期刊
MEDICINAL RESEARCH REVIEWS
卷 41, 期 5, 页码 2804-2822出版社
WILEY
DOI: 10.1002/med.21725
关键词
amyotrophic lateral sclerosis; clinical trials; disease mechanisms; drugs; therapeutic strategies
资金
- Russian Foundation for Basic Research [20-34-70059]
- Russian Science Foundation [18-15-00357]
- Russian Science Foundation [18-15-00357] Funding Source: Russian Science Foundation
Recent progress in understanding pathological changes in the nervous system and other body systems, such as the immune system, has revealed potential therapeutic targets for the development and progression of ALS. Many drugs have been developed to restore functionality compromised in ALS and other diseases. Current research is focused on repurposing these old drugs for the treatment of ALS patients.
Recent progress in understanding the pathological changes in the nervous system and in certain other body systems (e.g., immune system) that lead to the development and progression of amyotrophic lateral sclerosis (ALS) revealed a number of molecular and cellular processes that can potentially be used as therapeutic targets. Many of these processes are compromised not only in ALS but also in other diseases and a repertoire of drugs able to restore, at least partially, their functionality has been developed. In this review, we briefly describe current approaches to the repurposing of such old drugs for treatment of patients with ALS.
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