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A Phase IV, Multi-center, Double-blind, Double-dummy, Randomized, Parallel-group Study to Compare the Tolerability of Quetiapine Fumarate Immediate Release (Seroquel IR) With Quetiapine Fumarate Extended Release (Seroquel XR) During Initial Dose Escalation in Patients With Bipolar Depression
The purpose of the study is to compare the sedation profile one hour after dose administration between Seroquel IR and Seroquel XR.
Age
18 - 50 years
Sex
ALL
Healthy Volunteers
No
Start Date
June 1, 2009
Primary Completion Date
August 1, 2009
Completion Date
August 1, 2009
Last Updated
May 11, 2011
139
ACTUAL participants
Quetiapine Immediate Release
DRUG
Quetiapine Extended Release
DRUG
Lead Sponsor
AstraZeneca
NCT04480918
NCT06524505
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07172516