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The hepatocyte growth factor mimetic, ANG-3777, in kidney transplant recipients with delayed graft function: Results from a randomized phase 3 trial.
Vincenti, Flavio; Bromberg, Jonathan; Kim, Jim; Faravardeh, Arman; Leca, Nicolae; Alperovich, Gabriela; Csomor, Philipp Andreas; Aslam, Shakil; Neylan, John.
Afiliação
  • Vincenti F; Department of Medicine, University of California San Francisco, San Francisco, California, USA. Electronic address: flavio.vincenti@ucsf.edu.
  • Bromberg J; Division of Transplant Surgery, Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Kim J; Department of Surgery, University of Southern California, Los Angeles, California, USA.
  • Faravardeh A; Sharp HealthCare Kidney and Pancreas Transplant Center, San Diego, California, USA.
  • Leca N; Department of Medicine, University of Washington Medical Center, Seattle, Washington, USA.
  • Alperovich G; CSL Vifor, Madrid, Spain.
  • Csomor PA; CSL Vifor, Zurich, Switzerland.
  • Aslam S; Angion Biomedica, New York, New York, USA.
  • Neylan J; Angion Biomedica, New York, New York, USA.
Am J Transplant ; 2024 Feb 20.
Article em En | MEDLINE | ID: mdl-38387622
ABSTRACT
In kidney transplant recipients, delayed graft function increases the risk of graft failure and mortality. In a phase 3, randomized, double-blind, placebo-controlled trial, we investigated the hepatocyte growth factor mimetic, ANG-3777 (once daily for 3 consecutive days, starting ≤30 hours posttransplant), in 248 patients receiving a first kidney transplant from a deceased donor. At day 360, estimated glomerular filtration rate (primary endpoint) was not significantly different between the ANG-3777 and placebo groups. There were no significant between-group differences in the duration of dialysis through day 30 or in the percentage of patients with an estimated glomerular filtration rate of >30 mL/min/1.73 m2 at day 360. The incidence of both delayed graft function and acute rejection was similar between ANG-3777 and placebo groups (68.5% vs 69.4% and 8.1% vs 6.5%, respectively). ANG-3777 was well tolerated, and there was a numerically lower incidence of graft failure versus placebo (3.2% vs 8.1%). Although there is insufficient evidence to support an indication of ANG-3777 for patients at risk of renal dysfunction after deceased-donor kidney transplantation, these findings indicate potential biological activity that may warrant further investigation.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Am J Transplant Assunto da revista: TRANSPLANTE Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Am J Transplant Assunto da revista: TRANSPLANTE Ano de publicação: 2024 Tipo de documento: Article