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Manufacturing of [C-14]-Labeled Drug Substance and Drug Product Utilized in Clinical Research: A Case Study of Omecamtiv Mecarbil

机译:用于临床研究的[C-14]标记药物和药物产品的制造:以Omecamtiv Mecarbil为例

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摘要

This mini-review describes the Chemistry, Manufacturing and Control activities associated with the manufacture of [C-14]-labeled drug substance and subsequent drug compounding activities to generate clinical trial material utilized in human absorption, distribution, metabolism, and excretion clinical studies. Due to the unstable nature and increased decomposition rates observed with [C-14]-labeled compounds, the manufacture, testing, release, formulation, and regulatory filings are uniquely challenging. A case study of the cardiac myosin activator AMG 423 (omecamtiv mercarbil), utilized in a dual oral/intravenous infusion clinical study is presented.
机译:这份小型综述描述了与[C-14]标记药物的制造相关的化学,制造和控制活动,以及随后的药物合成活动,以产生用于人体吸收,分布,代谢和排泄临床研究的临床试验材料。由于使用[C-14]标记的化合物观察到不稳定的性质和增加的分解速率,因此制造,测试,释放,配制和监管文件具有独特的挑战性。本文介绍了在双重口服/静脉输注临床研究中使用的心肌肌球蛋白激活剂AMG 423(omecamtiv巯基)的案例研究。

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