drugset / Trial / NCT03888066

Patiromer for the Management of Hyperkalemia in Subjects Receiving RAASi Medications for the Treatment of Heart Failure (DIAMOND)

NCT03888066 ↗

Phase 3 Completed 1195 enrolled Vifor Pharma Syneos Health · collab
RandomizedParallel-groupQuadruple-blindPrevention

Summary

The purpose of this study is to assess the effects of patiromer compared with placebo on serum K+ in HF patients.

Timeline

Start
2019-04-24
Primary completion
2021-09-02
Completion
2021-09-02

Outcome

Met primary endpoint

registry analysis (superiority test); Patiromer vs Placebo; p < 0.001; Mean Difference (Final Values) -0.097 (95% CI -0.128 to -0.067) NCT03888066 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Patiromer Other / unclassified 0 unknown —
Subject Patiromer Other / unclassified 1 unknown —
Subject Patiromer Other / unclassified 2 unknown —
Subject Patiromer Other / unclassified 3 unknown —

Indications

No indication recorded.