226P Phase 3, randomized, global study assessing efficacy and safety of del-desiran for the treatment of myotonic dystrophy type 1: HARBOR trial design

IF 2.7 4区 医学 Q2 CLINICAL NEUROLOGY Neuromuscular Disorders Pub Date : 2024-10-01 DOI:10.1016/j.nmd.2024.07.077
M. Fowler , N. Johnson , C. Thornton , J. Day , V. Sansone , B. McEvoy , L. Tai , B. Knisely , T. Brandt , K. Gallagher , S. Hughes , E. Ackermann
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Abstract

Myotonic dystrophy type 1 (DM1) is a rare, dominantly inherited, progressive neuromuscular disease caused by a toxic gain-of-function mutation in the DM1 protein kinase (DMPK) gene. DM1 is primarily characterized by myotonia along with progressive muscular weakness and wasting, leading to deficits in hand function, immobility, respiratory insufficiency, dysarthria, and dysphagia. Hand function impairment is caused by both myotonia and hand weakness leading to negative impact on quality of life. Delpacibart etedesiran (del-desiran, formerly AOC 1001) is an antibody-oligonucleotide conjugate (AOC™) comprised of a DMPK siRNA conjugated to a humanized antibody targeting transferrin receptor 1 (TfR1) for delivery of siRNA to muscle cells to mediate DMPK mRNA degradation addressing the underlying cause of DM1. Long-term safety and tolerability data from the Phase 1/2 MARINA® and MARINA-OLE™ clinical trials demonstrated that del-desiran is well tolerated in patients with DM1 and demonstrated efficacy compared to placebo and natural history for multiple functional endpoints. This phase 3, randomized, double-blind, placebo-controlled, 54-week study will be conducted across ∼40 global sites. This study will enroll participants aged 16+ years with a clinical and genetic diagnosis of DM1 (DMPK CTG repeat ≥100). Participants will be randomized 1:1 to receive either 4 mg/kg del-desiran or placebo administered intravenously every 8 weeks. The first dose of del-desiran will be 2 mg/kg. Primary analysis will take place at Week 30, with the duration of the placebo-controlled study being 54 weeks. Eligible participants will have the option to enroll in an open-label extension trial. The primary objective is to evaluate the efficacy of del-desiran on hand opening time to observe changes in myotonia and hand function. Key secondary objectives are to evaluate the efficacy of del-desiran on muscle strength and activities of daily living.
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226P 评估德尔-地西兰治疗 1 型肌营养不良症疗效和安全性的 3 期随机全球研究:HARBOR 试验设计
肌营养不良症 1 型(DM1)是一种罕见的显性遗传进行性神经肌肉疾病,由 DM1 蛋白激酶(DMPK)基因的毒性功能增益突变引起。DM1 的主要特征是肌张力障碍以及进行性肌肉无力和萎缩,从而导致手部功能障碍、行动不便、呼吸功能不全、构音障碍和吞咽困难。肌张力障碍和手部无力都会导致手部功能障碍,从而对生活质量造成负面影响。Delpacibart etedesiran(del-desiran,原 AOC 1001)是一种抗体-寡核苷酸共轭物(AOC™),由 DMPK siRNA 与靶向转铁蛋白受体 1(TfR1)的人源化抗体共轭组成,用于向肌肉细胞递送 siRNA,以介导 DMPK mRNA 降解,从而解决 DM1 的根本原因。1/2期MARINA®和MARINA-OLE™临床试验的长期安全性和耐受性数据表明,Del-desiran在DM1患者中耐受性良好,在多个功能终点方面与安慰剂和自然病史相比具有疗效。这项为期 54 周的 3 期随机、双盲、安慰剂对照研究将在全球 40 个地点进行。这项研究将招募年龄在16岁以上、临床和基因诊断为DM1(DMPK CTG重复≥100)的参与者。参与者将按1:1的比例随机接受每8周静脉注射4毫克/千克del-desiran或安慰剂。del-desiran的首次剂量为2毫克/千克。主要分析将在第30周进行,安慰剂对照研究的持续时间为54周。符合条件的参与者可选择参加开放标签延长试验。研究的主要目的是评估德尔地西兰对手部张开时间的疗效,观察肌张力和手部功能的变化。主要次要目标是评估del-desiran对肌力和日常生活活动的疗效。
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来源期刊
Neuromuscular Disorders
Neuromuscular Disorders 医学-临床神经学
CiteScore
4.60
自引率
3.60%
发文量
543
审稿时长
53 days
期刊介绍: This international, multidisciplinary journal covers all aspects of neuromuscular disorders in childhood and adult life (including the muscular dystrophies, spinal muscular atrophies, hereditary neuropathies, congenital myopathies, myasthenias, myotonic syndromes, metabolic myopathies and inflammatory myopathies). The Editors welcome original articles from all areas of the field: • Clinical aspects, such as new clinical entities, case studies of interest, treatment, management and rehabilitation (including biomechanics, orthotic design and surgery). • Basic scientific studies of relevance to the clinical syndromes, including advances in the fields of molecular biology and genetics. • Studies of animal models relevant to the human diseases. The journal is aimed at a wide range of clinicians, pathologists, associated paramedical professionals and clinical and basic scientists with an interest in the study of neuromuscular disorders.
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