PHARMACOKINETIC-PHARMACODYNAMIC RELATIONSHIPS IN PHASE-I PHASE-II OF DRUG DEVELOPMENT

被引:15
|
作者
VANPEER, A [1 ]
SNOECK, E [1 ]
HUANG, ML [1 ]
HEYKANTS, J [1 ]
机构
[1] JANSSEN RES FDN,DEPT DRUG METAB & PHARMACOKINET,BEERSE,BELGIUM
关键词
PHARMACOKINETIC-PHARMACODYNAMIC RELATIONSHIP; DRUG DEVELOPMENT; STEREOISOMERISM; METABOLISM; RISK PATIENTS; DRUG DELIVERY;
D O I
10.1007/BF03220008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Early investigation of pharmacokinetic-pharmacodynamic relationships in Phase I/II may facilitate the further clinical development of a new drug. Although some pharmacology assessments in Phase I are often only surrogates for the therapeutic effect, PK-PD modelling of those effects provides in general crucial information on the drug's potency in vivo. A mathematical PK-PD expression allows explorative simulations on the rate of onset of drug action, on the intensity and duration of the effects for doses in future clinical trials, or in situations of altered drug kinetics. Furthermore, understanding of the PK-PD relationship early on in drug development may anticipate unnecessary exposure of human subjects to inappropriate drug doses or trials.
引用
收藏
页码:49 / 59
页数:11
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