群体PK模型作为生物等效性的替代途径

Parmesh Gajjar, Jake Dickinson, Harri Dickinson, Linette Ruston, Hitesh B. Mistry, Claire Patterson, P. Dickinson
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引用次数: 0

摘要

证明生物等效性(BE)对于低成本仿制药的开发和批准提交后生产变更非常重要。然而,对于许多复杂的肠外产品,BE演示可能非常具有挑战性。例如,长效注射产品被设计为具有数周或数月的延长释放期,但这也意味着传统的BE研究可能需要数月或数年才能完成。在这里,我们总结了如何利用群体PK模型来研究数百种虚拟配方,从而确定在多次和单次给药后具有生物等效性的一系列产品,该模型捕获了由于群体变化而导致的PK谱差异。这为制定方案提供了指导,但也为BE评估开辟了其他更精简的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Population PK modelling as an alternative route to bioequivalence
Demonstratingbioequivalence (BE) is important for the development of lower cost genericproducts, and also for approving post-submission manufacturing changes.However, for many complex parenteral products, BE demonstration can be verychallenging. For example, long-acting injectable products are engineered tohave an extended release over several weeks or months, but this also means thata traditional BE study can take many months or years to perform. Here, we summarisehow population PK modelling, which captures differences in PK profiles due topopulation variation, could be used explore hundreds of virtual formulations,and thus determine a range of products that are bioequivalent after bothmultiple and single dosing. This provides a guide for formulation developmentbut also opens alternative, more streamlined routes to BE assessment. 
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