Clinical Trials Directory

Trials / Completed

CompletedNCT02517320

Efficacy and Safety of MT-3995 in Patients With Diabetic Nephropathy

A Randomized, Double-blind, Placebo-controlled Study to Evaluate Efficacy and Safety of MT-3995 in Patients With Diabetic Nephropathy

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
293 (actual)
Sponsor
Tanabe Pharma Corporation · Industry
Sex
All
Age
20 Years – 75 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
DRUGMT-3995 Low
DRUGMT-3995 Middle
DRUGMT-3995 High
DRUGPlacebo

Timeline

Start date
2015-07-01
Primary completion
2016-11-01
Completion
2017-01-01
First posted
2015-08-07
Last updated
2017-03-03

Locations

1 site across 1 country: Japan

Source: ClinicalTrials.gov record NCT02517320. Inclusion in this directory is not an endorsement.

Efficacy and Safety of MT-3995 in Patients With Diabetic Nephropathy (NCT02517320) · Clinical Trials Directory