Combining Therapeutic Drug Monitoring and Pharmacokinetic Modelling Deconvolutes Physiological and Environmental Sources of Variability in Clozapine Exposure

• Published in: Pharmaceutics Vol. 14; no. 1; p. 47
• Main Authors: Wills, Kenneth H, Behan, Stephen J, Nance, Michael J, Dawson, Jessica L, Polasek, Thomas M, Hopkins, Ashley M, van Dyk, Madelé, Rowland, Andrew
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 27.12.2021; MDPI
• Subjects: Age; Body mass index; Clinical medicine; clozapine; dose optimisation; Drug dosages; Enzyme kinetics; inter-individual variability; medication adherence; Metabolism; Metabolites; Patients; pharmacokinetic modelling; Pharmacokinetics; Physiology; Population; Psychotropic drugs; Simulation; therapeutic drug monitoring; clozapine; pharmacokinetic modelling; medication adherence; dose optimisation; therapeutic drug monitoring; inter-individual variability
• ISSN: 1999-4923; 1999-4923
• DOI: 10.3390/pharmaceutics14010047

Clozapine is a key antipsychotic drug for treatment-resistant schizophrenia but exhibits highly variable pharmacokinetics and a propensity for serious adverse effects. Currently, these challenges are addressed using therapeutic drug monitoring (TDM). This study primarily sought to (i) verify the importance of covariates identified in a prior clozapine population pharmacokinetic (popPK) model in the absence of environmental covariates using physiologically based pharmacokinetic (PBPK) modelling, and then to (ii) evaluate the performance of the popPK model as an adjunct or alternative to TDM-guided dosing in an active TDM population. A popPK model incorporating age, metabolic activity, sex, smoking status and weight was applied to predict clozapine trough concentrations (C ) in a PBPK-simulated population and an active TDM population comprising 142 patients dosed to steady state at Flinders Medical Centre in Adelaide, South Australia. Post hoc analyses were performed to deconvolute the impact of physiological and environmental covariates in the TDM population. Analysis of PBPK simulations confirmed age, cytochrome P450 1A2 activity, sex and weight as physiological covariates associated with variability in clozapine C (R = 0.7698; = 0.0002). Prediction of clozapine C using a popPK model based on these covariates accounted for <5% of inter-individual variability in the TDM population. Post hoc analyses confirmed that environmental covariates accounted for a greater proportion of the variability in clozapine C in the TDM population. Variability in clozapine exposure was primarily driven by environmental covariates in an active TDM population. Pharmacokinetic modelling can be used as an adjunct to TDM to deconvolute sources of variability in clozapine exposure.