首页> 外文期刊>Cancer Chemotherapy and Pharmacology >Toxicology and pharmacokinetic study of orally administered 5-iodo-2-pyrimidinone-2′deoxyribose (IPdR) × 28 days in Fischer-344 rats: impact on the initial clinical phase I trial design of IPdR-mediated radiosensitization
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Toxicology and pharmacokinetic study of orally administered 5-iodo-2-pyrimidinone-2′deoxyribose (IPdR) × 28 days in Fischer-344 rats: impact on the initial clinical phase I trial design of IPdR-mediated radiosensitization

机译:在Fischer-344大鼠中口服5-碘-2-嘧啶酮-2'脱氧核糖(IPdR)×28天的毒理学和药代动力学研究:对IPdR介导的放射增敏的初始临床I期试验设计的影响

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摘要

A toxicology and pharmacokinetic study of orally administered (po) IPdR (5-3iodo-2-pyrimidinone-2′deoxyribose, NSC-726188) was performed in Fischer-344 rats using a once daily (qd) × 28 days dosing schedule as proposed for an initial phase I clinical trial of IPdR as a radiosensitizer.
机译:在Fischer-344大鼠中进行了口服(po)IPdR(5-3碘-2-嘧啶酮-2'脱氧核糖,NSC-726188)的毒理学和药代动力学研究,建议的每日一次(qd)×28天给药方案用于IPdR作为放射增敏剂的第一阶段临床试验。

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