Publication: Clinical Pharmacology in Drug Development
Abstract
Standard 1000-mg abiraterone acetate tablets, used with prednisone for metastatic prostate cancer, suffer from low and food-dependent bioavailability. This first-in-human, open-label, crossover Phase I trial evaluated RL001, a self-emulsifying soft-capsule abiraterone formulation designed to overcome these limitations, with plasma concentrations quantified by LC-MS/MS and pharmacokinetics modeled using Phoenix WinNonlin. A 200-mg dose of RL001 achieved abiraterone exposure exceeding that of the 1000-mg reference tablet while maintaining fed/fasted exposure ratios near 80% for AUC, effectively eliminating the food-related exposure spikes seen with the standard formulation; prednisone pharmacokinetics were unaffected, and hyperbilirubinemia and hypertriglyceridemia occurred less frequently. The findings suggest the abiraterone self-emulsifying soft capsule could offer a lower, more consistent therapeutic dose with an improved safety profile for prostate cancer patients.
Author(s): Yi M, Tu S, Cheng Z, Xia K
Published: January 1, 2026
Phoenix WinNonlin: Formulation Comparison at Scale
Phoenix WinNonlin modeled the exposure differences behind this abiraterone reformulation study, showing how a new capsule design overcame a known food-effect problem. As part of a Phoenix platform designed to move teams from data to decision in a fraction of the time, Phoenix WinNonlin remains the gold standard engine for noncompartmental analysis, PK/PD, and toxicokinetic modeling.


