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OptiMal-PK: an internet-based user-friendly interface for the mathematical-based design of optimized anti-malarial treatment regimens

机译:OptiMal-PK:基于互联网的用户友好界面用于基于数学的优化抗疟疾治疗方案设计

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摘要

BackgroundThe search for highly effective anti-malarial therapies has gathered pace and recent years have seen a number of promising single and combined therapies reach the late stages of development. A key drug development challenge is the need for early assessment of the clinical utility of new drug leads as it is often unclear for developers whether efforts should be focused on efficacy or metabolic stability/exposure or indeed whether the continuation of iterative QSAR (quantitative structure–activity and relationships) cycles of medicinal chemistry and biological testing will translate to improved clinical efficacy. Pharmacokinetic and pharmacodynamic (PK/PD)-based measurements available from in vitro studies can be used for such clinical predictions. However, these predictions often require bespoke mathematical PK/PD modelling expertise and are normally performed after candidate development and, therefore, not during the pre-clinical development phase when such decisions need to be made.
机译:背景技术寻求高效抗疟疾疗法的步伐不断加快,近年来,许多有前途的单一疗法和联合疗法已进入发展后期。药物开发面临的一项关键挑战是需要及早评估新药线索的临床实用性,因为开发人员通常不清楚应将精力集中在功效还是代谢稳定性/暴露上,还是应该继续进行迭代QSAR(定量结构–活性和相关性)的化学和生物学测试周期将转化为改善的临床疗效。可从体外研究获得的基于药代动力学和药效学(PK / PD)的测量可用于此类临床预测。但是,这些预测通常需要量身定制的数学PK / PD建模专业知识,并且通常在候选人开发后进行,因此不在需要做出此类决定的临床前开发阶段进行。

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