Anti-Neuroinflammatory and Anti-Inflammatory Effects of the NLRP3 Inhibitor NT-0796 in Subjects with Parkinson's Disease.

IF 7.6 1区 医学 Q1 CLINICAL NEUROLOGY
Nicholas Clarke,Peter Thornton,Valérie Reader,Nicola Lindsay,Zsofia Digby,Bianca Mullen,Michelle Gorman,Eric Jacobson,Grant Langdon,Hilary Johnstone,Alistair Wheeler,Alan P Watt
{"title":"Anti-Neuroinflammatory and Anti-Inflammatory Effects of the NLRP3 Inhibitor NT-0796 in Subjects with Parkinson's Disease.","authors":"Nicholas Clarke,Peter Thornton,Valérie Reader,Nicola Lindsay,Zsofia Digby,Bianca Mullen,Michelle Gorman,Eric Jacobson,Grant Langdon,Hilary Johnstone,Alistair Wheeler,Alan P Watt","doi":"10.1002/mds.30307","DOIUrl":null,"url":null,"abstract":"BACKGROUND\r\nInhibition of Nod-like receptor protein 3 (NLRP3) inflammasome within the central nervous system (CNS) is a promising therapeutic target for the treatment of Parkinson's disease (PD).\r\n\r\nOBJECTIVES\r\nThis phase 1b open-label study was conducted in elderly healthy volunteers (HV) and PD patients. The study was designed to assess safety and tolerability and to evaluate the central and systemic pharmacokinetic profile and anti-inflammatory effects of a total daily dose of 300 mg NT-0796 (oral 150 mg suspension capsule formulation every 12 h).\r\n\r\nMETHODS\r\nFour elderly HV and 10 subjects with PD received 150 mg open-label NT-0796 every 12 h for either 7 or 28 days, respectively. Blood and cerebrospinal fluid (CSF) were collected via serial sampling or lumbar punctures for pharmacokinetic and biomarker analyses. Standard safety parameters were monitored throughout.\r\n\r\nRESULTS\r\nNT-0796 was safe and well tolerated with minimal adverse events. A reduced peak-to-trough ratio along with moderately higher exposure than the solution formulation (used in the first-in-human study) was observed, along with significant CSF exposure in elderly HV and subjects with PD. NT-0796 drove reductions in systemic inflammatory markers including high-sensitivity C-reactive protein, fibrinogen, interleukin (IL)-6, and IL-18. Furthermore, reductions in neuroinflammation, including IL-1β, were indicative of NT-0796's target engagement within the central nervous system (CNS) of subjects with PD.\r\n\r\nCONCLUSIONS\r\nCNS inhibition of NLRP3 with NT-0796 reduced neuroinflammation over a sustained 28-day dosing period and demonstrates the potential for long-term dosing of NT-0796 in future studies of patients with neurodegeneration. © 2025 NodThera Limited. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.","PeriodicalId":213,"journal":{"name":"Movement Disorders","volume":"53 1","pages":""},"PeriodicalIF":7.6000,"publicationDate":"2025-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Movement Disorders","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1002/mds.30307","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

BACKGROUND Inhibition of Nod-like receptor protein 3 (NLRP3) inflammasome within the central nervous system (CNS) is a promising therapeutic target for the treatment of Parkinson's disease (PD). OBJECTIVES This phase 1b open-label study was conducted in elderly healthy volunteers (HV) and PD patients. The study was designed to assess safety and tolerability and to evaluate the central and systemic pharmacokinetic profile and anti-inflammatory effects of a total daily dose of 300 mg NT-0796 (oral 150 mg suspension capsule formulation every 12 h). METHODS Four elderly HV and 10 subjects with PD received 150 mg open-label NT-0796 every 12 h for either 7 or 28 days, respectively. Blood and cerebrospinal fluid (CSF) were collected via serial sampling or lumbar punctures for pharmacokinetic and biomarker analyses. Standard safety parameters were monitored throughout. RESULTS NT-0796 was safe and well tolerated with minimal adverse events. A reduced peak-to-trough ratio along with moderately higher exposure than the solution formulation (used in the first-in-human study) was observed, along with significant CSF exposure in elderly HV and subjects with PD. NT-0796 drove reductions in systemic inflammatory markers including high-sensitivity C-reactive protein, fibrinogen, interleukin (IL)-6, and IL-18. Furthermore, reductions in neuroinflammation, including IL-1β, were indicative of NT-0796's target engagement within the central nervous system (CNS) of subjects with PD. CONCLUSIONS CNS inhibition of NLRP3 with NT-0796 reduced neuroinflammation over a sustained 28-day dosing period and demonstrates the potential for long-term dosing of NT-0796 in future studies of patients with neurodegeneration. © 2025 NodThera Limited. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
NLRP3抑制剂NT-0796在帕金森病患者中的抗神经炎和抗炎作用
中枢神经系统(CNS)内抑制nod样受体蛋白3 (NLRP3)炎性体是治疗帕金森病(PD)的一个有希望的治疗靶点。目的:这项1b期开放标签研究在老年健康志愿者(HV)和PD患者中进行。该研究旨在评估NT-0796的安全性和耐受性,并评估每日总剂量300 mg NT-0796(每12小时口服150 mg悬浮胶囊制剂)的中枢和全身药代动力学特征和抗炎作用。方法4例老年HV患者和10例PD患者每12 h接受150 mg开放标签NT-0796治疗,疗程分别为7天和28天。通过连续取样或腰椎穿刺收集血液和脑脊液(CSF)进行药代动力学和生物标志物分析。标准安全参数全程监测。结果snt -0796安全性好,耐受性好,不良事件最少。与首次人体研究中使用的溶液配方相比,观察到峰谷比降低,暴露程度中等,老年HV和PD患者的脑脊液暴露也显著增加。NT-0796降低了全身炎症标志物,包括高敏c反应蛋白、纤维蛋白原、白细胞介素(IL)-6和IL-18。此外,神经炎症的减少,包括IL-1β,表明NT-0796在PD患者的中枢神经系统(CNS)中的靶标作用。结论:NT-0796对NLRP3的scns抑制在持续28天的给药期内减少了神经炎症,并表明NT-0796在神经退行性疾病患者的未来研究中具有长期给药的潜力。©2025 NodThera LimitedWiley期刊有限责任公司代表国际帕金森和运动障碍学会出版的《运动障碍》。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Movement Disorders
Movement Disorders 医学-临床神经学
CiteScore
13.30
自引率
8.10%
发文量
371
审稿时长
12 months
期刊介绍: Movement Disorders publishes a variety of content types including Reviews, Viewpoints, Full Length Articles, Historical Reports, Brief Reports, and Letters. The journal considers original manuscripts on topics related to the diagnosis, therapeutics, pharmacology, biochemistry, physiology, etiology, genetics, and epidemiology of movement disorders. Appropriate topics include Parkinsonism, Chorea, Tremors, Dystonia, Myoclonus, Tics, Tardive Dyskinesia, Spasticity, and Ataxia.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信