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  • A 24-week, multicentre, randomised, double-blind,age-stratified, placebo controlled phase III study with an 80-week extension period to evaluate the efficacy and safety of dapagliflozin 10 mg /day in patients with T2DM and cardiovascular disease, who exhibit inadequate glycaemic control on usual care

Disease
diabetes mellitus
Drug Name
dapagliflozin
Generic Name
dapagliflozin
Sponsor
AstraZeneca
Drug Status
Approved Medicine
Phase
IIIa
Start Date
Mar 15, 2010
Study Name
D1690C00019
Study Id
D1690C00019
ClinicalTrials.gov ID
NCT01042977
Recruiting Status
Closed
Protocol Status
Not Available
Report
Oct 13, 2011
  • D1690C00019.pdf (197 KB)

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