Overview

Reducing Residual Albuminuria in Subjects With Diabetes and Nephropathy With Atrasentan

Status:
Completed
Trial end date:
2012-07-01
Target enrollment:
Participant gender:
Summary
Prospective, randomized, double-blind, placebo controlled, 12-week, multicenter study. The objective of the study is to evaluate the efficacy and safety of once daily administration of atrasentan tablets compared to placebo in reducing residual albuminuria in Japanese Type 2 diabetic patients with nephropathy who are treated with the maximum tolerated labeled dose for hypertension of a RAS (renin angiotensin system) inhibitor.
Phase:
Phase 2
Details
Lead Sponsor:
AbbVie (prior sponsor, Abbott)
Treatments:
Atrasentan
Endothelin Receptor Antagonists