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Host Cell Protein Clinical Safety Risk Assessment—An Updated Industry Review

生物制药 风险评估 鉴定(生物学) 风险分析(工程) 设计质量 产品(数学) 工艺安全 质量(理念) 新产品开发 过程(计算) 良好制造规范 业务 药物开发 计算机科学 医学 药品 工程类 生物技术 运营管理 在制品 药理学 监管事务 几何学 营销 哲学 操作系统 认识论 生物 植物 计算机安全 数学
作者
Lisette Coye,Marisa Jones,Georgeen Gaza‐Bulseco,Carmelata Chitikila,Séverine Clavier,Delphine Fougeron,Christine Grimaldi,Karen Hurkmans,Richard W. Hutchinson,Brenda Kellogg,Xinrong Liu,Nisha Palackal,Mahima Tank,Pascal Valax,Thomas Waerner,Fengqiang Wang,Zhang Ying,Yiwei Zhao,S Sloan,Christina L. Zuch de Zafra
出处
期刊:Biotechnology and Bioengineering [Wiley]
卷期号:122 (11): 3229-3248
标识
DOI:10.1002/bit.70029
摘要

ABSTRACT Host cell proteins (HCP) are process‐related impurities that can co‐purify with therapeutic proteins. Some HCP impurities potentially can have an impact on patient safety (immunogenicity or toxicity), efficacy, and/or product quality. It is important to reduce the levels of HCP impurities with a well‐controlled manufacturing process and to monitor levels with a suitable analytical assay. Biopharmaceutical companies are now routinely using mass spectrometry to identify HCPs which are present in process intermediates and potentially in bulk drug substances and using the data to make decisions to continuously improve their processes and mitigate the potential risk to patients. Some companies perform identification of HCPs starting from the nonclinical stage of development, while others perform HCP identification at later stages or as a part of root cause analysis for identified HCP ELISA‐related issues, process, and product quality or safety concerns. No matter the approach, a comprehensive risk assessment framework for identified HCPs is needed to support decision‐making during development and is expected by regulators to ensure a safe and efficacious drug product. In this paper the BioPhorum Development Group HCP Workstream has brought together a team of industry experts to build upon existing risk assessment frameworks (e.g., de Zafra et al., 2015) and developed recommendations for assessment of clinical safety risks upon identification of individual HCPs, incorporating regulatory considerations and industry experience and using a real‐world case study to illustrate the use of the updated frameworks. Key recommendations include conducting clinical risk assessment alongside product quality risk assessment following individual HCP identification and quantitation; focusing on biological activity and immunogenicity for any HCPs of concern; and communicating and collaborating effectively across functions to enable a comprehensive risk assessment.
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