@article{oai:hama-med.repo.nii.ac.jp:00003792,
 author = {Katayama, Naoki and Odagiri, Keiichi and Hakamata, Akio and Kamiya, Chiaki and Uchida, Shinya and Tanaka, Shimako and Inui, Naoki and Namiki, Noriyuki and Tatsumi, Koichiro and Watanabe, Hiroshi},
 issue = {4},
 journal = {British Journal of Clinical Pharmacology},
 month = {Apr},
 note = {Aims: The strong cytochrome P450 (CYP) 2C8 inhibitor gemfibrozil has been demonstrated to increase the area under the plasma concentration-time curve from 0 to infinity (AUC0?∞) of ACT-333679, an active metabolite of selexipag, by 11-fold. Similarly as gemfibrozil, the CYP2C8 inhibitor clopidogrel also increases clopidogrel increased ACT-333679 concentration by 1.9-fold after a single loading dose (300 mg once daily) and 2.7-fold after repeated treatment with the maintenance dose (75 mg once daily) in Europeans. However, the effects of clopidogrel on the pharmacokinetics of selexipag and ACT-333679 have not been fully elucidated in Japanese population.
Methods: We investigated the effect of clopidogrel on the pharmacokinetics of selexipag and ACT-333679 in 14 healthy Japanese volunteers.
Results: The concomitant administration of clopidogrel with selexipag did not influence the maximum concentration (Cmax) and AUC0-∞ of selexipag, whereas it significantly increased AUC0-∞ of ACT-333679 by approximately 1.90-fold (90% confidence interval (CI) 1.69?2.14) without changing Cmax. When selexipag was administered 1 day after clopidogrel was discontinued, the increase in AUC0-∞ of ACT-333679 was 1.37-fold (90% CI 0.93?2.02), suggesting that although the inhibitory effect of clopidogrel on CYP2C8 was reduced, it persisted for at least 1 day after withdrawal.
Conclusion: Our results demonstrated the impact of clopidogrel on the pharmacokinetics of selexipag and its active metabolite and suggested that selexipag should be carefully prescribed with clopidogrel with dose adjustment or reducing the dosing frequency in Japanese clinical settings.},
 pages = {1903--1911},
 title = {Clinical evaluation of drug?drug interactions between the cytochrome P450 substrates selexipag and clopidogrel in Japanese volunteers},
 volume = {87},
 year = {2021}
}