LivingGLP1
Study S002424

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

Registration

Registration
NCT02157298
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE4
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
266
Start
2014-06
Primary completion
2015-02
Lead sponsor
AstraZeneca
Conditions
Type 2 Diabetes Mellitus
Interventions
DRUG:Dapagliflozin 5 mg; DRUG:Placebo tablet
Results posted
TRUE

Registered primary outcomes

  • Adjusted Mean Change in HbA1c Levels [Baseline to Week 16]

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