Guidelines and pharmacopoeial standards for pharmaceutical impurities: Overview and critical assessment

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• 作者：David J. Snodin^a ; ^{snodind@xiphora.com} ; Sean D. McCrossen^b
• 关键词：Impurities ; Toxicology ; Genotoxic ; TTC ; Drug safety ; Risk assessment ; Analysis ; Pharmacopoeia ; ICH ; Guideline ; Qualification
• 刊名：Regulatory Toxicology and Pharmacology
• 出版年：2012
• 期刊代码：57_02732300
• 类别：pha
• 出版时间：July, 2012
• 卷：63
• 期：2
• 页码：298-312
• 文件大小：526 K

摘要

ICH/regional guidances and agency scrutiny provide the regulatory framework for safety assessment and control of impurities in small-molecule drug substances and drug products. We provide a critical assessment of the principal impurity guidances and, in particular, focus on deficiencies in the derivation of the threshold of toxicological concern (TTC) as applied to genotoxic impurities and the many toxicological anomalies generated by following the current guidelines on impurities. In terms of pharmacopoeial standards, we aim to highlight the fact that strictly controlling numerous impurities, especially those that are minor structural variants of the active substance, is likely to produce minimal improvements in drug safety. It is believed that, wherever possible, there is a need to simplify and rebalance the current impurity paradigm, moving away from standards derived largely from batch analytical data towards structure-based qualification thresholds and risk assessments using readily available safety data. Such changes should also lead to a minimization of in vivo testing for toxicological qualification purposes. Recent improvements in analytical techniques and performance have enabled the detection of ever smaller amounts of impurities with increased confidence. The temptation to translate this information directly to the regulatory sphere without any kind of safety evaluation should be resisted.