drugset / Trial / NCT01424319

Reducing Residual Albuminuria in Subjects With Diabetes and Nephropathy With Atrasentan

NCT01424319 ↗

Phase 2 Completed 58 enrolled AbbVie
RandomizedParallel-groupQuadruple-blindTreatment

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.

Timeline

Start
2011-08
Primary completion
2012-07
Completion
2012-07

Outcome

Met primary endpoint

paper Compared with placebo, 0.75 mg and 1.25 mg atrasentan reduced urine albumin/creatinine ratios by an average of 35% and 38% PMID 24722445 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Atrasentan Other / unclassified 0.75 mg Oral
Subject Atrasentan Other / unclassified 1.25 mg Oral