Since B-cell signaling is central for malignant B cells survival, improved nib-mediated BTK inhibition reduces malignant B-cell proliferation and survival.
Both
Neither
Ibrutinib pharmacokinetics/pharmacodynamics:
Ibrutinib administration with food doubles absorption compared to administration on an empty stomach.
Ibrutinib is metabolized by the cytochrome P450 drug metabolizing system, utilizing mainly CYP3A and to a lesser extent CYP2D6 isoforms.
Both
Neither
Ibrutinib metabolism:
Excretion is mainly via the feces
Hepatic functional impairment would tend to increase patient exposure to a Ibrutinib.
Both
Neither
Ibrutinib resistance is mainly due to Pgp (P-glycoprotein 1) a.k.a. multidrug-resistant protein 1.