drugset / Trial / NCT02088073

Safety & Efficacy of Zirconium Silicate Dosed for 28 Days in Hyperkalemia.

NCT02088073 ↗

Phase 3 Completed 258 enrolled ZS Pharma, Inc.
RandomizedParallel-groupQuadruple-blindSupportive care

Summary

It is hypothesized that ZS is more effective than placebo control (alternative hypothesis) in maintaining mean double-blind randomized maintenance phase (DBRMP) Day 8-29 serum potassium levels (3.5 - 5.0 mmol/l, inclusive) among hyperkalemic subjects in whom normokalemia was established during the open-label acute phase versus no difference between each ZS dose (highest to lowest) versus placebo control (null hypothesis).

Timeline

Start
2014-03-31
Primary completion
2014-08-31
Completion
2015-01-31

Outcome

Met primary endpoint

paper In the randomized phase, serum potassium was significantly lower during days 8-29 with all 3 zirconium cyclosilicate doses vs placebo. PMID 25402495 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Sodium Zirconium Cyclosilicate Other / unclassified 5 g —
Subject Sodium Zirconium Cyclosilicate Other / unclassified 10 g —
Subject Sodium Zirconium Cyclosilicate Other / unclassified 15 g —

Indications

No indication recorded.