纳他珠单抗治疗后的克拉利宾片(CLADRINA)--原理与设计。

IF 4.7 2区 医学 Q1 CLINICAL NEUROLOGY Therapeutic Advances in Neurological Disorders Pub Date : 2024-04-04 eCollection Date: 2024-01-01 DOI:10.1177/17562864241233858
Peter V Sguigna, Rehana Z Hussain, Annette Okai, Kyle M Blackburn, Lauren Tardo, Mariam Madinawala, Julie Korich, Lori A Lebson, Jeffrey Kaplan, Amber Salter, Navid Manouchehri, Olaf Stuve
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引用次数: 0

摘要

背景:获准用于多发性硬化症(MS)的单个疾病调节疗法疗效有限,而且可能会产生严重的副作用,尤其是在长期用药的情况下。序贯联合疗法是一种可行的替代方法。纳他珠单抗是一种单克隆治疗抗体,可减少白细胞进入中枢神经系统,但停药后发生进行性多灶性白质脑病和疾病再激活的风险增加。克拉利宾片作为一种合成的腺苷类似物,会破坏 DNA 的合成和修复,从而减少淋巴细胞的数量。从纳他珠单抗过渡到克拉利宾的过程中,前瞻性、严格的安全性和有效性数据的产生是一项尚未满足的临床需求:目的:测试复发性多发性硬化症患者从纳他珠单抗过渡到克拉利宾片治疗的可行性:设计:纳他珠单抗治疗后服用克拉地宾片(CLADRINA)是一项开放标签、单臂、多中心、IV期合作研究,该研究将就复发性多发性硬化症患者从纳他珠单抗过渡到克拉地宾片的安全性、有效性和免疫学影响提出假设:将从三个不同地点招募参与者。主要终点是淋巴细胞和骨髓细胞亚群以及血液神经丝光水平与基线相比的绝对值和百分比变化。次要终点是 12 个月和 24 个月试验期间的年复发率。探索性终点包括扩展残疾状况量表和磁共振成像结果:CLADRINA试验将产生有关从纳他珠单抗向克拉德里滨过渡的安全性、有效性和免疫学影响的数据。随着对多发性硬化症免疫学知识了解的不断深入,我们需要深入了解疾病修饰疗法的过渡策略。
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Cladribine tablets after treatment with natalizumab (CLADRINA) - rationale and design.

Background: Individual disease modifying therapies approved for multiple sclerosis (MS) have limited effectiveness and potentially serious side effects, especially when administered over long periods. Sequential combination therapy is a plausible alternative approach. Natalizumab is a monoclonal therapeutic antibody that reduces leukocyte access to the central nervous system that is associated with an increased risk of progressive multifocal leukoencephalopathy and disease reactivation after its discontinuation. Cladribine tablets act as a synthetic adenosine analog, disrupting DNA synthesis and repair, thereby reducing the number of lymphocytes. The generation of prospective, rigorous safety, and efficacy data in transitioning from natalizumab to cladribine is an unmet clinical need.

Objectives: To test the feasibility of transitioning patients with relapsing forms of MS natalizumab to cladribine tablets.

Design: Cladribine tablets after treatment with natalizumab (CLADRINA) is an open-label, single-arm, multicenter, collaborative phase IV, research study that will generate hypothesis regarding the safety, efficacy, and immunological impact of transition from natalizumab to cladribine tablets in patients with relapsing forms of MS.

Methods and analysis: Participants will be recruited from three different sites. The primary endpoint is the absolute and percent change from baseline of lymphocytes and myeloid cell subsets, as well as blood neurofilament light levels. The secondary endpoint is the annualized relapse rate over the 12- and 24-month trial periods. Exploratory endpoints include the expanded disability status scale, and magnetic resonance imaging outcomes.

Discussion: The CLADRINA trial will generate data regarding the safety, efficacy, and immunological impact of the transition from natalizumab to cladribine. As the pace of immunological knowledge of MS continues, insight into disease modifying therapy transition strategies is needed.

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来源期刊
CiteScore
8.30
自引率
1.70%
发文量
62
审稿时长
15 weeks
期刊介绍: Therapeutic Advances in Neurological Disorders is a peer-reviewed, open access journal delivering the highest quality articles, reviews, and scholarly comment on pioneering efforts and innovative studies across all areas of neurology. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in neurology, providing a forum in print and online for publishing the highest quality articles in this area.
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