Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 1997 Jun 15;16(11):1241-57; discussion 1257-62.
doi: 10.1002/(sici)1097-0258(19970615)16:11<1241::aid-sim527>3.0.co;2-c.

Comparison of population pharmacokinetic modeling methods using simulated data: results from the Population Modeling Workgroup

Affiliations
Comparative Study

Comparison of population pharmacokinetic modeling methods using simulated data: results from the Population Modeling Workgroup

D J Roe. Stat Med. .

Abstract

Statistical modeling methods have had increasing use in drug disposition studies, both to estimate pharmacokinetic parameters and to develop regression models that relate these parameter estimates to patient characteristics. These methods are particularly flexible as they allow non-linearity and sparse within-patient information. In the past few years, multiple analysis methods have become available, but there is a lack of systematic comparisons of their estimates on the same data sets. Two simulated data sets were therefore developed by the Population Modeling Workgroup of the Biopharmaceutical Section of the American Statistical Association. We analysed these data sets using seven population modeling programs, some of which contain multiple analysis methods. Although each data set represents a single replicate from a given model and data collection design, the results suggest that the behaviour of some methods differs from that of the others.

PubMed Disclaimer

Publication types

LinkOut - more resources