Biopharmaceutics & Drug Disposition · 2010 · 21 citations · 19 references
PharmacyPharmacokineticsPharmacologyPharmacodynamicsPharmacokinetic ModelingPharmacokinetic-pharmacodynamic ModelingModel BuildingModel EvaluationPharmacokinetic SimulationPharmacokinetic Parameter AnalysisPharmacokinetic ParametersPharmacokinetic-pharmacodynamic Link ModelingPk Model BuildingRate ConstantsSimultaneous Pharmacokinetic-pharmacodynamic ModelingSphingosine 1-Phosphate Receptor ModulationSphingosine Metabolism
The pharmacokinetic (PK) and pharmacodynamic (PD) parameters of ONO-4641 in humans were estimated using preclinical data in order to provide essential information to better design future clinical studies. The characterization of PK/PD was measured in terms of decreased lymphocyte counts in blood after administration of ONO-4641, a sphingosine 1-phosphate receptor modulator. Using a two-compartment model, human PK parameters were estimated from preclinical PK data of cynomolgus monkey and in vitro human metabolism data. To estimate human PD parameters, the relationship between lymphocyte counts and plasma concentrations of ONO-4641 in cynomolgus monkeys was determined. The relationship between lymphocyte counts and plasma concentrations of ONO-4641 was described by an indirect-response model. The indirect-response model had an I(max) value of 0.828 and an IC(50) value of 1.29 ng/ml based on the cynomolgus monkey data. These parameters were used to represent human PD parameters for the simulation of lymphocyte counts. Other human PD parameters such as input and output rate constants for lymphocytes were obtained from the literature. Based on these estimated human PK and PD parameters, human lymphocyte counts after administration of ONO-4641 were simulated. In conclusion, the simulation of human lymphocyte counts based on preclinical data led to the acquisition of useful information for designing future clinical studies.
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