Model-Informed Drug Development for Everolimus Dosing Selection in Pediatric Infant Patients

CPT Pharmacometrics Syst Pharmacol. 2020 Apr;9(4):230-237. doi: 10.1002/psp4.12502. Epub 2020 Apr 5.

Abstract

Everolimus is currently approved in Europe as an adjunctive therapy for patients aged ≥ 2 years with tuberous sclerosis complex (TSC)-associated treatment-refractory partial-onset seizures, based on the EXIST-3 study (NCT01713946) results. As TSC-associated seizures can also affect children aged between 6 months and 2 years, a modeling and simulation (M&S) approach was undertaken to extrapolate exposure (trough plasma concentration (Cmin )) after a dose of 6 mg/m2 and reduction in seizure frequency (RSF). A physiologically based pharmacokinetic model using Simcyp was developed to predict Cmin in adult and pediatric patients, which was then used by a population pharmacodynamic model and a linear mixed effect model to predict short-term and long-term efficacy in adults (for validation) and in children, respectively. Based on the results of the M&S study, everolimus at the dose of 6 mg/m2 is anticipated to be an efficacious treatment in children 6 months to 2 years of age (up to 77.8% RSF) with concentrations within the recommended target range.

Publication types

  • Research Support, Non-U.S. Gov't
  • Validation Study

MeSH terms

  • Adult
  • Age Factors
  • Child, Preschool
  • Computer Simulation
  • Dose-Response Relationship, Drug
  • Drug Development / methods
  • Everolimus / administration & dosage*
  • Everolimus / pharmacokinetics
  • Humans
  • Infant
  • Models, Biological*
  • Seizures / drug therapy*
  • Seizures / etiology
  • Time Factors
  • Tuberous Sclerosis / complications
  • Tuberous Sclerosis / drug therapy*

Substances

  • Everolimus