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生物类似药的研发

Development of biosimilars.

作者信息

Al-Sabbagh Ahmad, Olech Ewa, McClellan Joseph E, Kirchhoff Carol F

机构信息

Development Group, Pfizer Global Established Pharma Medicines, New York, NY.

Department of Internal Medicine, University of Nevada School of Medicine, 1707 W Charleston Boulevard, Suite 220, Las Vegas, NV 89102.

出版信息

Semin Arthritis Rheum. 2016 Apr;45(5 Suppl):S11-8. doi: 10.1016/j.semarthrit.2016.01.002. Epub 2016 Jan 21.

Abstract

OBJECTIVE

To provide an overview of the underlying scientific principles and standards for developing a biosimilar product.

METHODS

An Internet-based literature search through June 2015 was performed for information related to biosimilar manufacturing and development, including a review of regulatory guidelines and requirements.

RESULTS

Biologics, both biosimilars and their corresponding reference products, are complex molecules produced by biotechnology in living systems. The development of biologics involves multiple levels of intricate, highly controlled manufacturing processes, combined with pre-clinical structural, functional, and biological assessments, as well as clinical efficacy and safety, including immunogenicity, analyses. In addition, to ensure a high degree of similarity, a biosimilar must undergo a comparability exercise at every step of its development, as outlined by regulatory agencies, to demonstrate that potential differences from the reference product are not clinically meaningful with regard to quality, safety, and efficacy [European Medicines Agency (EMA)] or safety, purity, and potency [US Food and Drug Administration (FDA)]. At the foundation of the biosimilar development process lays the establishment of a high degree of structural similarity with its reference product. State-of-the-art technologies must be employed to demonstrate a high degree of structural and functional similarity. Finally, clinical pharmacokinetic and pharmacodynamic as well as clinical efficacy and safety similarity must be confirmed between biosimilar and originator. Regulators, including the FDA and the EMA consider the totality of the evidence from this comprehensive step-wise comparative similarity exercise in its determination of biosimilarity for licensing.

CONCLUSIONS

The rigorous and highly regulated processes required to develop a biosimilar have been designed as such to establish a high degree of biosimilarity with a reference product in terms of the structural, functional, biological, and clinical attributes.

摘要

目的

概述开发生物类似药产品的基础科学原理和标准。

方法

通过互联网检索截至2015年6月与生物类似药生产和开发相关的信息,包括对监管指南和要求的综述。

结果

生物制品,包括生物类似药及其相应的参照产品,是通过生物技术在活体系统中产生的复杂分子。生物制品的开发涉及多个层次的复杂、高度受控的生产过程,同时还包括临床前的结构、功能和生物学评估,以及临床疗效和安全性分析,包括免疫原性分析。此外,为确保高度相似性,生物类似药在其开发的每个阶段都必须按照监管机构的要求进行可比性研究,以证明与参照产品在质量、安全性和疗效方面(欧洲药品管理局)或安全性、纯度和效力方面(美国食品药品监督管理局)的潜在差异在临床上无意义。生物类似药开发过程的基础是与其参照产品建立高度的结构相似性。必须采用先进技术来证明高度的结构和功能相似性。最后,必须确认生物类似药与原创药之间在临床药代动力学和药效学以及临床疗效和安全性方面的相似性。包括美国食品药品监督管理局和欧洲药品管理局在内的监管机构在确定生物类似药的许可时,会考虑这一全面的逐步比较相似性研究的全部证据。

结论

开发生物类似药所需的严格且高度规范的过程旨在使其在结构、功能、生物学和临床属性方面与参照产品建立高度的生物相似性。

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