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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

OBJECTIVE: This study aimed to compare the pharmacokinetic, pharmacodynamic and safety profiles of HLX01 (a rituximab biosimilar) and reference rituximab sourced from China (MabThera(®); rituximab-CN). METHODS: Here we report the results of two phase 1 studies. In the phase 1a, open-label, dose-esca...

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Autores principales: Shi, Yuankai, Zhang, Qingyuan, Han, Xiaohong, Qin, Yan, Ke, Xiaoyan, Su, Hang, Liu, Li, Fu, Jinxiang, Jin, Jie, Feng, Jifeng, Hong, Xiaonan, Zhang, Xiaohong, Wu, Depei, Jiang, Bin, Dong, Xiaodong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8286892/
https://www.ncbi.nlm.nih.gov/pubmed/34321836
http://dx.doi.org/10.21147/j.issn.1000-9604.2021.03.11
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author Shi, Yuankai
Zhang, Qingyuan
Han, Xiaohong
Qin, Yan
Ke, Xiaoyan
Su, Hang
Liu, Li
Fu, Jinxiang
Jin, Jie
Feng, Jifeng
Hong, Xiaonan
Zhang, Xiaohong
Wu, Depei
Jiang, Bin
Dong, Xiaodong
author_facet Shi, Yuankai
Zhang, Qingyuan
Han, Xiaohong
Qin, Yan
Ke, Xiaoyan
Su, Hang
Liu, Li
Fu, Jinxiang
Jin, Jie
Feng, Jifeng
Hong, Xiaonan
Zhang, Xiaohong
Wu, Depei
Jiang, Bin
Dong, Xiaodong
author_sort Shi, Yuankai
collection PubMed
description OBJECTIVE: This study aimed to compare the pharmacokinetic, pharmacodynamic and safety profiles of HLX01 (a rituximab biosimilar) and reference rituximab sourced from China (MabThera(®); rituximab-CN). METHODS: Here we report the results of two phase 1 studies. In the phase 1a, open-label, dose-escalation study (NCT03218072, CTR20140400), eligible patients received 250, 375 and 500 mg/m(2) HLX01 sequentially at 7-day intervals, after confirming no dose-limiting toxicity (DLT). In the phase 1b, double-blind study (NCT02584920, CTR20140764), eligible patients were given a single dose of 375 mg/m(2) HLX01 or rituximab-CN. The primary endpoints included safety and tolerability parameters for the phase 1a and the area under the plasma concentration-time curve from time zero to day 91 (AUC(0−91 d)) for the phase 1b 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 1a 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 August 13, 2015, 87 eligible patients were enrolled in the phase 1b study, including 43 who received HLX01 and 44 who were treated with rituximab-CN. The equivalence endpoint was met with GLSMR for AUC(0−91 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.
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spelling pubmed-82868922021-07-27 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 Shi, Yuankai Zhang, Qingyuan Han, Xiaohong Qin, Yan Ke, Xiaoyan Su, Hang Liu, Li Fu, Jinxiang Jin, Jie Feng, Jifeng Hong, Xiaonan Zhang, Xiaohong Wu, Depei Jiang, Bin Dong, Xiaodong Chin J Cancer Res Original Article OBJECTIVE: This study aimed to compare the pharmacokinetic, pharmacodynamic and safety profiles of HLX01 (a rituximab biosimilar) and reference rituximab sourced from China (MabThera(®); rituximab-CN). METHODS: Here we report the results of two phase 1 studies. In the phase 1a, open-label, dose-escalation study (NCT03218072, CTR20140400), eligible patients received 250, 375 and 500 mg/m(2) HLX01 sequentially at 7-day intervals, after confirming no dose-limiting toxicity (DLT). In the phase 1b, double-blind study (NCT02584920, CTR20140764), eligible patients were given a single dose of 375 mg/m(2) HLX01 or rituximab-CN. The primary endpoints included safety and tolerability parameters for the phase 1a and the area under the plasma concentration-time curve from time zero to day 91 (AUC(0−91 d)) for the phase 1b 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 1a 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 August 13, 2015, 87 eligible patients were enrolled in the phase 1b study, including 43 who received HLX01 and 44 who were treated with rituximab-CN. The equivalence endpoint was met with GLSMR for AUC(0−91 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. AME Publishing Company 2021-06-30 /pmc/articles/PMC8286892/ /pubmed/34321836 http://dx.doi.org/10.21147/j.issn.1000-9604.2021.03.11 Text en Copyright ©2021Chinese Journal of Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-sa/4.0/This work is licensed under a Creative Commons Attribution-Non Commercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ (https://creativecommons.org/licenses/by-nc-sa/4.0/)
spellingShingle Original Article
Shi, Yuankai
Zhang, Qingyuan
Han, Xiaohong
Qin, Yan
Ke, Xiaoyan
Su, Hang
Liu, Li
Fu, Jinxiang
Jin, Jie
Feng, Jifeng
Hong, Xiaonan
Zhang, Xiaohong
Wu, Depei
Jiang, Bin
Dong, Xiaodong
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
title 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
title_full 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
title_fullStr 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
title_full_unstemmed 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
title_short 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
title_sort 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
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8286892/
https://www.ncbi.nlm.nih.gov/pubmed/34321836
http://dx.doi.org/10.21147/j.issn.1000-9604.2021.03.11
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