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Physicochemical and functional assessments demonstrating analytical similarity between rituximab biosimilar HLX01 and the MabThera®
Development of bio-therapeutics has exhibited exponential growth in China over the past decade. However, no biosimilar drug has been approved in China (CN) due to the lack of a national biosimilar regulatory guidance. HLX01, a rituximab biosimilar developed in China under European Medicines Agency b...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6512903/ https://www.ncbi.nlm.nih.gov/pubmed/30794092 http://dx.doi.org/10.1080/19420862.2019.1578147 |
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author | Xu, Yanpeng Xie, Liqi Zhang, Erhui Gao, Wenyuan Wang, Linlin Cao, Yang Xie, Michael Hongwei Jiang, Weidong Liu, Scott |
author_facet | Xu, Yanpeng Xie, Liqi Zhang, Erhui Gao, Wenyuan Wang, Linlin Cao, Yang Xie, Michael Hongwei Jiang, Weidong Liu, Scott |
author_sort | Xu, Yanpeng |
collection | PubMed |
description | Development of bio-therapeutics has exhibited exponential growth in China over the past decade. However, no biosimilar drug has been approved in China (CN) due to the lack of a national biosimilar regulatory guidance. HLX01, a rituximab biosimilar developed in China under European Medicines Agency biosimilar guidelines and requirements, was the first such drug submitted for regulatory review in China, and it is expected to receive approval there as a biosimilar product. To demonstrate the analytical similarities of HLX01, CN-rituximab (sourced in China but manufactured in Europe) and EU-rituximab (sourced and manufactured in Europe), an extensive 3-way physicochemical and functional similarity assessment using a series of orthogonal and state-of-the-art techniques was conducted, following the similarity requirement guidelines recently published by China’s Center for Drug Evaluation. The results of the similarity study showed an identical protein amino acid sequence and highly similar primary structures between HLX01 and the reference product (RP) MabThera®, along with high similarities in higher order structures, potency, integrity, purity and impurity profiles, biological and immunological binding functions, as well as degradation behaviors under stress conditions. In addition, HLX01 presented slightly lower aggregates and better photostability compared with the RP. Despite slight changes in relative abundance of glycan moieties and heavy chain C-terminal lysine modification, no differences in biological activities and immunological properties were observed between the RP and HLX01. In conclusion, HLX01 is highly similar to CN- and EU-sourced RP in terms of physicochemical properties and biological activities, suggesting similar product quality, efficacy, and safety. The regulatory requirements interpreted and applied towards the HLX01 marketing application sets a precedent for analytical similarity assessment of biosimilar products in China. |
format | Online Article Text |
id | pubmed-6512903 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-65129032019-05-24 Physicochemical and functional assessments demonstrating analytical similarity between rituximab biosimilar HLX01 and the MabThera® Xu, Yanpeng Xie, Liqi Zhang, Erhui Gao, Wenyuan Wang, Linlin Cao, Yang Xie, Michael Hongwei Jiang, Weidong Liu, Scott MAbs Report Development of bio-therapeutics has exhibited exponential growth in China over the past decade. However, no biosimilar drug has been approved in China (CN) due to the lack of a national biosimilar regulatory guidance. HLX01, a rituximab biosimilar developed in China under European Medicines Agency biosimilar guidelines and requirements, was the first such drug submitted for regulatory review in China, and it is expected to receive approval there as a biosimilar product. To demonstrate the analytical similarities of HLX01, CN-rituximab (sourced in China but manufactured in Europe) and EU-rituximab (sourced and manufactured in Europe), an extensive 3-way physicochemical and functional similarity assessment using a series of orthogonal and state-of-the-art techniques was conducted, following the similarity requirement guidelines recently published by China’s Center for Drug Evaluation. The results of the similarity study showed an identical protein amino acid sequence and highly similar primary structures between HLX01 and the reference product (RP) MabThera®, along with high similarities in higher order structures, potency, integrity, purity and impurity profiles, biological and immunological binding functions, as well as degradation behaviors under stress conditions. In addition, HLX01 presented slightly lower aggregates and better photostability compared with the RP. Despite slight changes in relative abundance of glycan moieties and heavy chain C-terminal lysine modification, no differences in biological activities and immunological properties were observed between the RP and HLX01. In conclusion, HLX01 is highly similar to CN- and EU-sourced RP in terms of physicochemical properties and biological activities, suggesting similar product quality, efficacy, and safety. The regulatory requirements interpreted and applied towards the HLX01 marketing application sets a precedent for analytical similarity assessment of biosimilar products in China. Taylor & Francis 2019-02-22 /pmc/articles/PMC6512903/ /pubmed/30794092 http://dx.doi.org/10.1080/19420862.2019.1578147 Text en © 2019 The Author(s). Published with license by Taylor & Francis Group, LLC. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way. |
spellingShingle | Report Xu, Yanpeng Xie, Liqi Zhang, Erhui Gao, Wenyuan Wang, Linlin Cao, Yang Xie, Michael Hongwei Jiang, Weidong Liu, Scott Physicochemical and functional assessments demonstrating analytical similarity between rituximab biosimilar HLX01 and the MabThera® |
title | Physicochemical and functional assessments demonstrating analytical similarity between rituximab biosimilar HLX01 and the MabThera® |
title_full | Physicochemical and functional assessments demonstrating analytical similarity between rituximab biosimilar HLX01 and the MabThera® |
title_fullStr | Physicochemical and functional assessments demonstrating analytical similarity between rituximab biosimilar HLX01 and the MabThera® |
title_full_unstemmed | Physicochemical and functional assessments demonstrating analytical similarity between rituximab biosimilar HLX01 and the MabThera® |
title_short | Physicochemical and functional assessments demonstrating analytical similarity between rituximab biosimilar HLX01 and the MabThera® |
title_sort | physicochemical and functional assessments demonstrating analytical similarity between rituximab biosimilar hlx01 and the mabthera® |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6512903/ https://www.ncbi.nlm.nih.gov/pubmed/30794092 http://dx.doi.org/10.1080/19420862.2019.1578147 |
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