SR-Registration Study 1, ROW: Efficacy and Safety of Seroquel® in the Treatment of Patients With Schizophrenia
Study identifier:D1444C00132
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
Study Complete
Official Title
A 6-week, Multicenter, Double-blind, Double-dummy, Randomized Comparison of the Efficacy & Safety of Sustained-Release Formulation Quetiapine Fumarate (SEROQUEL) & Placebo in the Treatment of Acutely Ill Patients with Schizophrenia
Medical condition
Schizophrenic disorder
Phase
Phase 3
Healthy volunteers
No
Study drug
Seroquel Sustained Release (SR), Seroquel Immediate Release (IR), Placebo
Sex
All
Actual Enrollment
535
Study type
Interventional
Age
18 Years - 65 Years
Date
Study Start Date: 01 Nov 2004
Primary Completion Date: -
Study Completion Date: 01 Dec 2005
Study design
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment
Verification:
Verified 01 Nov 2013 by AstraZeneca
Sponsors
AstraZeneca
Collaborators
-
Inclusion and exclusion criteria
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No locations available
| Arms | Assigned Interventions |
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Contacts
Investigators
Principal Investigator
AstraZeneca CNS Medical Science Director
AstraZeneca
