QL0902, a proposed etanercept biosimilar: pharmacokinetic and immunogenicity profile to its reference product in healthy Chinese male subjects

被引:3
|
作者
Zeng, Yun [1 ]
Huang, Jie [1 ,2 ]
Cui, Chang [1 ]
Yang, Shuang [1 ]
Zhang, Ze-Yu [1 ]
Ali, Saqib [1 ]
Huang, Zhi-Jun [1 ,3 ]
Yang, Guo-Ping [1 ,2 ,3 ]
机构
[1] Cent South Univ, Xiangya Hosp 3, Ctr Clin Pharmacol, 138 TongZiPo Rd, Changsha 410013, Hunan, Peoples R China
[2] Cent South Univ, Res Ctr Drug Clin Evaluat, Changsha, Hunan, Peoples R China
[3] Cent South Univ, Xiangya Hosp 3, Dept Pharm, Changsha, Hunan, Peoples R China
基金
对外科技合作项目(国际科技项目); 中国国家自然科学基金;
关键词
Biosimilars; etanercept; pharmacokinetic; phase I; ARTHRITIS;
D O I
10.1080/14712598.2020.1745182
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Objectives: To study the pharmacokinetics, safety and immunogenicity of Recombinant Human Tumor Necrosis Factor-alpha Receptor II: IgG Fc Fusion Protein for Injection (QL0902) and evaluate the pharmacokinetic similarity between QL0902 and reference Etanercept in healthy male subjects. Methods: A randomized, double-blinded, single-dose, two-period, two-sequence and crossover study was conducted in healthy males. Sixty-eight subjects were randomized at 1:1 ratio to receive a single 50-mg subcutaneous injection of QL0902 or reference Etanercept. The statistical analysis was conducted by SAS Enterprise Guide statistical software. Results: The main pharmacokinetic parameters of QL0902 were as follows: AUC(0-infinity) was 461861.60 +/- 126861.42 (h*ng/mL), AUC(0-t) was 453304.68 +/- 124424.94 (h*ng/mL), C-max was (2634.03 +/- 833.82)ng/mL; The main pharmacokinetic parameters of reference Etanercept were as follows: AUC(0-infinity) was 537977.72 +/- 153295.70 (h*ng/mL), AUC(0-t) was 528817.19 +/- 150910.05 (h*ng/mL), C-max was (2874.21 +/- 822.31) ng/mL. Conclusions: After a single subcutaneous injection of QL0902 and reference Etanercept, the 90% confidence intervals of the ratios of AUC(0-infinity), AUC(0-t), C-max of healthy subjects were respectively 82.76% to 89.15%, 82.66% to 89.00%, 87.30% to 93.95%, which were between 80.00% and 125.00%. It indicts that their pharmacokinetic characteristics were similar. No serious adverse events occurred and the immunogenicity of QL0902 was lower.
引用
收藏
页码:105 / 110
页数:6
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