LAUSR

Amenamevir (formerly ASP2151) is a helicase‐primase inhibitor being developed for the treatment of herpesvirus infection. Amenamevir is both a substrate and inducer of cytochrome P450 (CYP) 3A4. Three studies were done in healthy volunteers to investigate potential CYP3A pharmacokinetic interactions with the following drugs: (1) Midazolam (probe substrate for CYP3A): After 10 days’ pretreatment with amenamevir 400 mg daily, geometric mean maximum concentration of drug in blood plasma (Cmax) and area under the plasma drug concentration‐time curve from time zero to infinity (AUC0‐∞) of midazolam 7.5 mg were about 68% and 51%, respectively, of those after midazolam alone. (2) Cyclosporine (substrate and inhibitor of CYP3A): After 5 days’ pretreatment with cyclosporine 100 mg twice daily, geometric mean Cmax of amenamevir after 400‐mg and 1200‐mg single doses was, respectively, about 66% and 69%, and AUC0‐∞ about 82% and 79%, of those after amenamevir alone. (3) Ritonavir (inhibitor of CYP3A): When given with single doses of ritonavir 600 mg, geometric mean Cmax of amenamevir after 400‐mg and 1200‐mg single doses was, respectively, about 1.4 and 1.6 times higher, and geometric mean AUC0‐∞ about 2.6 and 3.3 times higher, than after amenamevir alone. Amenamevir has the potential to be involved in CYP3A‐mediated pharmacokinetic interactions in clinical practice.