drugset / Trial / NCT03781089

Patiromer Efficacy to Reduce Episodic Hyperkalemia in End Stage Renal Disease Patients

NCT03781089

Phase 4 Completed 36 enrolled Duke University Vifor Pharma · collab
RandomizedParallel-groupSingle-blindPrevention

Summary

The purpose of this study is to determine whether once-daily dosing of patiromer will reduce the frequency of hyperkalemic episodes in ESRD (end stage renal disease) study participants who receive conventional hemodialysis (HD). The study objective is to determine if patiromer administered orally once a day with breakfast or lunch will reduce episodes of hyperkalemia in ESRD study participants who receive thrice-weekly HD.

Timeline

Start
2019-06-20
Primary completion
2023-03-15
Completion
2023-03-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Patiromer Other / unclassified 8.4 g Oral