Tenapanor: A Phosphate Absorption Inhibitor for the Management of Hyperphosphatemia in Patients with Kidney Failure.

Chronic kidney disease dialysis hyperphosphatemia serum phosphate tenapanor

Journal

Journal of renal nutrition : the official journal of the Council on Renal Nutrition of the National Kidney Foundation
ISSN: 1532-8503
Titre abrégé: J Ren Nutr
Pays: United States
ID NLM: 9112938

Informations de publication

Date de publication:
09 Jul 2024
Historique:
received: 16 04 2024
accepted: 01 07 2024
medline: 12 7 2024
pubmed: 12 7 2024
entrez: 11 7 2024
Statut: aheadofprint

Résumé

Because of increased risks of cardiovascular disease and death, patients with hyperphosphatemia receiving maintenance dialysis are advised to limit phosphorus consumption and are prescribed phosphate binders in an effort to better control serum phosphate concentrations. Because of large pill size, pill burden, and tolerability issues, phosphate binder adherence is relatively poor. On ingestion, phosphate is absorbed from the intestine via transcellular or paracellular transport. Data show that inhibiting sodium-hydrogen exchanger 3 modulates paracellular phosphate absorption (the predominant pathway in humans). Tenapanor is a first-in-class, minimally absorbed, phosphate absorption inhibitor that selectively inhibits sodium-hydrogen exchanger 3, with a mechanism distinct from, and complementary to, that of phosphate binders. In phase 3 and postregistrational studies, tenapanor conferred statistically significant and clinically meaningful reductions in serum phosphate in patients receiving maintenance dialysis with hyperphosphatemia. Here, we review the available preclinical and clinical data on the effects of tenapanor on controlling intestinal phosphate absorption.

Identifiants

pubmed: 38992521
pii: S1051-2276(24)00156-0
doi: 10.1053/j.jrn.2024.07.003
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Auteurs

Kathleen M Hill Gallant (KM)

Associate Professor, University of Minnesota, Saint Paul, MN. Electronic address: hillkm@umn.edu.

Stuart M Sprague (SM)

Clinical Professor of Medicine, Endeavor Health, University of Chicago, Evanston, IL.

David P Rosenbaum (DP)

Chief Development Officer, Ardelyx, Inc., Waltham, Massachusetts.

David M Spiegel (DM)

Vice President, Nephrology, Ardelyx, Inc., Waltham, Massachusetts.

Kenji Kozuka (K)

Director, Preclinical Research and Nonclinical Development, Ardelyx, Inc., Waltham, Massachusetts.

Susan Edelstein (S)

Senior Vice President, Clinical Research, Ardelyx, Inc., Fremont, California.

Glenn M Chertow (GM)

Professor of Medicine - Nephrology, Departments of Medicine and Epidemiology and Population Health, Stanford University, Palo Alto, CA.

Classifications MeSH