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ABP 654,一种乌司奴单抗生物类似药候选药物的药代动力学相似性:健康受试者中一项随机、双盲研究的结果。

Pharmacokinetic Similarity of ABP 654, an Ustekinumab Biosimilar Candidate: Results from a Randomized, Double-blind Study in Healthy Subjects.

机构信息

Amgen Inc., Thousand Oaks, CA, USA.

出版信息

Clin Pharmacol Drug Dev. 2023 Sep;12(9):863-873. doi: 10.1002/cpdd.1301. Epub 2023 Jul 7.

DOI:10.1002/cpdd.1301
PMID:37415567
Abstract

ABP 654 is a proposed biosimilar to ustekinumab reference product (RP) which works through antagonism of interleukin-12 and interleukin-23. Ustekinumab RP is used for the treatment of chronic inflammatory conditions, including some forms of plaque psoriasis, psoriatic arthritis, Crohn's disease, and ulcerative colitis. A randomized, double-blinded, single-dose, 3-arm, parallel-group study was conducted to assess the pharmacokinetic (PK) similarity of ABP 654 with ustekinumab RP sourced from the United States (US) and the European Union (EU); the PK similarity of ustekinumab US versus ustekinumab EU; and the comparative safety, tolerability, and immunogenicity of all 3 products. A total of 238 healthy subjects were randomized 1:1:1 and stratified by gender and ethnicity (Japanese versus non-Japanese) to receive a single 90 mg subcutaneous injection of ABP 654 or ustekinumab US or ustekinumab EU. PK similarity was established based on 90% confidence intervals (CIs) for the primary endpoints of area under the concentration-time curve from time 0 extrapolated to infinity (AUC ) and maximum observed serum concentration (C ) being contained within the prespecified margin of 0.8-1.25. No clinically meaningful differences in immunogenicity were found among the 3 products. Adverse events were similar between treatment groups and consistent with the safety profile of ustekinumab RP. Results indicate that ABP 654, ustekinumab US and ustekinumab EU share similar PK and safety profiles.

摘要

ABP 654 是一种乌司奴单抗生物类似药,通过拮抗白细胞介素-12 和白细胞介素-23 起作用。乌司奴单抗 RP 用于治疗慢性炎症性疾病,包括某些形式的斑块型银屑病、银屑病关节炎、克罗恩病和溃疡性结肠炎。一项随机、双盲、单次、三臂、平行组研究旨在评估 ABP 654 与源自美国(US)和欧盟(EU)的乌司奴单抗 RP 的药代动力学(PK)相似性;乌司奴单抗 US 与乌司奴单抗 EU 的 PK 相似性;以及所有 3 种产品的安全性、耐受性和免疫原性的比较。共有 238 名健康受试者按 1:1:1 的比例随机分组,并按性别和种族(日本与非日本)分层,接受单次皮下注射 90mg ABP 654 或乌司奴单抗 US 或乌司奴单抗 EU。PK 相似性基于主要终点的 90%置信区间(CI)来建立,主要终点包括从时间 0 外推至无穷大的浓度-时间曲线下面积(AUC )和最大观察到的血清浓度(C ),这些终点均包含在 0.8-1.25 的预定范围内。在 3 种产品之间未发现免疫原性有临床意义的差异。治疗组之间的不良事件相似,与乌司奴单抗 RP 的安全性特征一致。结果表明,ABP 654、乌司奴单抗 US 和乌司奴单抗 EU 具有相似的 PK 和安全性特征。

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