临床药物开发中的新研究设计。

Olli Tenhunen, Miia Turpeinen, Pekka Kurki
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引用次数: 0

摘要

一种新药的临床开发传统上被视为一系列的四个阶段,每个阶段在确定药物的有效性和安全性方面都有自己的目标。日益个性化的医疗和药物作用机制的变化也改变了临床药物测试的设计。发展阶段的边界变得模糊,传统的大型、受控的多中心研究可能部分被个人和基于风险的方法所取代。从生物学的角度出发,药物的适应症更加精确,以目标为导向的发展可以指导临床试验的各个阶段的设计。在临床药物测试中,利用注册表中的数据以及建模将变得更加普遍。
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New study designs in clinical drug development.

Clinical development of a novel drug has traditionally been seen as a series of four phases, each having its own objectives in establishing the efficacy and safety of the drug. Increasingly individualized medicine and the changing mechanisms of drug action are also changing the designs of clinical drug testing. The borders of development phases become blurred and the traditional large, controlled multicenter studies may in part be replaced by individual and risk-based approaches. The indications for drugs are more precisely targeted from biological starting points, and a target-oriented development may guide the designs of clinical testing at all stages of development. Utilization of data from registries along with modeling will become more common in clinical drug testing.

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