Phase 1 studies comparing safety, tolerability, pharmacokinetics and pharmacodynamics of HLX01(a rituximab biosimilar) to reference rituximab in Chinese patients with CD20-positive B-cell lymphoma

被引:2
作者
Yuankai Shi [1 ]
Qingyuan Zhang [2 ]
Xiaohong Han [1 ]
Yan Qin [1 ]
Xiaoyan Ke [3 ]
Hang Su [4 ]
Li Liu [5 ]
Jinxiang Fu [6 ]
Jie Jin [7 ]
Jifeng Feng [8 ]
Xiaonan Hong [9 ]
Xiaohong Zhang [10 ]
Depei Wu [11 ]
Bin Jiang [12 ]
Xiaodong Dong [13 ]
机构
[1] National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing Key Laboratory of Clinical Study on Anticancer Molecular Targeted Drugs
[2] Harbin Medical University Cancer Hospital
[3] Fudan University Shanghai Cancer Center
[4] Jiangsu Cancer Hospital
[5] Peking University Third Hospital
[6] Tangdu Hospital of the Fourth Military Medical University
[7] The 307th Hospital of Military Chinese People’s Liberation Army
[8] The Second Affiliated Hospital of Soochow University
[9] The Second Affiliated Hospital Zhejiang University School of Medicine
[10] The First Affiliated Hospital Zhejiang University College of Medicine
[11] The First Affiliated Hospital of Soochow University
[12] Shanghai Henlius Biotech, Inc.
[13] Peking University People’s Hospital
关键词
Biosimilar; lymphoma; monoclonal antibody; pharmacokinetics; safety;
D O I
暂无
中图分类号
R733.1 [网状内皮系统肿瘤];
学科分类号
100214 ;
摘要
Objective: This study aimed to compare the pharmacokinetic, pharmacodynamic and safety profiles of HLX01(a rituximab biosimilar) and reference rituximab sourced from China(Mab Thera?; rituximab-CN).Methods: Here we report the results of two phase 1 studies. In the phase 1 a, open-label, dose-escalation study(NCT03218072, CTR20140400), eligible patients received 250, 375 and 500 mg/m2 HLX01 sequentially at 7-day intervals, after confirming no dose-limiting toxicity(DLT). In the phase 1 b, double-blind study(NCT02584920,CTR20140764), eligible patients were given a single dose of 375 mg/m2 HLX01 or rituximab-CN. The primary endpoints included safety and tolerability parameters for the phase 1 a and the area under the plasma concentrationtime curve from time zero to day 91(AUC0-91 d) for the phase 1 b study. Equivalence was concluded if 90%confidence interval(90% CI) for the geometric least squares mean ratio(GLSMR) fell in the pre-specified equivalence criteria(80%-125%).Results: Between June 20, 2014 and January 5, 2015, 12 patients were enrolled in the phase 1 a study. The pharmacokinetics of HLX01 showed dose proportionality and accumulation to steady state. HLX01 was well tolerated, with no serious adverse events(AEs), discontinuations or DLTs. Between November 8, 2014 and August13, 2015, 87 eligible patients were enrolled in the phase 1 b study, including 43 who received HLX01 and 44 who were treated with rituximab-CN. The equivalence endpoint was met with GLSMR for AUC0-91 d being 89.6%(90% CI: 80.4%-99.8%). AEs, anti-drug antibodies, and CD19+ and CD20+ B lymphocyte counts were similar between the HLX01 and rituximab-CN treatment groups.Conclusions: Treatment with HLX01 was safe and well tolerated in Chinese patients with B-cell lymphoma.HLX01 and rituximab-CN have similar pharmacokinetic, pharmacodynamic and safety profiles.
引用
收藏
页码:405 / 424
页数:20
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