MN-166 (ibudilast) in amyotrophic lateral sclerosis in a Phase IIb/III study: COMBAT-ALS study design.

IF 2.3 Q3 CLINICAL NEUROLOGY
Neurodegenerative disease management Pub Date : 2021-12-01 Epub Date: 2021-11-24 DOI:10.2217/nmt-2021-0042
Björn Oskarsson, Nicholas Maragakis, Richard S Bedlack, Namita Goyal, Jenny A Meyer, Angela Genge, Cynthia Bodkin, Samuel Maiser, Nathan Staff, Lorne Zinman, Nicholas Olney, John Turnbull, Benjamin Rix Brooks, Emelia Klonowski, Malath Makhay, Seiichi Yasui, Kazuko Matsuda
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引用次数: 13

Abstract

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease with motor neuron loss as a defining feature. Despite significant effort, therapeutic breakthroughs have been modest. MN-166 (ibudilast) has demonstrated neuroprotective action by various mechanisms: inhibition of proinflammatory cytokines and macrophage migration inhibitory factor, phosphodiesterase inhibition, and attenuation of glial cell activation in models of ALS. Early-phase studies suggest that MN-166 may improve survival outcomes and slow disease progression in patients with ALS. This article describes the rationale and design of COMBAT-ALS, an ongoing randomized, double-blind, placebo-controlled, multicenter Phase IIb/III study in ALS. This study is designed to evaluate the pharmacokinetics, safety and tolerability and assess the efficacy of MN-166 on function, muscle strength, quality of life and survival in ALS.

MN-166(布司特)在肌萎缩性侧索硬化症的IIb/III期研究:COMBAT-ALS研究设计。
肌萎缩性侧索硬化症(ALS)是一种以运动神经元丧失为特征的神经退行性疾病。尽管付出了巨大的努力,但治疗方面的突破并不多。MN-166(布地司特)通过多种机制显示出神经保护作用:抑制促炎细胞因子和巨噬细胞迁移抑制因子,抑制磷酸二酯酶,减弱ALS模型中的胶质细胞活化。早期研究表明MN-166可能改善ALS患者的生存结果并减缓疾病进展。本文描述了COMBAT-ALS的基本原理和设计,这是一项正在进行的针对ALS的随机、双盲、安慰剂对照、多中心IIb/III期研究。本研究旨在评估MN-166的药代动力学、安全性和耐受性,并评估MN-166对ALS患者功能、肌力、生活质量和生存的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.30
自引率
0.00%
发文量
35
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