The purpose of this study is to evaluate the efficacy of MT-3995 in subjects with diabetic nephropathy, compared with placebo, using urine albumin- to-creatinine ratio (UACR) in the first morning void urine sample as an indicator.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
293
Investigational site
Hokkaido, Japan
Change form baseline in UACR
Time frame: Week 24
Change in UACR classification
Time frame: From baseline to 24 weeks
Change in renal function
Time frame: From baseline to 24 weeks
Change in serum potassium
Time frame: From baseline to 24 weeks
Adverse events
Time frame: From baseline to 24 weeks
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