Viewing Study NCT00422214



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Study NCT ID: NCT00422214
Status: COMPLETED
Last Update Posted: 2009-03-25
First Post: 2007-01-12

Brief Title: Phase IIISeroquel SR Bipolar Depression Monotherapy - US
Sponsor: AstraZeneca
Organization: AstraZeneca

Study Overview

Official Title: A Multicenter Double-Blind Randomized Parallel-Group Placebo-Controlled Phase III Study of the Efficacy and Safety of Quetiapine Fumarate Seroquel SR Sustained-Release as Monotherapy in Adult Patients With Acute Bipolar Depression
Status: COMPLETED
Status Verified Date: 2009-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to determine the safety and efficacy of sustained-release quetiapine fumarate Seroquel in the treatment of patients with Acute Bipolar Depression for 8 weeks

PLEASE NOTE Seroquel SR and Seroquel XR refer to the same formulation The SR designation was changed to XR after consultation with FDA
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None