: NCT00085891

Public ClinicalTrials.gov record NCT00085891. 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 Nov 6, 2026, 12:40 PM EST

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Official title

A 6-Week, Multicenter, Double-Blind, Double-Dummy, Randomized Comparison of the Efficacy and Safety of Sustained-Release Formulation Quetiapine Fumarate (SEROQUEL) and Placebo in the Treatment of Acutely Ill Patients With Schizophrenia

Brief summary

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

The purpose of this study is to demonstrate superior efficacy of sustained release quetiapine compared to placebo in patients with schizophrenia after receiving treatment for up to 6 weeks.

Study identification

NCT ID
NCT00085891
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
535 participants

Conditions and interventions

Conditions

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
Jun 2004 (Type not available)
Primary completion
Not listed
Completion
Sep 2005 (Actual)
Last update posted
Mar 25, 2009

2004 – 2005

United States locations

U.S. sites
29
U.S. states
19
U.S. cities
29
Facility City State ZIP Site status
Research Site Birmingham Alabama — —
Research Site Cerritos California — —
Not listed Los Angeles California — —
Research Site San Diego California — —
Research Site Santa Ana California — —
Research Site Washington D.C. District of Columbia — —
Research Site Miami Florida — —
Not listed Oak Brook Illinois — —
Research Site Oakbrook Terrace Illinois — —
Research Site New Orleans Louisiana — —
Research Site Rockville Maryland — —
Not listed Brighton Massachusetts — —
Research Site Jackson Mississippi — —
Research Site St Louis Missouri — —
Research Site Holliswood New York — —
Research Site Lawrence New York — —
Research Site Staten Island New York — —
Research Site Medina Ohio — —
Research Site Oklahoma City Oklahoma — —
Research Site Norristown Pennsylvania — —
Research Site Philadelphia Pennsylvania — —
Research Site Sioux Falls South Dakota — —
Research Site Memphis Tennessee — —
Research Site Austin Texas — —
Research Site Houston Texas — —
Research Site Irving Texas — —
Research Site San Antonio Texas — —
Research Site Richmond Virginia — —
Research Site Kirkland Washington — —

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 NCT00085891, 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 25, 2009 · Synced Nov 6, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00085891 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →