Hexasodium fytate exposure-response correlations in a randomized, placebo-controlled study of patients on dialysis with cardiovascular calcification

Patients receiving dialysis have high cardiovascular risk in part due to extensive vascular calcification. In the CaLIPSO study, infusion of hexasodium fytate (SNF472), the hexasodium salt of inositol hexaphosphate, for 52 weeks thrice weekly during hemodialysis significantly reduced progression of...

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Published in:Frontiers in pharmacology 2024-02, Vol.15, p.1325186-1325186
Main Authors: Perelló, Joan, Alberti, Joan, Torres, Juan Vicente, Ferrer, Miguel D, Perez, M Mar, Bassissi, Firas, Gold, Alex, Raggi, Paolo, Chertow, Glenn M, Salcedo, Carolina
Format: Article
Language:English
Subjects:
calcification
cardiovascular
hexasodium fytate
pharmacodynamics
pharmacokinetics
Pharmacology
SNF472
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Summary:Patients receiving dialysis have high cardiovascular risk in part due to extensive vascular calcification. In the CaLIPSO study, infusion of hexasodium fytate (SNF472), the hexasodium salt of inositol hexaphosphate, for 52 weeks thrice weekly during hemodialysis significantly reduced progression of coronary artery calcification (CAC). This report examines pharmacokinetic/pharmacodynamic (PK/PD) and exposure-efficacy in CaLIPSO. We measured hexasodium fytate plasma concentrations (PK) by validated liquid chromatography-mass spectroscopy, and hydroxyapatite crystallization in plasma (PD) by validated spectrophotometry. Analyses included patients evaluable for PK, PD, and CAC change (per-protocol analysis). We developed a simple E model for maximum concentration (C ) and PD effect, and linear and non-linear E models for exposure-efficacy among individual average C and absolute and percent changes in CAC score from baseline to week 52. Among evaluable patients receiving placebo ( = 15), 300 mg ( = 20), or 600 mg ( = 20), average C across visits was not quantifiable (21.9 µM and a plateau in exposure-efficacy above the third quartile of C (≥32 µM). Hexasodium fytate has exposure-dependent effects on hydroxyapatite crystallization and progression of cardiovascular calcification. Simple E models show robust relations among exposure, inhibition of hydroxyapatite crystallization, and change in CAC volume. https://www.clinicaltrials.gov; identifier NCT02966028.
ISSN:1663-9812
1663-9812
DOI:10.3389/fphar.2024.1325186