drugset / Trial / NCT01737697

Safety & Efficacy of Zirconium Silicate in Mild to Moderate Hyperkalemia

NCT01737697

Phase 3 Completed 754 enrolled ZS Pharma, Inc.
RandomizedParallel-groupQuadruple-blindSupportive care

Summary

Acute Phase: It is hypothesized that ZS (zirconium silicate) is more effective than placebo control (alternative hypothesis) in lowering S-K levels in subjects with S-K between 5.0 - 6.5 mmol/l versus no difference between ZS and placebo control (null hypothesis). Subacute Phase (randomized withdrawal): It is hypothesized that ZS once daily is more effective than placebo control (alternative hypotheses) in maintaining normokalemic levels (3.5 - 4.9 mmol/l) among subjects completing the Acute Phase versus no difference between each ZS dose and respective placebo controls (null hypotheses).

Timeline

Start
2012-11-30
Primary completion
2013-10-31
Completion
2013-11-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Sodium Zirconium Cyclosilicate Other / unclassified 1.25 g Oral
Subject Sodium Zirconium Cyclosilicate Other / unclassified 2.5 g Oral
Subject Sodium Zirconium Cyclosilicate Other / unclassified 5 g Oral
Subject Sodium Zirconium Cyclosilicate Other / unclassified 10 g Oral

Indications

No indication recorded.