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SNF472: mechanism of action and results from clinical trials.
Sinha, Smeeta; Raggi, Paolo; Chertow, Glenn M.
Afiliação
  • Sinha S; Department of Renal Medicine, Salford Royal NHS Foundation Trust, and University of Manchester, Manchester, UK.
  • Raggi P; Division of Cardiology and Department of Medicine, University of Alberta, Edmonton, AB, Canada.
  • Chertow GM; Department of Medicine, Stanford University School of Medicine, Palo Alto, California, USA.
Curr Opin Nephrol Hypertens ; 30(4): 424-429, 2021 07 01.
Article em En | MEDLINE | ID: mdl-34027904
PURPOSE OF REVIEW: Vascular calcification (VC) is associated with increased cardiovascular event rates, particularly in patients with end-stage kidney disease (ESKD). Dysregulated mineral metabolism and inflammation have been shown to promote VC, however, treatment options targeting VC specifically are not available. This review outlines the pathophysiological mechanisms contributing to VC in ESKD and describes recent studies evaluating the effects of the first-in-class inhibitor of VC, SNF472. RECENT FINDINGS: SNF472 directly inhibits calcium phosphate crystal formation and aggregation. SNF472 has completed early phase clinical trials with a favourable safety profile and Phase 2 clinical trial data have shown attenuation of coronary artery and aortic valve calcification in patients receiving hemodialysis. SUMMARY: Therapeutic agents that directly target VC may prevent the multiple complications associated with dystrophic calcification in patients with ESKD.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Calcificação Vascular / Falência Renal Crônica Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Calcificação Vascular / Falência Renal Crônica Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article