drugset / Trial / NCT01130597

Evaluation of Patiromer Titration in Heart Failure Patients With Chronic Kidney Disease

NCT01130597

Phase 2 Completed 63 enrolled Relypsa, Inc.
NaSingle-groupOpen-labelPrevention

Summary

The purpose of this study was to evaluate the feasibility of individualized titration of patiromer according to serum potassium. This study also assessed the safety and tolerability of patiromer and the effects of patiromer on serum potassium in heart failure (HF) participants with chronic kidney disease (CKD).

Timeline

Start
2010-05
Primary completion
2010-09
Completion
2010-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Patiromer Other / unclassified 20 g
Background Spironolactone Small molecule 50 mg

Indications