Journal article
Optimal designs for population pharmacokinetic studies of oral artesunate in patients with uncomplicated falciparum malaria
KM Jamsen, SB Duffull, J Tarning, N Lindegardh, N White, JA Simpson
Malaria Journal | BMC | Published : 2011
Abstract
Background: Currently, population pharmacokinetic (PK) studies of anti-malarial drugs are designed primarily by the logistical and ethical constraints of taking blood samples from patients, and the statistical models that are fitted to the data are not formally considered. This could lead to imprecise estimates of the target PK parameters, and/or designs insufficient to estimate all of the parameters. Optimal design methodology has been developed to determine blood sampling schedules that will yield precise parameter estimates within the practical constraints of sampling the study populations. In this work optimal design methods were used to determine sampling designs for typical future popu..
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Grants
Awarded by Wellcome Trust
Funding Acknowledgements
This work was funded by a project grant from the National Health and Medical Research Council (NHMRC; 566855). KMJ is funded by a NHMRC PhD scholarship. The Mahidol-Oxford Tropical Medicine Research Unit and the PKPDia collaboration are supported by the Wellcome Trust. We would like to thank Prof Richard Price from the Menzies School of Health Research, Darwin, Australia for reviewing the survey that was emailed to the malaria researchers.