drugset / Trial / NCT01858532

Study Of Diabetic Nephropathy With Atrasentan

NCT01858532

Phase 3 Terminated 5107 enrolled AbbVie
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The study objective was to evaluate the effect of atrasentan compared with placebo on time to doubling of serum creatinine (DBSC) or the onset of end-stage renal disease (ESRD) in participants with type 2 diabetes and nephropathy who were treated with the maximum tolerated labeled daily dose (MTLDD) of a renin-angiotensin system (RAS) inhibitor. In addition, the study assessed the effects of atrasentan compared with placebo on cardiovascular (CV) morbidity and mortality, urine albumin excretion, changes in estimated glomerular filtration rate (eGFR), as well as the impact on quality of life in participants with type 2 diabetes and nephropathy.

Timeline

Start
2013-05-17
Primary completion
2018-03-29
Completion
2018-03-29

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Atrasentan Other / unclassified 0.75 mg Oral