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Utility of patient subgrouping in ALS clinical trials: a World Federation of Neurology white paper

  • Jeffrey Rosenfeld*
  • , Sharon Abrahams
  • , Caroline McHutchinson
  • , Senda Ajroud-Driss
  • , Markus Weber
  • , Sabrina Paganoni
  • , Hiroshi Mitsumoto
  • , Angela Genge
  • , Julian Grosskreutz
  • , Leonard Van Den Berg
  • , Jinsy Andrews
  • , Matthew C. Kiernan
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

The heterogeneity among the amyotrophic lateral sclerosis (ALS)/MND patient population is well recognized but not well understood. Such heterogeneity may represent a significant confound in our current and prior clinical trials as certain subgroups of patients might have a selective response (or resistance) to a novel therapeutic. The basis on which to segregate the patient population is, however, unclear. The ALS/MND Committee of the World Federation of Neurology (WFN) convened a symposium to discuss various strategies that might be considered for separating (stratifying) the population to further study. The results of that conference are presented here as a white paper, reflecting current understanding of several of the various criteria that could be implemented to divide the patient population as presented and discussed at that meeting. Consideration of grouping patients based on phenotype, cognitive involvement, imaging, or electrophysiology is presented here.

Original languageEnglish
Pages (from-to)493-500
JournalAmyotrophic Lateral Sclerosis and Frontotemporal Degeneration
Volume27
Issue number5-6
Early online date8 Dec 2025
DOIs
Publication statusPublished - Aug 2026

Keywords

  • ALS heterogeneity
  • ALS subtypes
  • clinical trial design
  • stratification
  • subgrouping

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