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Physiologically‐based pharmacokinetic modelling to predict oprozomib CYP3A drug–drug interaction potential in patients with advanced malignancies
Author(s) -
Ou Ying,
Xu Yang,
Gore Lia,
Harvey R. Donald,
Mita Alain,
Papadopoulos Kyriakos P.,
Wang Zhengping,
Cutler Richard E.,
Pinchasik Dawn E.,
Tsimberidou Apostolia M.
Publication year - 2019
Publication title -
british journal of clinical pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.216
H-Index - 146
eISSN - 1365-2125
pISSN - 0306-5251
DOI - 10.1111/bcp.13817
Subject(s) - physiologically based pharmacokinetic modelling , cyp3a4 , pharmacokinetics , pharmacology , drug , medicine , drug metabolism , adverse effect , drug development , clinical significance , cyp3a , cytochrome p450 , oncology , metabolism
Aims Oprozomib is an oral, second‐generation, irreversible proteasome inhibitor currently in clinical development for haematologic malignancies, including multiple myeloma and other malignancies. Oprozomib is a rare example of a small molecule drug that demonstrates cytochrome P450 (CYP) mRNA suppression. This unusual property elicits uncertainty regarding the optimal approach for predicting its drug–drug interaction (DDI) risk. The current study aims to understand DDI potential during early clinical development of oprozomib. Methods To support early development of oprozomib (e.g. inclusion/exclusion criteria, combination study design), we used human hepatocyte data and physiologically‐based pharmacokinetic (PBPK) modelling to predict its CYP3A4‐mediated DDI potential. Subsequently, a clinical DDI study using midazolam as the substrate was conducted in patients with advanced malignancies. Results The clinical DDI study enrolled a total of 21 patients, 18 with advanced solid tumours. No patient discontinued oprozomib due to a treatment‐related adverse event. The PBPK model prospectively predicted oprozomib 300 mg would not cause a clinically relevant change in exposure to CYP3A4 substrates (≤30%), which was confirmed by the results of this clinical DDI study. Conclusions These results indicate oprozomib has a low potential to inhibit the metabolism of CYP3A4 substrates in humans. The study shows that cultured human hepatocytes are a more reliable system for DDI prediction than human liver microsomes for studying this class of compounds. Developing a PBPK model prior to a clinical DDI study has been valuable in supporting clinical development of oprozomib.