Randomized, Placebo Controlled Trial of NPT088, A Phage-Derived, Amyloid-Targeted Treatment for Alzheimer’s Disease

IF 8.5 3区 医学 Q1 CLINICAL NEUROLOGY Jpad-Journal of Prevention of Alzheimers Disease Pub Date : 2019-01-01 DOI:10.14283/jpad.2019.37
D. Michelson, M. Grundman, K. Magnuson, R. Fisher, Jonathan M. Levenson, Paul S. Aisen, K. Marek, Martha Gray, Franz Hefti
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引用次数: 9

Abstract

The engineered fusion protein NPT088 targets amyloid in vitro and in animal models of Alzheimer’s disease. Previous studies showed that NPT088 treatment reduced β-amyloid plaque and tau aggregate loads in mouse disease models. Here, we present the results from an initial clinical study of NPT088 in patients with mild to moderate Alzheimer’s disease. Patients were treated with 4 dose levels of NPT088 for 6 months to evaluate its safety and tolerability. Exploratory measurements included measurement of change in β-amyloid plaque and tau burden utilizing Positron Emission Tomography imaging as well as measures of Alzheimer’s disease symptoms. At endpoint NPT088 was generally safe and well-tolerated with the most prominent finding being infusion reactions in a minority of patients. No effect of NPT088 on brain plaques, tau aggregates or Alzheimer’s disease symptoms was observed.
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NPT088是一种噬菌体衍生的淀粉样蛋白靶向治疗阿尔茨海默病的随机安慰剂对照试验
工程融合蛋白NPT088在体外和阿尔茨海默病动物模型中靶向淀粉样蛋白。先前的研究表明,在小鼠疾病模型中,NPT088治疗降低了β-淀粉样蛋白斑块和tau聚集负荷。在这里,我们介绍了NPT088在轻度至中度阿尔茨海默病患者中的初步临床研究结果。患者接受4个剂量水平的NPT088治疗6个月,以评估其安全性和耐受性。探索性测量包括利用正电子发射断层成像测量β-淀粉样蛋白斑块和tau负荷的变化以及阿尔茨海默病症状的测量。在终点,NPT088总体上是安全且耐受性良好的,最突出的发现是在少数患者中出现输注反应。未观察到NPT088对脑斑块、tau聚集物或阿尔茨海默病症状的影响。
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来源期刊
自引率
7.80%
发文量
85
期刊介绍: The JPAD « Journal of Prevention of Alzheimer’Disease » will publish reviews, original research articles and short reports to improve our knowledge in the field of Alzheimer prevention including : neurosciences, biomarkers, imaging, epidemiology, public health, physical cognitive exercise, nutrition, risk and protective factors, drug development, trials design, and heath economic outcomes. JPAD will publish also the meeting abstracts from Clinical Trial on Alzheimer Disease (CTAD) and will be distributed both in paper and online version worldwide.
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