NM101 NE3107治疗阿尔茨海默病的III期研究:原理、设计和对神经炎症和胰岛素抵抗的治疗调节。

IF 2.3 Q3 CLINICAL NEUROLOGY Neurodegenerative disease management Pub Date : 2021-08-01 Epub Date: 2021-07-12 DOI:10.2217/nmt-2021-0022
Christopher L Reading, Clarence N Ahlem, Michael F Murphy
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引用次数: 0

摘要

最近,人们对炎症和胰岛素抵抗在神经退行性变中的作用有了更深入的认识。NE3107是一种口服小分子、血脑屏障抗炎胰岛素增敏剂,能与细胞外信号调节激酶结合,已被证明能选择性地抑制炎症驱动的ERK和NF-κB刺激的炎症介质,包括TNF-α,而不抑制其平衡功能。我们介绍了 NM101 的原理和设计,这是首个随机、多中心 III 期临床研究,目的是考察 NE3107 与安慰剂相比,在轻度至中度阿尔茨海默病老年患者中治疗 30 周的安全性和有效性。患者(316人)将按1:1的比例随机分组。共同主要终点测量认知功能(ADAS Cog12)以及功能和行为特征(ADCS CGIC)。试验注册号NCT04669028(Clinicaltrials.gov)。
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NM101 Phase III study of NE3107 in Alzheimer's disease: rationale, design and therapeutic modulation of neuroinflammation and insulin resistance.

Recently, the roles of inflammation and insulin resistance in neurodegeneration have become better appreciated. NE3107, an oral small molecule, blood-brain permeable anti-inflammatory insulin sensitizer that binds extracellular signal-regulated kinase, has been shown to selectively inhibit inflammation-driven ERK- and NF-κB-stimulated inflammatory mediators, including TNF-α, without inhibiting their homeostatic functions. We describe the rationale and design of NM101, the first randomized, multicenter Phase III clinical study to examine the safety and efficacy of 30 week treatment with NE3107 versus placebo in elderly adults with mild-to-moderate Alzheimer's disease. Patients (316) will be randomized in a 1:1 ratio. The co-primary end points measure cognitive function (ADAS Cog12), and functional and behavioral characteristics (ADCS CGIC). Trial registration number: NCT04669028 (Clinicaltrials.gov).

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