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药企间视角下的生物制药药物产品稳健性研究。

An Intercompany Perspective on Biopharmaceutical Drug Product Robustness Studies.

机构信息

Biopharmaceutical Product Sciences, GlaxoSmithKline R&D, 709 Swedeland Road, King of Prussia, Pennsylvania 19406.

Drug Product Science and Technology, Bristol-Myers Squibb, One Squibb Drive, New Brunswick, New Jersey 08903.

出版信息

J Pharm Sci. 2018 Feb;107(2):529-542. doi: 10.1016/j.xphs.2017.10.017. Epub 2017 Oct 23.

Abstract

The Biophorum Development Group (BPDG) is an industry-wide consortium enabling networking and sharing of best practices for the development of biopharmaceuticals. To gain a better understanding of current industry approaches for establishing biopharmaceutical drug product (DP) robustness, the BPDG-Formulation Point Share group conducted an intercompany collaboration exercise, which included a bench-marking survey and extensive group discussions around the scope, design, and execution of robustness studies. The results of this industry collaboration revealed several key common themes: (1) overall DP robustness is defined by both the formulation and the manufacturing process robustness; (2) robustness integrates the principles of quality by design (QbD); (3) DP robustness is an important factor in setting critical quality attribute control strategies and commercial specifications; (4) most companies employ robustness studies, along with prior knowledge, risk assessments, and statistics, to develop the DP design space; (5) studies are tailored to commercial development needs and the practices of each company. Three case studies further illustrate how a robustness study design for a biopharmaceutical DP balances experimental complexity, statistical power, scientific understanding, and risk assessment to provide the desired product and process knowledge. The BPDG-Formulation Point Share discusses identified industry challenges with regard to biopharmaceutical DP robustness and presents some recommendations for best practices.

摘要

生物制药开发小组(BPDG)是一个行业范围内的联盟,旨在促进生物制药开发方面的网络和最佳实践共享。为了更好地了解当前行业在建立生物制药产品(DP)稳健性方面的方法,BPDG-配方点共享小组进行了一次公司间合作的实践,包括基准调查和围绕稳健性研究的范围、设计和执行进行广泛的小组讨论。这次行业合作的结果揭示了几个关键的共同主题:(1)整体 DP 稳健性由配方和制造工艺稳健性共同定义;(2)稳健性整合了质量源于设计(QbD)的原则;(3)DP 稳健性是制定关键质量属性控制策略和商业规格的重要因素;(4)大多数公司采用稳健性研究,以及先验知识、风险评估和统计学,来开发 DP 设计空间;(5)研究根据商业开发需求和每家公司的实践进行调整。三个案例研究进一步说明了如何为生物制药 DP 的稳健性研究设计平衡实验复杂性、统计能力、科学理解和风险评估,以提供所需的产品和工艺知识。BPDG-配方点共享小组讨论了生物制药 DP 稳健性方面的行业挑战,并提出了一些最佳实践的建议。

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