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药物监管中的临床药理学家:美国视角

The clinical pharmacologist in drug regulation: the US perspective.

作者信息

Temple R J

机构信息

Office of Drug Evaluation I, Food and Drug Administration, Rockville, MD 20852, USA.

出版信息

Br J Clin Pharmacol. 1996 Jul;42(1):73-9.

PMID:8807147
Abstract
  1. Drug development has moved into a new era--a time of particular interest in individualization of treatment and dose-response--that is of particular interest to clinical pharmacologists. 2. Clinical pharmacologists' skills are especially applicable to identifying subgroup differences in pharmacokinetics and the consequences of those differences through such techniques as the pharmacokinetic screen and evaluation of metabolic differences and drug-drug interactions. Clinical pharmacologists also can contribute to the discovery of true differences in pharmacodynamic response. 3. Clinical pharmacologists are trained to take a broad view of drugs, recognizing that they not only have the pharmacologic property of primary interest but often other properties as well, that a 'drug' is really many drugs (isomers, active metabolites) with different properties, and that the properties of drugs should affect how they are dosed and used.
摘要
  1. 药物研发已进入一个新时代——一个对治疗个体化和剂量反应特别感兴趣的时代——这对临床药理学家来说尤为重要。2. 临床药理学家的技能特别适用于通过药代动力学筛选、代谢差异评估和药物相互作用等技术来识别药代动力学中的亚组差异以及这些差异的后果。临床药理学家还可以为发现药效学反应中的真正差异做出贡献。3. 临床药理学家接受的培训是从广泛的角度看待药物,认识到药物不仅具有主要关注的药理特性,而且往往还具有其他特性,一种“药物”实际上是许多具有不同特性的药物(异构体、活性代谢物),并且药物的特性应该影响其给药和使用方式。

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