Limb-Girdle Muscular Dystrophy Scientific Workshop: A Multistakeholder Discussion Focused on Charting the Path Forward for Drug Development.

IF 3.2 Q3 CLINICAL NEUROLOGY
Neurology. Clinical practice Pub Date : 2025-10-01 Epub Date: 2025-07-30 DOI:10.1212/CPJ.0000000000200496
Matthew P Wicklund, Lindsay N Alfano, Nicholas E Johnson, Peter B Kang, Peter Marks, Katherine D Mathews, Jerry R Mendell, Louise Rodino-Klapac, Douglas Sproule, Nicole Verdun, Kathryn Bryant
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引用次数: 0

Abstract

Limb-girdle muscular dystrophy (LGMD) refers to a group of muscular dystrophies that generally result in weakness and loss of limb-girdle muscles, leading to severe disability and early mortality due to cardiac and respiratory complications. Heterogeneity across and within individual LGMD subtypes in addition to variability in progression rates presents significant challenges to traditional drug development approaches for these diseases. In an effort to discuss these challenges, as well as opportunities in support of advancing drug development for LGMD, on February 8, 2024, The Speak Foundation assembled a multistakeholder group consisting of academic medical experts, patients and caregivers, patient advocacy organizations, senior leaders from the US Food and Drug Administration, and commercial drug developers. This review will provide an overview of the broad range of topics discussed at the workshop, including LGMD pathophysiology, natural history studies, clinical outcomes, patient-focused drug development, surrogate end points, the Accelerated Approval pathway, and future directions for LGMD drug development.

四肢带状肌肉萎缩症科学研讨会:多利益相关者讨论的重点是绘制药物开发的前进道路。
肢带肌营养不良症(LGMD)是指一组肌肉营养不良症,通常导致肢带肌无力和丧失,导致心脏和呼吸系统并发症,导致严重残疾和早期死亡。不同LGMD亚型之间和内部的异质性以及进展率的可变性对这些疾病的传统药物开发方法提出了重大挑战。为了讨论这些挑战,以及支持推进LGMD药物开发的机遇,Speak基金会于2024年2月8日召集了一个由学术医学专家、患者和护理人员、患者倡导组织、美国食品和药物管理局的高级领导人和商业药物开发商组成的多方利益相关者小组。这篇综述将提供研讨会上讨论的广泛主题的概述,包括LGMD的病理生理学、自然史研究、临床结果、以患者为中心的药物开发、替代终点、加速审批途径以及LGMD药物开发的未来方向。
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来源期刊
Neurology. Clinical practice
Neurology. Clinical practice CLINICAL NEUROLOGY-
CiteScore
4.00
自引率
0.00%
发文量
77
期刊介绍: Neurology® Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. The journal publishes original articles in all areas of neurogenetics including rare and common genetic variations, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease genes, and genetic variations with a putative link to diseases. Articles include studies reporting on genetic disease risk, pharmacogenomics, and results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology® Genetics, but studies using model systems for treatment trials, including well-powered studies reporting negative results, are welcome.
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