In vitro cytochrome P450 inhibition and induction
“At in vitro concentrations of 3 μmol/L, which are much higher than those anticipated to be clinically efficacious, azetukalner did not cause direct inhibition of CYP1A2, CYP2C9, CYP2C19, CYP2D6, and CYP3A4, nor did it cause time-dependent inhibition” (opens the source at this quote in a new tab)
“Likewise, no clinically meaningful induction of the pregnane X nuclear receptor (PXR), which is associated with CYP3A4 expression levels, was observed at azetukalner concentrations of 0.1–1 μmol/L” (opens the source at this quote in a new tab)
Low potential for drug interactions in clinical use
No dose adjustment of concomitant antiseizure medications
Effect on hormonal contraceptives
No evidence found.