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Published on: May 2, 2025
Combination Disease-Modifying Therapy for Neurodegenerative Diseases Using Repurposed Drugs
Alexander Shtilbans1,2, Anthony E Lang3
1Department of Neurology, Hospital for Special Surgery, New York, NY.
Existing drugs show promise for neurodegenerative diseases (NDs) like Parkinson's and Alzheimer's. Repurposing these drugs in combination may offer a new strategy for neuroprotection.
Area of Science:
- Neuroscience
- Pharmacology
- Drug Discovery
Background:
- Neurodegenerative diseases (NDs) like Parkinson's disease (PD), Alzheimer's disease (AD), amyotrophic lateral sclerosis (ALS), and Huntington's disease (HD) represent a significant unmet medical need.
- Current therapeutic strategies for NDs are limited, necessitating novel approaches.
Purpose of the Study:
- To review the neuroprotective potential of existing drugs from various classes in preclinical models and human data for common NDs.
- To explore the concept of combinatory neuroprotective therapy using drug repurposing.
- To propose a strategy for designing ideal drug combinations to combat neurodegeneration.
Main Methods:
- Literature review of preclinical studies and published human data on drugs including chemical chaperones, GLP-1 RAs, iron chelators, and c-Abl TKIs.
- Conceptual analysis of drug repurposing for neuroprotection.
- Strategic proposal for combination therapy design.
Main Results:
- Several drug classes, including chemical chaperones, GLP-1 RAs, iron chelators, and c-Abl TKIs, demonstrate positive effects in preclinical models of NDs.
- Published human data suggest potential benefits of these repurposed drugs in individuals with PD, AD, ALS, and HD.
- Drug repurposing offers a viable strategy for developing combination therapies for NDs.
Conclusions:
- Existing drugs from diverse classes hold promise for treating neurodegenerative diseases.
- Combinatory neuroprotective therapy, leveraging drug repurposing, is a strategic approach to address the complexity of neurodegeneration.
- Designing ideal drug combinations targeting multiple pathogenic pathways is crucial for achieving clinically meaningful outcomes in NDs.
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