ArticleScientific reports2026
PBPK modeling predicts rilzabrutinib dose adjustments using BTK occupancy for CYP3A4 interactions and hepatic impairment.
Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
This study aimed to develop and validate a population-based physiologically-based pharmacokinetic (PBPK) model for the Bruton's tyrosine kinase inhibitor rilzabrutinib (RIL) to predict its pharmacokinetic (PK) and BTK occupancy (BO) profiles under various scenarios, including drug-drug interactions (DDIs) with CYP3A4 modulators and in patients with hepatic impairment. A PBPK model for RIL was constructed using PK data, BO parameters, and interaction parameters. The model was validated against clinical PK parameters (AUC and C
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