Institute for Clinical Pharmacodynamics, United States.
Curr Opin Pharmacol. 2017 Oct;36:1-7. doi: 10.1016/j.coph.2017.06.002. Epub 2017 Jul 5.
My thesis is a simple one. We have not been doing a good enough job selecting dose regimens for serious infections during the drug development process. If we are to do a better job in the future, we need to revisit some uncomfortable places. That is, some notable program failures. To be clear, we are not revisiting program failures to make anyone uncomfortable or cast aspersions - but rather so that we sow the seeds for a better future. To that end, we will examine program failures and successes through a pharmacometric lens. Through this powerful lens, we will come to understand that many of our failures were not only predictable, but perhaps expected and entirely avoidable. The goal of this communication is to set forth the type of thinking and data that is necessary for rational dose selection.
我的论点很简单。在药物开发过程中,我们在为严重感染选择剂量方案方面做得还不够好。如果我们将来要做得更好,我们需要重新审视一些令人不安的地方。也就是说,一些值得注意的项目失败。需要明确的是,我们重新审视项目失败并不是为了让任何人感到不适或受到指责——而是为了为更美好的未来播下种子。为此,我们将通过药物计量学的视角来审视项目的失败和成功。通过这个强大的视角,我们将逐渐明白,我们的许多失败不仅是可以预测的,而且也许是可以预见的,并且完全可以避免的。本通讯的目的是提出进行合理剂量选择所需的思维和数据类型。