Renal Response Criteria for Clinical Trials in Amyloid Light Chain Amyloidosis.
AL amyloidosis
clinical trial
estimated glomerular filtration rate
proteinuria
rare diseases
renal end points
Journal
Kidney international reports
ISSN: 2468-0249
Titre abrégé: Kidney Int Rep
Pays: United States
ID NLM: 101684752
Informations de publication
Date de publication:
Jul 2024
Jul 2024
Historique:
received:
26
02
2024
accepted:
25
03
2024
medline:
31
7
2024
pubmed:
31
7
2024
entrez:
31
7
2024
Statut:
epublish
Résumé
Immunoglobin light chain (AL) amyloidosis is a rare disease characterized by organ deposition of amyloid fibrils, most commonly in the heart and kidney. Disease heterogeneity necessitates organ-specific assessment to determine prognosis and response or progression. To facilitate development of new therapies, the Amyloidosis Forum (a public-private partnership between the US Food and Drug Administration and the nonprofit Amyloidosis Research Consortium) held a series of meetings and formed multiple working groups to identify clinical trial end points and analytic strategies. This report summarizes the recommendations of Renal Working Group. Estimated glomerular filtration rate (eGFR) and proteinuria were selected to evaluate eligibility, response, and/or progression in the context of investigational clinical trials for patients with AL amyloidosis. Accurate response assessments at the earliest possible time point were emphasized. The context of use, specific patient population, and the investigational therapeutic mechanism should ultimately drive selection of appropriate end points to evaluate renal response/progression in AL amyloidosis clinical trials.
Identifiants
pubmed: 39081759
doi: 10.1016/j.ekir.2024.03.033
pii: S2468-0249(24)01620-6
pmc: PMC11284377
doi:
Types de publication
Journal Article
Review
Langues
eng
Pagination
1986-1994Investigateurs
Yolanda Barbachano
(Y)
Krishna Prasad
(K)
Kimberly Smith
(K)
Informations de copyright
© 2024 International Society of Nephrology. Published by Elsevier Inc.