“High‐risk” host cell proteins (HCPs): A multi‐company collaborative view

生物制药 过程(计算) 风险分析(工程) 产品(数学) 风险评估 担心 生物 业务 过程管理 计算机科学 生物技术 医学 计算机安全 操作系统 数学 精神科 焦虑 几何学
作者
Marisa Jones,Nisha Palackal,Fengqiang Wang,Georgeen Gaza‐Bulseco,Karen Hurkmans,Yiwei Zhao,Carmelata Chitikila,Séverine Clavier,Suli Liu,Emily Menesale,Nicole S. Schonenbach,Satish Kumar Sharma,Pascal Valax,Thomas Waerner,Lei Zhang,Trish Connolly
出处
期刊:Biotechnology and Bioengineering [Wiley]
卷期号:118 (8): 2870-2885 被引量:102
标识
DOI:10.1002/bit.27808
摘要

Host cell proteins (HCPs) are process-related impurities that may copurify with biopharmaceutical drug products. Within this class of impurities there are some that are more problematic. These problematic HCPs can be considered high-risk and can include those that are immunogenic, biologically active, or enzymatically active with the potential to degrade either product molecules or excipients used in formulation. Some have been shown to be difficult to remove by purification. Why should the biopharmaceutical industry worry about these high-risk HCPs? What approach could be taken to understand the origin of its copurification and address these high-risk HCPs? To answer these questions, the BioPhorum Development Group HCP Workstream initiated a collaboration among its 26-company team with the goal of industry alignment around high-risk HCPs. The information gathered through literature searches, company experiences, and surveys were used to compile a list of frequently seen problematic/high-risk HCPs. These high-risk HCPs were further classified based on their potential impact into different risk categories. A step-by-step recommendation is provided for establishing a comprehensive control strategy based on risk assessments for monitoring and/or eliminating the known impurity from the process that would be beneficial to the biopharmaceutical industry.
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