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Disease-modifying therapies for Parkinson disease: lessons from multiple sclerosis.

Authors :
Kalia LV
Asis A
Arbour N
Bar-Or A
Bove R
Di Luca DG
Fon EA
Fox S
Gan-Or Z
Gommerman JL
Kang UJ
Klawiter EC
Koch M
Kolind S
Lang AE
Lee KK
Lincoln MR
MacDonald PA
McKeown MJ
Mestre TA
Miron VE
Ontaneda D
Rousseaux MWC
Schlossmacher MG
Schneider R
Stoessl AJ
Oh J
Source :
Nature reviews. Neurology [Nat Rev Neurol] 2024 Oct 07. Date of Electronic Publication: 2024 Oct 07.
Publication Year :
2024
Publisher :
Ahead of Print

Abstract

The development of disease-modifying therapies (DMTs) for neurological disorders is an important goal in modern neurology, and the associated challenges are similar in many chronic neurological conditions. Major advances have been made in the multiple sclerosis (MS) field, with a range of DMTs being approved for relapsing MS and the introduction of the first DMTs for progressive MS. By contrast, people with Parkinson disease (PD) still lack such treatment options, relying instead on decades-old therapeutic approaches that provide only symptomatic relief. To address this unmet need, an in-person symposium was held in Toronto, Canada, in November 2022 for international researchers and experts in MS and PD to discuss strategies for advancing DMT development. In this Roadmap article, we highlight discussions from the symposium, which focused on therapeutic targets and preclinical models, disease spectra and subclassifications, and clinical trial design and outcome measures. From these discussions, we propose areas for novel or deeper exploration in PD using lessons learned from therapeutic development in MS. In addition, we identify challenges common to the PD and MS fields that need to be addressed to further advance the discovery and development of effective DMTs.<br /> (© 2024. Springer Nature Limited.)

Details

Language :
English
ISSN :
1759-4766
Database :
MEDLINE
Journal :
Nature reviews. Neurology
Publication Type :
Academic Journal
Accession number :
39375563
Full Text :
https://doi.org/10.1038/s41582-024-01023-0