drugset / Trial / NCT02345057

A Study to Evaluate Efficacy and Safety of CS-3150 in Japanese Type 2 Diabetic Subjects With Microalbuminuria

NCT02345057

Phase 2 Completed 365 enrolled Daiichi Sankyo
RandomizedParallel-groupQuadruple-blindTreatment

Summary

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).

Timeline

Start
2015-01
Primary completion
2016-06
Completion
2016-07

Drugs

EvaluationDrugModalityDoseRoute
Subject CS-3150 Unknown 0.625 mg Oral
Subject CS-3150 Unknown 1.25 mg Oral
Subject CS-3150 Unknown 2.5 mg Oral
Subject CS-3150 Unknown 5 mg Oral