Rationale and design of CONTINUITY: a Phase 4 randomized controlled trial of continued post-discharge sodium zirconium cyclosilicate treatment versus standard of care for hyperkalemia in chronic kidney disease

Author:

Burton James O12ORCID,Allum Alaster M3,Amin Alpesh4,Linde Cecilia5,Lesén Eva6,Mellström Carl7,Eudicone James M8,Sood Manish M9

Affiliation:

1. Department of Cardiovascular Sciences, University of Leicester and University , Leicester , UK

2. Hospitals of Leicester , Leicester , UK

3. Global Medical Affairs, Renal Medicine, AstraZeneca , Cambridge , UK

4. Department of Medicine, University of California Irvine , Irvine, CA , USA

5. Department of Medicine, Karolinska Institutet , Stockholm , Sweden

6. CVRM Evidence, AstraZeneca , Gothenburg , Sweden

7. BioPharmaceuticals CVRM, AstraZeneca , Gothenburg , Sweden

8. Medical and Payer Evidence Statistics, AstraZeneca , Wilmington, DE , USA

9. Ottawa Hospital Research Institute, The Ottawa Hospital , Ottawa , Canada

Abstract

ABSTRACT Background Individuals with chronic kidney disease (CKD) hospitalized with hyperkalemia are at risk of hyperkalemia recurrence and re-hospitalization. We present the rationale and design of CONTINUITY, a study to examine the efficacy of continuing sodium zirconium cyclosilicate (SZC)—an oral, highly selective potassium (K+) binder—compared with standard of care (SoC) on maintaining normokalemia and reducing re-hospitalization and resource utilization among participants with CKD hospitalized with hyperkalemia. Methods This Phase 4, randomized, open-label, multicenter study will enroll adults with Stage 3b–5 CKD and/or estimated glomerular filtration rate <45 mL/min/1.73 m2, within 3 months of eligibility screening, hospitalized with a serum potassium (sK+) level of >5.0–≤6.5 mmol/L, without ongoing K+ binder treatment. The study will include an in-hospital phase, where participants receive SZC for 2–21 days, and an outpatient (post-discharge) phase. At discharge, participants with sK+ 3.5–5.0 mmol/L will be randomized (1:1) to SZC or SoC and monitored for 180 days. The primary endpoint is the occurrence of normokalemia at 180 days. Secondary outcomes include incidence and number of hospital admissions or emergency department visits both with hyperkalemia as a contributing factor, and renin–angiotensin–aldosterone system inhibitor down-titration. The safety and tolerability of SZC will be evaluated. Ethics approval has been received from all relevant ethics committees. Enrollment started March 2022 and the estimated study end date is December 2023. Conclusions This study will assess the potential of SZC versus SoC in managing people with CKD and hyperkalemia post-discharge. Trial registration ClinicalTrials.gov identifier: NCT05347693; EudraCT: 2021-003527-14, registered on 19 October 2021.

Funder

AstraZeneca

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

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