首页> 美国卫生研究院文献>CPT: Pharmacometrics Systems Pharmacology >A Mechanistic Model of Drug-Induced Liver Injury Aids the Interpretation of Elevated Liver Transaminase Levels in a Phase I Clinical Trial
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A Mechanistic Model of Drug-Induced Liver Injury Aids the Interpretation of Elevated Liver Transaminase Levels in a Phase I Clinical Trial

机译:药物诱发的肝损伤的机理模型有助于对I期临床试验中肝转氨酶水平升高的解释

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摘要

Entolimod (CBLB502) is a Toll-like receptor 5 agonist in development as a single-dose countermeasure against total body irradiation. Efficacy can be assessed from animal studies, but the “Animal Rule” does not apply to safety assessment. Marked elevations of serum aminotransferases (exceeding 1,000 IU/l) were observed in some human subjects receiving Entolimod in a safety study, threatening its continued development. The percentage of total hepatocytes undergoing necrosis in these subjects was estimated using a mechanistic, multiscale, mathematical model (DILIsym). The simulations suggested that no subject in the safety study experienced more than a modest loss of hepatocytes (<5%), which was comparable to estimates from a study of healthy volunteers receiving treatment with heparins. The predicted hepatocyte loss with Entolimod was lower than that required to cause liver dysfunction or that is routinely excised from volunteers donating for autologous liver transplantation and did not likely represent a serious health risk.
机译:Entolimod(CBLB502)是一种Toll样受体5激动剂,正在开发中,作为针对全身辐射的单剂量对策。可以通过动物研究评估疗效,但“动物法则”不适用于安全性评估。在一项安全性研究中,在接受恩替莫特的一些人类受试者中观察到血清氨基转移酶显着升高(超过1,000 IU / l),威胁到其继续发展。使用机械,多尺度,数学模型(DILIsym)估算这些受试者中发生坏死的总肝细胞百分比。模拟表明,安全性研究中没有受试者的肝细胞损失不超过适度(<5%),这与接受肝素治疗的健康志愿者的研究估计值相当。预计使用恩替莫特治疗的肝细胞损失低于引起肝功能障碍所需的损失,或者是从为自体肝移植捐献的志愿者中常规切除的,并且可能不会构成严重的健康风险。

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