Overview

A Study to Investigate the Safety and Efficacy of ZS in Patients With Hyperkalemia

Status:
Completed
Trial end date:
2018-02-14
Target enrollment:
Participant gender:
Summary
To evaluate the efficacy of two different doses (5 and 10 g) of ZS orally administered once daily (qd) vs placebo in maintaining normokalemia in initially hyperkalemic patients having achieved normokalemia following two days of initial ZS therapy (10g TID).
Phase:
Phase 3
Details
Lead Sponsor:
AstraZeneca