谷歌浏览器插件
订阅小程序
在清言上使用

Analysis of Non-Mutagenic Substances in the Context of Drug Impurity Assessment – Few Are Potent Toxicants

Regulatory toxicology and pharmacology(2024)

引用 0|浏览10
暂无评分
摘要
ICH Q3A/B guidelines provide qualification thresholds for impurities or degradation products in new drug substances and products. However, the guidelines note that certain impurities / degradation products may warrant further safety evaluation for being unusually potent or toxic. The purpose of this study was to confirm that especially toxic non-mutagenic compounds are rare and to identify classes of compounds that could warrant lower qualification thresholds. A total of 2,815 compounds were evaluated, of which 2,213 were assessed as non-mutagenic. For the purpose of this analysis, compounds were considered potent when the point of departure was ≤ 0.2 mg/kg/day based on the qualification threshold (1 mg/day or 0.02 mg/kg/day for a 50 kg human) in a new drug substance, with an additional 10-fold margin. Only 54 of the entire set (2.4%) would be considered potent based on this conservative potency analysis, confirming that the existing ICH Q3A/B qualification thresholds are appropriate for the majority of impurities. If the Q3A/B threshold, without the additional 10-fold margin is used, 14 compounds (0.6%) are considered “highly potent”. Very few non-mutagenic structural classes were identified, including organothiophosphates and derivatives, polychlorinated benzenes and polychlorinated polycyclic aliphatics, that correlate with potential high potency, consistent with prior publications.
更多
查看译文
关键词
Non-mutagenic,Impurities,Qualification,Drug substance,In silico,ICH Q3A,ICH Q3B,Drug product
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要