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皮下注射依氟鸟氨酸 PH20 治疗全身性重症肌无力:一项 3 期随机非劣效性研究(ADAPT-SC)和长期开放标签扩展研究(ADAPT-SC+)的中期分析。

Subcutaneous efgartigimod PH20 in generalized myasthenia gravis: A phase 3 randomized noninferiority study (ADAPT-SC) and interim analyses of a long-term open-label extension study (ADAPT-SC+).

机构信息

Department of Neurology, The University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

Department of Neurology, University of South Florida Morsani College of Medicine, Tampa, FL, USA.

出版信息

Neurotherapeutics. 2024 Sep;21(5):e00378. doi: 10.1016/j.neurot.2024.e00378. Epub 2024 Sep 2.

Abstract

ADAPT-SC (NCT04735432) was designed to evaluate noninferiority of subcutaneous (SC) efgartigimod PH20 to intravenous (IV) efgartigimod in participants with generalized myasthenia gravis (gMG). ADAPT-SC+ (NCT04818671) is an open-label extension study designed to assess long-term safety, tolerability, and efficacy of efgartigimod PH20 SC. Adult participants in ADAPT-SC were randomly assigned to receive a treatment cycle of 4 once-weekly administrations of efgartigimod PH20 SC 1000 ​mg or efgartigimod IV 10 ​mg/kg, followed by 7 weeks of follow-up. Primary endpoint was percentage change from baseline in total immunoglobulin G (IgG) level at week 4 (1 week after the fourth administration). Secondary efficacy endpoints assessed number and percentage of Myasthenia Gravis Activities of Daily Living (MG-ADL) and Quantitative Myasthenia Gravis (QMG) responders and mean change from baseline in total score for each measure. The primary endpoint was met, demonstrating noninferiority in total IgG reduction between efgartigimod PH20 SC 1000 ​mg and efgartigimod IV 10 ​mg/kg. Clinically meaningful improvements were seen as early as 1 week following the first administration in both treatment arms, with maximal improvements at week 4. Continued treatment cycles of efgartigimod PH20 SC in ADAPT-SC+ have demonstrated long-term safety and consistent improvements in MG-ADL total score. Findings from ADAPT-SC and ADAPT-SC+ demonstrate similar safety and efficacy as observed in the placebo-controlled ADAPT study. Collectively, these findings support noninferiority between efgartigimod PH20 SC 1000 ​mg and efgartigimod IV 10 ​mg/kg, as well as long-term safety, tolerability, and efficacy of efgartigimod PH20 SC for treatment of a broad population of patients with gMG.

摘要

ADAPT-SC(NCT04735432)旨在评估皮下(SC)依古比替单抗 PH20 相对于静脉内(IV)依古比替单抗在全身型重症肌无力(gMG)患者中的非劣效性。ADAPT-SC+(NCT04818671)是一项开放标签扩展研究,旨在评估依古比替单抗 PH20 SC 的长期安全性、耐受性和疗效。ADAPT-SC 中的成年参与者被随机分配接受 4 个治疗周期的 4 次每周一次皮下给予依古比替单抗 PH20 SC 1000mg 或依古比替单抗 IV 10mg/kg,随后进行 7 周随访。主要终点是第 4 周(第 4 次给药后 1 周)从基线时总免疫球蛋白 G(IgG)水平的变化百分比。次要疗效终点评估肌无力日常生活活动量表(MG-ADL)和定量重症肌无力(QMG)应答者的数量和百分比,以及每种措施的总评分从基线的平均变化。主要终点达到,证明了依古比替单抗 PH20 SC 1000mg 和依古比替单抗 IV 10mg/kg 之间总 IgG 降低的非劣效性。在两个治疗组中,早在第一次给药后 1 周就观察到了有临床意义的改善,在第 4 周时达到最大改善。ADAPT-SC+中依古比替单抗 PH20 SC 的连续治疗周期已证明长期安全性和 MG-ADL 总评分的持续改善。ADAPT-SC 和 ADAPT-SC+的研究结果与安慰剂对照的 ADAPT 研究观察到的安全性和疗效相似。总的来说,这些发现支持依古比替单抗 PH20 SC 1000mg 与依古比替单抗 IV 10mg/kg 之间的非劣效性,以及依古比替单抗 PH20 SC 治疗广泛人群的全身型重症肌无力患者的长期安全性、耐受性和疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a2f/11579873/538d098e8631/gr1.jpg

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