Study identifier:D1443L00074
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A 3 weeks open label study to evaluate the efficacy in agitation and safety of Quetiapine fumarate XR in treatment of patients with acute schizophrenia
schizophrenia
Phase 4
No
Quetiapine XR (Seroquel XR)
All
35
Interventional
18 Years - 65 Years
Allocation: N/A
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Verified 01 Jan 2013 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
-
The purpose of the study is to determine whether treatment with quetiapine XR (Seroquel XR) tablets for 3 weeks will improve their agitation when they have acute psychosis.
Location
Location
Kuala Lumpur, Malaysia
Location
Johor, Johor Bahru, Malaysia
Arms | Assigned Interventions |
---|---|
Experimental: Quetiapine XR Quetiapine XR 300 mg on day 1, 600 mg on day 2, and 400-800 mg (at investigator's discretion) on day 3 and onwards. | Drug: Quetiapine XR (Seroquel XR) Tablet, oral, once daily Other Name: Seroquel XR |
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