Quetiapine Fumarate (SEROQUEL) Compared to Placebo in the Treatment of Children & Adolescents with Bipolar I Mania - ANCHOR 149
Study identifier:D1441C00149
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
Study Complete
Official Title
A 3-wk, Multicenter, Randomized, Double-blind, Parallel-group, Placebo-controlled, Phase 3b Study of the Efficacy & Safety of Quetiapine Fumarate (SEROQUEL™) Immediate-release Tablets in the Treatment of Children & Adolescents with Bipolar I Mania (abbreviated)
Medical condition
Bipolar Disorder
Phase
Phase 3
Healthy volunteers
No
Study drug
quetiapine fumarate
Sex
All
Actual Enrollment
220
Study type
Interventional
Age
10 Years - 17 Years
Date
Study Start Date: 01 Jul 2004
Primary Completion Date: -
Study Completion Date: 01 Jul 2006
Study design
Allocation: Randomized
Endpoint Classification: 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
Seroquel Medical Science Director
AstraZeneca
