Publication: Frontiers in Pharmacology
Abstract
TQ-B3203 is a novel topoisomerase I inhibitor liposome injection in development for advanced solid tumors, showing considerable inter-patient pharmacokinetic variability in early clinical testing. This study used plasma concentrations from a Phase I trial in Chinese patients to build a population pharmacokinetic model with Phoenix NLME, screening for covariates affecting drug disposition. Direct bilirubin and body mass index were the most influential covariates on clearance, while lean body weight affected the central compartment's volume of distribution, with model simulations confirming clinically meaningful effects on exposure. This first robust population pharmacokinetic model for TQ-B3203 provides a reference for future dose regimen decisions in its continued clinical development.
Author(s): Li X, Bo Y, Yin H, Liu X, Li X, Yang F
Published: January 16, 2023
Phoenix NLME: First Model for a Liposomal Therapy
Phoenix NLME built the first population PK model for this liposomal topoisomerase inhibitor, screening covariates to explain wide inter-patient variability. Phoenix NLME can be paired with Modeling Assistant, an AI copilot for model building and PML authoring, as part of a Phoenix platform that has trained more than 9,000 people.


