Clinical evaluation of ThecaFlex DRx, a novel implantable catheter-port for intrathecal nusinersen delivery in spinal muscular atrophy: Initial results from the PIERRE-IDE study.

IF 3.5 4区 医学 Q2 CLINICAL NEUROLOGY
Journal of neuromuscular diseases Pub Date : 2026-09-01 Epub Date: 2026-03-13 DOI:10.1177/22143602261432303
Ignacio Mesina-Estarrón, Michael Abruzzo, Fernando Cotrim Gomes, Melina Thaxton, Aaron Yengo-Kahn, Scellig Stone, Weston Northam, Brian Snyder, Patrick Cahill, David Bauer, Michael Muhonen
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引用次数: 0

Abstract

Background: Administration of Nusinersen requires repeated lumbar intrathecal access, posing challenges for patients with Spinal Muscular Atrophy (SMA). A purpose-built system may streamline drug delivery.

Objective: To assess the feasibility and safety of ThecaFlex DRx for intrathecal Nusinersen dosing.

Methods: We present initial results of a prospective, multicenter investigational device exemption (IDE) study. Patients with SMA who had an indication for intrathecal Nusinersen were enrolled. Primary outcomes were successful system implantation and postoperative infusion. Prespecified safety outcomes consisted of adverse events adjudicated for severity and device or procedure relatedness.

Results: Twenty-five subjects underwent device implantation. Median age at implantation was 13.8 years (IQR 10.0-18.0), and 52% were female. Subjects included individuals with SMA types I (16%), II (64%), and III (20%). Implantation was successful in all cases. At the interim data cutoff, median follow-up was 230 days (IQR 76.0-369.0) at which point 23 subjects (92%) had successfully received Nusinersen infusions. Ten patients reached one year of follow-up, and all of them maintained a functional device at this visit. Sixty adverse events occurred in 19 subjects, with 12 events (20%) adjudicated as serious adverse events that were most commonly wound-related or respiratory. At one year, the estimated probability of remaining free from device action was 86.2% (95% CI 0.73-1.00), with two devices requiring explantation due to wound dehiscence and access difficulties, respectively.

Conclusions: This interim report supports the feasibility of ThecaFlex DRx for Nusinersen administration, with long-term durability and effectiveness to be defined with longer follow-up.For more information about the PIERRE study (NCT05866419), visit: https://www.

Clinicaltrials: gov/study/NCT05866419.

caflex DRx,一种用于脊髓性肌萎缩患者鞘内注射的新型可植入导管口的临床评价:PIERRE-IDE研究的初步结果
背景:Nusinersen的给药需要反复腰椎鞘内通路,这给脊髓性肌萎缩(SMA)患者带来了挑战。专门建造的系统可以简化药物输送。目的:评价ThecaFlex DRx鞘内给药的可行性和安全性。方法:我们提出了一项前瞻性、多中心研究性器械豁免(IDE)研究的初步结果。纳入有鞘内Nusinersen指征的SMA患者。主要结果是成功的系统植入和术后输液。预先指定的安全结果包括不良事件的严重程度和设备或程序的相关性。结果:25例患者接受了器械植入。中位着床年龄13.8岁(IQR 10.0 ~ 18.0), 52%为女性。受试者包括SMA I型(16%)、II型(64%)和III型(20%)患者。所有病例均成功植入。在中期数据截止时,中位随访时间为230天(IQR 76.0-369.0),其中23例(92%)患者成功接受了Nusinersen输注。10例患者随访1年,所有患者在本次访视时均保留了功能装置。在19名受试者中发生了60起不良事件,其中12起(20%)被判定为最常见的与伤口或呼吸有关的严重不良事件。在一年时,估计不受装置作用影响的概率为86.2% (95% CI 0.73-1.00),其中两个装置分别因伤口裂开和进入困难而需要取出。结论:本中期报告支持ThecaFlex DRx用于Nusinersen给药的可行性,其长期持久性和有效性有待于更长时间的随访。有关PIERRE研究(NCT05866419)的更多信息,请访问:https://www.Clinicaltrials: gov/study/NCT05866419。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of neuromuscular diseases
Journal of neuromuscular diseases Medicine-Neurology (clinical)
CiteScore
5.10
自引率
6.10%
发文量
102
期刊介绍: The Journal of Neuromuscular Diseases aims to facilitate progress in understanding the molecular genetics/correlates, pathogenesis, pharmacology, diagnosis and treatment of acquired and genetic neuromuscular diseases (including muscular dystrophy, myasthenia gravis, spinal muscular atrophy, neuropathies, myopathies, myotonias and myositis). The journal publishes research reports, reviews, short communications, letters-to-the-editor, and will consider research that has negative findings. The journal is dedicated to providing an open forum for original research in basic science, translational and clinical research that will improve our fundamental understanding and lead to effective treatments of neuromuscular diseases.
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