Sodium Zirconium Cyclosilicate in CKD, Hyperkalemia, and Metabolic Acidosis

Author:

Ash Stephen R.1ORCID,Batlle Daniel2ORCID,Kendrick Jessica3ORCID,Oluwatosin Yemisi4ORCID,Kooienga Laura5,Eudicone James M.6ORCID,Sundin Anna-Karin7ORCID,Guerrieri Emily8,Fried Linda F.9

Affiliation:

1. Nephrology Department, Indiana University Health Arnett, Lafayette, Indiana

2. Division of Nephrology and Hypertension, Department of Medicine, The Feinberg School of Medicine, Northwestern University, Chicago, Illinois

3. Division of Renal Diseases and Hypertension, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado

4. Renal CVRM (US Medical), AstraZeneca, Wilmington, Delaware

5. Colorado Kidney Care, Denver, Colorado

6. BioPharmaceuticals Medical (Evidence), AstraZeneca, Wilmington, Delaware

7. BioPharmaceuticals Medical (Evidence), AstraZeneca, Mölndal, Sweden

8. Renal CVRM, AstraZeneca, Gaithersburg, Maryland

9. Renal Section, Veterans Affairs Pittsburgh Healthcare System and Renal-Electrolyte Division, University of Pittsburgh, Pittsburgh, Pennsylvania

Abstract

Key Points Sodium zirconium cyclosilicate effectively lowers serum potassium and maintains normokalemia in patients with CKD with concomitant hyperkalemia and metabolic acidosis.Despite high screen failure and small sample size, a nominally significant increase in sHCO3 was seen for sodium zirconium cyclosilicate versus placebo.Further studies on the basis of an appropriate cohort size may help validate the trend observed in sHCO3 levels, supporting these clinically relevant findings. Background Metabolic acidosis and hyperkalemia are common in CKD. A potential dual effect of sodium zirconium cyclosilicate (SZC), a selective binder of potassium in the gastrointestinal tract, on serum potassium (sK+) and serum bicarbonate (sHCO3 ) was evaluated in patients with hyperkalemia and metabolic acidosis associated with CKD. Methods In the NEUTRALIZE study (NCT04727528), non-dialysis patients with stage 3–5 CKD, hyperkalemia (sK+>5.0 to ≤5.9 mmol/L), and metabolic acidosis (sHCO3 16–20 mmol/L) received open-label SZC 10 g three times daily for ≤48 hours. Patients achieving normokalemia (sK+ 3.5–5.0 mmol/L) were randomized 1:1 to SZC 10 g or placebo daily for 4 weeks. The primary end point was patients (%) maintaining normokalemia at the end of treatment (EOT) without rescue. Secondary end points included mean change in sHCO3 at EOT (day 29) and patients (%) with normokalemia with a ≥3-mmol/L increase in sHCO3 without rescue. Results Of 229 patients screened, 37 were randomized (SZC, n=17; placebo, n=20). High screen failure led to early study termination. At EOT, 88.2% (SZC) versus 20.0% (placebo) of patients maintained normokalemia (odds ratio, 56.2; P = 0.001). Low enrollment rendered secondary end point P values nominal. SZC treatment provided nominally significant increases in sHCO3 versus placebo from day 15 onward. Patients with normokalemia with a ≥3-mmol/L increase in sHCO3 without rescue were 35.3% (SZC) and 5.0% (placebo; P < 0.05). No new safety concerns were reported. Conclusions SZC effectively lowered sK+ and maintained normokalemia, with nominally significant increases in sHCO3 observed for SZC versus placebo.

Funder

This work was supported by AstraZeneca

Publisher

Ovid Technologies (Wolters Kluwer Health)

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