Study identifier:D1692C00013
ClinicalTrials.gov identifier:NCT02157298
EudraCT identifier:N/A
CTIS identifier:N/A
A 16-week multicenter, randomized, parallel-group, double-blind, placebo-controlled Phase IV study with a 36-week extension period to evaluate the efficacy and safety of dapagliflozin therapy when added to the therapy of Japanese patients with type 2 diabetes with inadequate glycemic control on insulin
Type 2 Diabetes Mellitus
Phase 4
No
Dapagliflozin 5 mg, Placebo tablet
All
266
Interventional
20 Years - 130 Years
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment
Verified 01 Mar 2016 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: dapagliflozin 5mg dapagliflozin tablet 5mg | Drug: Dapagliflozin 5 mg Dapagliflozin, a blood glucose lowering drug. Oral dose |
Placebo Comparator: Placebo dapagliflozin tablet 5mg placebo | Drug: Placebo tablet Placebo tablet. Oral dose |