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Anticoagulation with osocimab in patients with kidney failure undergoing hemodialysis: a randomized phase 2 trial.
Weitz, Jeffrey I; Tankó, László B; Floege, Jürgen; Fox, Keith A A; Bhatt, Deepak L; Thadhani, Ravi; Hung, James; Pap, Ákos F; Kubitza, Dagmar; Winkelmayer, Wolfgang C.
Afiliação
  • Weitz JI; Thrombosis and Atherosclerosis Research Institute and McMaster University, Hamilton, Ontario, Canada. weitzj@taari.ca.
  • Tankó LB; Clinical Development and Operations, Bayer Consumer Care AG, Basel, Switzerland.
  • Floege J; Division of Nephrology and Rheumatology, RWTH Aachen University Hospital, Aachen, Germany.
  • Fox KAA; Centre for Cardiovascular Sciences, University of Edinburgh, Edinburgh, UK.
  • Bhatt DL; Mount Sinai Heart, Icahn School of Medicine at Mount Sinai Health System, New York, NY, USA.
  • Thadhani R; Emory University School of Medicine, Atlanta, GA, USA.
  • Hung J; Clinical Development and Operations, Bayer SA, São Paulo, Brazil.
  • Pap ÁF; Clinical Data Sciences and Analytics, Bayer AG, Wuppertal, Germany.
  • Kubitza D; Clinical Pharmacology, Bayer AG, Wuppertal, Germany.
  • Winkelmayer WC; Section of Nephrology, Baylor College of Medicine, Houston, TX, USA.
Nat Med ; 30(2): 435-442, 2024 Feb.
Article em En | MEDLINE | ID: mdl-38365952
ABSTRACT
Individuals with kidney failure undergoing hemodialysis are at elevated risk for thromboembolic events. Factor (F) XI, which is in the intrinsic pathway of coagulation, is emerging as an attractive target for new anticoagulants that may be safer than existing agents. Osocimab-an inhibitory FXIa antibody-is a potential treatment option for such patients. We conducted a phase 2b, double-blind, placebo-controlled trial, in which 704 participants (448 male, 256 female) with kidney failure undergoing hemodialysis were randomized to receive lower- or higher-dose osocimab or placebo. In total, 686 participants (436 male, 250 female) received treatment for ≤18 months (planned minimal treatment period of 6 months). The co-primary outcomes were clinically relevant bleeding (a composite of major and clinically relevant nonmajor bleeding) and a composite of the incidence of moderate, severe or serious adverse events. Clinically relevant bleeding occurred in 16/232 (6.9%) and 11/224 (4.9%) participants who received lower- and higher-dose osocimab, respectively, and in 18/230 participants (7.8%) who received a placebo. For the composite adverse event endpoint, incidences were 51%, 47% and 43% in the lower-dose osocimab, higher-dose osocimab and placebo groups, respectively. These results suggest that osocimab is associated with a low risk of bleeding and is generally well tolerated in this population; findings that require confirmation in larger trials. ClinicalTrials.gov identifier, NCT04523220 .
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Coagulação Sanguínea / Insuficiência Renal / Anticorpos Monoclonais Humanizados Limite: Female / Humans / Male Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Coagulação Sanguínea / Insuficiência Renal / Anticorpos Monoclonais Humanizados Limite: Female / Humans / Male Idioma: En Ano de publicação: 2024 Tipo de documento: Article