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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
 
 

A program for individual and population optimal design for univariate and multivariate response pharmacokinetic-pharmacodynamic models.

The design of pharmacokinetic and pharmacodynamic experiments concerns a number of issues, among which are the number of observations and the times when they are taken. Often a model is used to describe these data and the pharmacokinetic-pharmacodynamic behavior of a drug. Knowledge of the data analysis model at the design stage is beneficial for collecting patient data for parameter estimation. A number of criteria for model-oriented experiments, which maximize the information content of the data, are available. In this paper we present a program, Popdes, to investigate the D-optimal design of individual and population multivariate response models, such as pharmacokinetic-pharmacodynamic, physiologically based pharmacokinetic, and parent drug and metabolites models. A pre-clinical and clinical pharmacokinetic-pharmacodynamic model describing the concentration-time profile and effect of an oncology compound in development is used for illustration.[1]

References

  1. A program for individual and population optimal design for univariate and multivariate response pharmacokinetic-pharmacodynamic models. Gueorguieva, I., Ogungbenro, K., Graham, G., Glatt, S., Aarons, L. Comput. Methods. Programs. Biomed (2007) [Pubmed]
 
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