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Model-Based Drug Development: The Road to Quantitative Pharmacology

机译:基于模型的药物开发:定量药理学之路

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High development costs and low success rates in bringing new medicines to the market demand more efficient and effective approaches. Identified by the FDA as a valuable prognostic tool for fulfilling such a demand, model-based drug development is a mathematical and statistical approach that constructs, validates, and utilizes disease models, drug exposure-response models, and pharmacometric models to facilitate drug development. Quantitative pharmacology is a discipline that learns and confirms the key characteristics of new molecular entities in a quantitative manner, with goal of providing explicit, reproducible, and predictive evidence for optimizing drug development plans and enabling critical decision making. Model-based drug development serves as an integral part of quantitative pharmacology. This work reviews the general concept, basic elements, and evolving role of model-based drug development in quantitative pharmacology. Two case studies are presented to illustrate how the model-based drug development approach can facilitate knowledge management and decision making during drug development. The case studies also highlight the organizational learning that comes through implementation of quantitative pharmacology as a discipline. Finally, the prospects of quantitative pharmacology as an emerging discipline are discussed. Advances in this discipline will require continued collaboration between academia, industry and regulatory agencies.
机译:将新药推向市场的高昂开发成本和低成功率需要更有效的方法。基于FDA的开发认为,基于模型的药物开发是一种数学和统计方法,可构建,验证和利用疾病模型,药物暴露反应模型和药理模型来促进药物开发,是FDA认为是满足此类需求的有价值的预后工具。定量药理学是一门以定量方式学习和确认新分子实体的关键特征的学科,目的是提供明确,可再现和可预测的证据,以优化药物开发计划并支持关键决策。基于模型的药物开发是定量药理学的组成部分。这项工作回顾了基于模型的药物开发在定量药理学中的一般概念,基本要素和不断发展的作用。提出了两个案例研究,以说明基于模型的药物开发方法如何促进药物开发过程中的知识管理和决策。案例研究还强调了通过实施定量药理学作为一门学科的组织学习。最后,讨论了定量药理学作为一门新兴学科的前景。该学科的进步将需要学术界,行业和监管机构之间的持续合作。

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