AZP2006 in Progressive Supranuclear Palsy: Outcomes from a Phase 2a Multicenter, Randomized Trial, and Open-Label Extension on Safety, Biomarkers, and Disease Progression.
IF 7.6
1区 医学
Q1 CLINICAL NEUROLOGY
Jean-Christophe Corvol,Mickael Alexandre Obadia,Caroline Moreau,Louise-Laure Mariani,Jean-Philippe Brandel,David Devos,Sara Sambin,Nicolas Carrière,Günter Höglinger,Marie Lebouteux,Graziella Mangone,Noelle Callizot,Aurélien Blondel,Olivier Defert,Cecilia Estrella,Artin Karapet,Philippe Verwaerde,Luc Defebvre
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Abstract
OBJECTIVES
The aim was to evaluate the safety, tolerability, pharmacokinetics, and potential clinical efficacy of AZP2006, an oral pleiotropic drug modulating progranulin levels, in patients with progressive supranuclear palsy (PSP), a rare tauopathy.
METHODS
A randomized, double-blind, placebo-controlled, parallel-group trial was conducted at three sites in France. Eligible participants (age 40-80 years, diagnosed with probable or possible PSP) were randomized to receive AZP2006 (60 mg once per day [QD] or 80/50 mg QD [80 mg for 10 days followed by 50 mg]) or placebo for 12 weeks. Assessments included safety, pharmacokinetics (plasma and whole blood), pharmacodynamics (cerebrospinal fluid and plasma biomarkers), and exploratory clinical efficacy (PSP rating scale, clinical global impression, and activities of daily living). Approximately 2 years post-trial, an open-label extension (OLE) enrolled 15 patients who received active treatment (AZP2006) for 6 months.
RESULTS
Forty-one patients were screened, 36 randomized, and 34 completed the study. AZP2006 demonstrated acceptable tolerability and safety with no treatment-related serious adverse events. Pharmacokinetic analysis confirmed rapid absorption, a long half-life (60 mg: 764.3 hours; 80/50 mg: 684.7 hours), and steady-state by day 45 (60 mg) and day 28 (80/50 mg). Biomarker analyses indicated blood-brain barrier crossing, target engagement, and stabilized progranulin levels. Trends in efficacy favored slower disease progression in AZP2006 groups. The OLE demonstrated a slowed progression of the disease and revealed no notable safety concerns.
CONCLUSIONS
AZP2006 was well-tolerated and demonstrated favorable trends in biomarker and clinical outcomes. These preliminary signals support further investigation to determine whether a meaningful clinical benefit can be achieved in PSP with AZP2006. © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
AZP2006治疗进行性核上性麻痹:来自多中心、随机试验的结果,以及安全性、生物标志物和疾病进展的开放标签扩展。
目的:评价AZP2006治疗进行性核上性麻痹(PSP)患者的安全性、耐受性、药代动力学和潜在临床疗效。AZP2006是一种口服多效性药物,可调节颗粒前蛋白水平。方法在法国三个地点进行随机、双盲、安慰剂对照、平行组试验。符合条件的参与者(年龄40-80岁,诊断为可能或可能的PSP)随机接受AZP2006(60毫克,每天一次[QD]或80/50毫克QD[80毫克,10天,随后50毫克])或安慰剂,为期12周。评估包括安全性、药代动力学(血浆和全血)、药效学(脑脊液和血浆生物标志物)和探索性临床疗效(PSP评分量表、临床总体印象和日常生活活动)。大约2年后,一项开放标签延长(OLE)研究纳入了15名患者,他们接受了6个月的积极治疗(AZP2006)。结果筛选41例患者,随机36例,完成研究34例。AZP2006表现出可接受的耐受性和安全性,无治疗相关的严重不良事件。药代动力学分析证实吸收迅速,半衰期长(60 mg: 764.3小时;80/50 mg: 684.7小时),在第45天(60 mg)和第28天(80/50 mg)达到稳定状态。生物标志物分析表明血脑屏障跨越,靶标结合和稳定的颗粒蛋白前水平。AZP2006组的疗效趋势倾向于减缓疾病进展。OLE显示疾病进展缓慢,未发现明显的安全性问题。结论sazp2006耐受性良好,在生物标志物和临床结果方面表现出良好的趋势。这些初步信号支持进一步的研究,以确定AZP2006是否能在PSP中获得有意义的临床益处。©2025作者。Wiley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》。
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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.