2022
DOI: 10.1080/10428194.2022.2150820
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A phase 1, open-label, randomized drug–drug interaction study of zanubrutinib with moderate or strong CYP3A inhibitors in patients with B-cell malignancies

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Cited by 3 publications
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“…6 In another DDI study in patients with B-cell malignancies, co-administration of zanubrutinib with the CYP3A inhibitor fluconazole resulted in 1.81-fold and 1.88fold increases in zanubrutinib C max and AUC 0-24 h , respectively, and co-administration of zanubrutinib with the CYP3A inhibitor diltiazem resulted in a 1.62fold increase for both C max and AUC 0-24 h . 12 Although the reduction of zanubrutinib exposures with the coadministration of a strong CYP3A inducer such as rifampin has been evaluated, the magnitude and extent of reduction with the co-administration of less potent CYP3A inducers is largely unknown.…”
mentioning
confidence: 99%
“…6 In another DDI study in patients with B-cell malignancies, co-administration of zanubrutinib with the CYP3A inhibitor fluconazole resulted in 1.81-fold and 1.88fold increases in zanubrutinib C max and AUC 0-24 h , respectively, and co-administration of zanubrutinib with the CYP3A inhibitor diltiazem resulted in a 1.62fold increase for both C max and AUC 0-24 h . 12 Although the reduction of zanubrutinib exposures with the coadministration of a strong CYP3A inducer such as rifampin has been evaluated, the magnitude and extent of reduction with the co-administration of less potent CYP3A inducers is largely unknown.…”
mentioning
confidence: 99%