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A 24-week, Multicentre, Randomised, Double-Blind, Placebo-Controlled, Parallel-Group, International Phase III Study With 24 Week Extension to Evaluate the Safety and Efficacy of Dapagliflozin 10 mg/Day in Patients With Type 2 Diabetes Who Have Inadequate Glycemic Control on a DPP-4 Inhibitor Sitagliptin+/-Metformin
This study aims to investigate how dapagliflozin can control blood sugar in patients with type 2 diabetes when added to existing treatments (sitagliptin alone or in combination with metformin). The effect of dapagliflozin on weight and blood pressure will also be studied.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Research Site
Huntsville, Alabama, United States
Research Site
Ozark, Alabama, United States
Research Site
Anaheim, California, United States
Research Site
Chula Vista, California, United States
Research Site
Greenbrae, California, United States
Research Site
Laguna Hills, California, United States
Research Site
Los Angeles, California, United States
Research Site
Riverside, California, United States
Research Site
West Hills, California, United States
Research Site
Boca Raton, Florida, United States
Start Date
October 1, 2009
Primary Completion Date
March 1, 2011
Completion Date
September 1, 2011
Last Updated
June 13, 2014
833
ACTUAL participants
Dapagliflozin
DRUG
Placebo
DRUG
Lead Sponsor
AstraZeneca
Collaborators
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 ConditionsNCT06671587