This study is a randomized, placebo-controlled, double-blind, multi-center study to evaluate efficacy and safety of different doses of CS-3150 compared to placebo in Japanese Type 2 Diabetes Mellitus and Microalbuminuria. The Primary endpoint is the change from baseline in urinary albumin to creatine ratio (UACR).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
365
Unnamed facility
Kumamoto, Japan
Change from baseline in urinary albumin to creatine ratio (UACR)
Time frame: Baseline to end of Week 12
Transition from microalbuminuria to normoalbuminuria
Time frame: Baseline to end of Week 12
Change in renal function
Time frame: Baseline to end of Week 12
Change in serum potassium
Time frame: Baseline to end of Week 12
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