A PBPK study showed an increasing trend in t 1/2 , and a decreasing trend in CL z/F when acalabrutinib was co-administered with CYP3A inhibitors (fluconazole, isavuconazole) (Chen et al. 2022 ), as compared to acalabrutinib alone, which was consistent with the trend of our animal results.
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Inhibition of acalabrutinib metabolism by finerenone and its molecular docking studies.
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