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转化神经疾病药物研发:多疾病领域研讨会论文集

Transforming Drug Development for Neurological Disorders: Proceedings from a Multidisease Area Workshop.

机构信息

Critical Path Institute, Tucson, AZ, USA.

出版信息

Neurotherapeutics. 2023 Oct;20(6):1682-1691. doi: 10.1007/s13311-023-01440-x. Epub 2023 Oct 12.

Abstract

Neurological disorders represent some of the most challenging therapeutic areas for successful drug approvals. The escalating global burden of death and disability for such diseases represents a significant worldwide public health challenge, and the rate of failure of new therapies for chronic progressive disorders of the nervous system is higher relative to other non-neurological conditions. However, progress is emerging rapidly in advancing the drug development landscape in both rare and common neurodegenerative diseases. In October 2022, the Critical Path Institute (C-Path) and the US Food and Drug Administration (FDA) organized a Neuroscience Annual Workshop convening representatives from the drug development industry, academia, the patient community, government agencies, and regulatory agencies regarding the future development of tools and therapies for neurological disorders. This workshop focused on five chronic progressive diseases: Alzheimer's disease, Parkinson's disease, Huntington's disease, Duchenne muscular dystrophy, and inherited ataxias. This special conference report reviews the key points discussed during the three-day dynamic workshop, including shared learnings, and recommendations that promise to catalyze future advancement of novel therapies and drug development tools.

摘要

神经系统疾病是药物成功获批面临的最具挑战性的治疗领域之一。这些疾病导致的全球死亡和残疾负担不断加重,是全球公共卫生面临的重大挑战,而且相对于其他非神经疾病,新型疗法治疗慢性进行性神经系统疾病的失败率更高。然而,在推进罕见和常见神经退行性疾病药物研发方面,目前正在迅速取得进展。2022 年 10 月,关键路径研究所(C-Path)和美国食品药品监督管理局(FDA)组织了一次神经科学年度研讨会,召集了来自药物研发行业、学术界、患者群体、政府机构和监管机构的代表,共同探讨神经疾病治疗工具和疗法的未来发展。本次研讨会聚焦五种慢性进行性疾病:阿尔茨海默病、帕金森病、亨廷顿病、杜氏肌营养不良症和遗传性共济失调。本专题会议报告回顾了为期三天的动态研讨会期间讨论的要点,包括经验教训和建议,有望促进新型疗法和药物研发工具的未来发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f16/10684834/09c3c28a7ce8/13311_2023_1440_Fig1_HTML.jpg

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