drugset / Trial / NCT00573430

ARIA (Atacand Renoprotection In NephropAthy Pt.)

NCT00573430

Phase 4 Completed 128 enrolled AstraZeneca
RandomizedParallel-groupOpen-labelTreatment

Summary

To determine the effective dose of candesartan cilexetil for reduction of urinary protein excretion in hypertensive patients with non-diabetic chronic kidney disease with baseline urinary protein/creatinine ratio between 500mg/g and 5000mg/g, by assessing the change in urinary protein/creatinine ratio from baseline to the end of 28-week treatment

Timeline

Start
2007-12
Primary completion
2009-08
Completion
2009-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Candesartan cilexetil Unknown 8 mg Oral
Subject Candesartan cilexetil Unknown 16 mg Oral
Subject Candesartan cilexetil Unknown 32 mg Oral