期刊
BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY
卷 96, 期 3, 页码 206-211出版社
BLACKWELL MUNKSGAARD
DOI: 10.1111/j.1742-7843.2005.pto960310.x
关键词
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For many oncological agents, myelosuppression is the dose-limiting toxicity and the quantitative characterisation of the relationship between drug dose, plasma concentration and haematological toxicity is of importance in the drug development. Mechanism-based population pharmacokinetic-pharmacodynamic models have been developed for this purpose and the applications of these in candidate selection, first-in-man studies, prodrug and formulation development, dose finding, schedule optimisation, assessing influence of modifying agents, drug combination studies, subgroup identification and feedback individualisation are reviewed.
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