Proteinuria as an Endpoint in Clinical Trials of Focal Segmental Glomerulosclerosis.

clinical trials focal segmental glomerulosclerosis (FSGS) proteinuria surrogate endpoints

Journal

American journal of kidney diseases : the official journal of the National Kidney Foundation
ISSN: 1523-6838
Titre abrégé: Am J Kidney Dis
Pays: United States
ID NLM: 8110075

Informations de publication

Date de publication:
23 Oct 2024
Historique:
received: 29 05 2024
revised: 26 07 2024
accepted: 11 08 2024
medline: 26 10 2024
pubmed: 26 10 2024
entrez: 25 10 2024
Statut: aheadofprint

Résumé

Focal Segmental Glomerulosclerosis (FSGS) is a characteristic histopathological lesion that is indicative of underlying glomerular dysfunction. It is not a single disease entity but rather a heterogeneous disorder that is an important cause of nephrotic syndrome and kidney failure in children and adults. The aim of this Kidney Health Initiative project was to evaluate potential endpoints for clinical trials in FSGS. This paper focuses on the data supporting proteinuria as a surrogate endpoint. Available data support the use of complete remission of proteinuria in patients with heavy proteinuria as a surrogate endpoint for progression to kidney failure. While substantial treatment effects on proteinuria that are short of a complete remission may also predict the effect of a treatment on progression to kidney failure, further work is needed to determine how such an endpoint should be defined. Fortunately, efforts are underway to bring together patient-level data from randomized controlled trials, observational studies, and registries to address this issue.

Identifiants

pubmed: 39455047
pii: S0272-6386(24)01038-2
doi: 10.1053/j.ajkd.2024.08.011
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Auteurs

Laura H Mariani (LH)

University of Michigan Renal Division, Ann Arbor, MI, USA. Electronic address: lmariani@umich.edu.

Howard Trachtman (H)

University of Michigan, Department of Pediatrics/Nephrology, Ann Arbor, MI, USA. Electronic address: howardtrachtman21@gmail.com.

Aliza Thompson (A)

Center for Drug Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, MD, USA.

Barbara S Gillespie (BS)

Fortrea, Durham, NC, University of North Carolina Kidney Center, Chapel Hill, NC, USA.

Michelle Denburg (M)

The Children's Hospital of Philadelphia, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.

Ulysses Diva (U)

Travere Therapeutics, San Diego, CA, USA.

Duvuru Geetha (D)

Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Peter J Greasley (PJ)

Research and Early Development, Cardiovascular, Renal and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg.

Michelle A Hladunewich (MA)

University of Toronto, Toronto, Ontario, Canada.

Robert B Huizinga (RB)

Aurinia Pharmaceuticals, Victoria, British Columbia, Canada.

Jula K Inrig (JK)

Travere Therapeutics, San Diego, CA, USA.

Radko Komers (R)

Travere Therapeutics, San Diego, CA, USA.

Louis-Philippe Laurin (LP)

Division of Nephrology, Maisonneuve-Rosemont Hospital, Montreal, Quebec, Canada.

Dustin J Little (DJ)

Clinical development, Late Cardiovascular, Renal and Metabolism, AstraZeneca, Gaithersburg, Maryland, USA.

Patrick H Nachman (PH)

University of Minnesota, Minneapolis, MN, USA.

Kimberly A Smith (KA)

Center for Drug Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, MD, USA.

Liron Walsh (L)

Goldfinch Bio, Boston, MA, USA.

Keisha L Gibson (KL)

University of North Carolina Kidney Center, Chapel Hill, NC, USA.

Classifications MeSH