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Analysis of non-mutagenic substances in the context of drug impurity assessment – Few are potent toxicants

效力 化学 药品 背景(考古学) 药理学 毒理 色谱法 医学 生物化学 体外 生物 古生物学
作者
Catrin Hasselgren,Michelle Kenyon,Lennart T. Anger,Paul D. Cornwell,Eric D. Watt,Joel P. Bercu
出处
期刊:Regulatory Toxicology and Pharmacology [Elsevier BV]
卷期号:150: 105645-105645 被引量:6
标识
DOI:10.1016/j.yrtph.2024.105645
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 2815 compounds were evaluated, of which 2213 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.
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