Efficacy and safety of sodium zirconium cyclosilicate for hyperkalaemia: the randomized, placebo‐controlled HARMONIZE‐Global study

  • Faiez Zannad
    Université de Lorraine, Inserm, Centre d'Investigation Clinique 1433 and Centre Hospitalier Universitaire Nancy France
  • Bang‐Gee Hsu
    Division of Nephrology Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation Hualien Taiwan
  • Yoshitaka Maeda
    Nephrology Division, Department of Internal Medicine JA Toride Medical Center Ibaraki Japan
  • Sug Kyun Shin
    NHIS Medical Center Ilsan Hospital Goyang‐si Gyeonggi‐do South Korea
  • Elena M. Vishneva
    City Clinical Hospital No. 14 Ekaterinburg Russian Federation
  • Martin Rensfeldt
    Biometrics, Late‐Stage Development, Cardiovascular, Renal and Metabolism (CVRM), BioPharmaceuticals R&D AstraZeneca Gothenburg Mölndal Sweden
  • Stefan Eklund
    AstraZeneca Gothenburg Mölndal Sweden
  • June Zhao
    AstraZeneca Gaithersburg MD USA

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<jats:title>Abstract</jats:title><jats:sec><jats:title>Aims</jats:title><jats:p>Sodium zirconium cyclosilicate (SZC, formerly ZS‐9) is a selective K<jats:sup>+</jats:sup> binder to treat adults with hyperkalaemia. HARMONIZE‐Global examined the efficacy and safety of SZC among outpatients with hyperkalaemia from diverse geographic and ethnic origins.</jats:p></jats:sec><jats:sec><jats:title>Methods and results</jats:title><jats:p>This phase 3, randomized, double‐blind, placebo‐controlled study recruited outpatients with serum K<jats:sup>+</jats:sup> ≥5.1 mmol/L (measured by point‐of‐care i‐STAT device) at 45 sites in Japan, Russia, South Korea, and Taiwan. Following open‐label treatment with thrice‐daily SZC 10 g during a 48 h correction phase (CP), patients achieving normokalaemia (K<jats:sup>+</jats:sup> 3.5–5.0 mmol/L) were randomized 2:2:1 to once‐daily SZC 5 g, SZC 10 g, or placebo during a 28 day maintenance phase (MP). The primary endpoint was mean central‐laboratory K<jats:sup>+</jats:sup> level during days 8–29 of the MP. Of 267 patients in the CP, 248 (92.9%) entered the MP. During the CP, mean central‐laboratory K<jats:sup>+</jats:sup> was reduced by 1.28 mmol/L at 48 h vs. baseline (<jats:italic>P</jats:italic> < 0.001). During the MP (days 8–29), SZC 5 and 10 g once‐daily significantly lowered mean central‐laboratory K<jats:sup>+</jats:sup> by 9.6% and 17.7%, respectively, vs. placebo (<jats:italic>P</jats:italic> < 0.001 for both). More patients had normokalaemia (central‐laboratory K<jats:sup>+</jats:sup> 3.5–5.0 mmol/L at day 29) with SZC 5 (58.6%) and 10 g (77.3%) vs. placebo (24.0%), with the greatest number of normokalaemic days in the 10‐g group. The most common adverse events with SZC were mild or moderate constipation and oedema.</jats:p></jats:sec><jats:sec><jats:title>Conclusions</jats:title><jats:p>Normokalaemia achieved during the CP was maintained over 28 days with SZC treatment among outpatients with hyperkalaemia.</jats:p></jats:sec>

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