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ALXN1820(Tarperprumig)在健康成年人中的安全性、耐受性、药代动力学、药效学及免疫原性:一项I期研究的结果

Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Immunogenicity of ALXN1820 (Tarperprumig) in Healthy Adults: Results of a Phase I Study.

作者信息

Sandhu Avner, Shen Tong, Herrero Paz Martin, Yuan Chao-Xing, Qureshi Samirah, Jiang Xiaoyu, Sheng Ye, Gasteyger Christoph, Dai Yang

机构信息

Alexion, AstraZeneca Rare Disease, Inc., Boston, Massachusetts, USA.

出版信息

Clin Transl Sci. 2025 Apr;18(4):e70190. doi: 10.1111/cts.70190.

Abstract

Properdin is an endogenous positive regulator of the complement alternative pathway (AP). Tarperprumig (ALXN1820), a novel humanized bispecific antibody, binds properdin and albumin and is being developed to treat complement-mediated diseases. This phase I, randomized, double-blind, placebo-controlled trial assessed the safety, tolerability, pharmacokinetics (PK), pharmacodynamics, and immunogenicity of tarperprumig in healthy adult participants. In cohorts 1 to 4 and 6, single doses of tarperprumig were administered via subcutaneous (SC) injection (12.5, 50, 150, 450, and 1200 mg doses). In cohorts 8 and 9, the 150 mg dose was given via SC injection once weekly for 5 doses. In cohort 5, a single dose of 450 mg was administered via intravenous infusion. Sixty participants were randomized (3:1) to tarperprumig or placebo. There were no discontinuations due to adverse events (AEs) in participants receiving tarperprumig. There were no serious AEs, events of serious infection, or deaths. No N. meningitidis infections occurred. Most AEs were mild and not treatment related. Tarperprumig exposure resulted in linear dose proportionality among all but one cohort. Mean absolute bioavailability of tarperprumig was 94%. AP activity decreased rapidly after tarperprumig administration. Complete AP inhibition (< 1% of baseline value) was observed in all cohorts except for cohort 1 (12.5 mg SC). There was no change in complement classical or lectin pathway activity. Antidrug antibody titers were mostly low and did not impact PK. Tarperprumig was well tolerated and completely inhibited the AP in healthy adults. These results support continued investigation of tarperprumig to treat diseases involving complement activation. Trial Registration: EudraCT: 2021-002472-39/NCT04631562.

摘要

备解素是补体替代途径(AP)的内源性正调节因子。塔普普瑞米(ALXN1820)是一种新型人源化双特异性抗体,可结合备解素和白蛋白,目前正在开发用于治疗补体介导的疾病。这项I期随机、双盲、安慰剂对照试验评估了塔普普瑞米在健康成年受试者中的安全性、耐受性、药代动力学(PK)、药效学和免疫原性。在第1至4组和第6组中,通过皮下(SC)注射给予单剂量的塔普普瑞米(剂量分别为12.5、50、150、450和1200 mg)。在第8组和第9组中,每周通过SC注射给予150 mg剂量,共5剂。在第5组中,通过静脉输注给予单剂量450 mg。60名受试者被随机(3:1)分配至塔普普瑞米组或安慰剂组。接受塔普普瑞米的受试者中没有因不良事件(AE)而停药的情况。没有严重AE、严重感染事件或死亡。没有发生脑膜炎奈瑟菌感染。大多数AE为轻度,与治疗无关。除一个队列外,塔普普瑞米的暴露导致所有队列中呈线性剂量比例关系。塔普普瑞米的平均绝对生物利用度为94%。给予塔普普瑞米后,AP活性迅速下降。除第1组(12.5 mg SC)外,所有队列均观察到完全AP抑制(<基线值的1%)。补体经典途径或凝集素途径活性没有变化。抗药物抗体滴度大多较低,且不影响PK。塔普普瑞米耐受性良好,在健康成年人中完全抑制了AP。这些结果支持继续研究塔普普瑞米以治疗涉及补体激活的疾病。试验注册号:EudraCT:2021-002472-39/NCT04631562。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60d8/11936838/b8d9415610d1/CTS-18-e70190-g002.jpg

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