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Effects of aprepitant on cytochrome P450 3A4 activity using midazolam as a probe
Author(s) -
Majumdar Anup K.,
McCrea Jacqueline B.,
Panebianco Deborah L.,
Hesney Michael,
Dru James,
Constanzer Marvin,
Goldberg Michael R.,
Murphy Gail,
Gottesdiener Keith M.,
Lines Christopher R.,
Petty Kevin J.,
Blum Robert A.
Publication year - 2003
Publication title -
clinical pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.941
H-Index - 188
eISSN - 1532-6535
pISSN - 0009-9236
DOI - 10.1016/s0009-9236(03)00123-1
Subject(s) - aprepitant , cyp3a4 , pharmacology , midazolam , nk1 receptor antagonist , medicine , antagonist , antiemetic , pharmacokinetics , anesthesia , drug interaction , vomiting , cytochrome p450 , receptor , substance p , metabolism , neuropeptide , sedation
Background Aprepitant is a neurokinin 1 receptor antagonist that enhances prevention of chemotherapy‐induced nausea and vomiting when added to conventional therapy with a corticosteroid and a 5‐hydroxytryptamine 3 (5‐HT 3 ) antagonist. Because aprepitant may be used with a variety of chemotherapeutic agents and ancillary support drugs, which may be substrates of cytochrome P450 (CYP) 3A4, assessment of the potential of this drug to inhibit CYP3A4 activity in vivo is important. The effect of aprepitant on in vivo CYP3A4 activity in humans with oral midazolam used as a sensitive probe of CYP3A4 activity was evaluated in this study. Methods In this open‐label, randomized, single‐period study, 16 healthy male subjects were enrolled. Subjects received one of two oral aprepitant regimens for 5 days (8 subjects per regimen): (1) 125 mg aprepitant on day 1 and then 80 mg/d on days 2 to 5 or (2) 40 mg aprepitant on day 1 and then 25 mg/d on days 2 to 5. All subjects also received a single oral dose of midazolam, 2 mg, at prestudy (3 to 7 days before aprepitant treatment) and on days 1 and 5 (1 hour after aprepitant administration). Results Coadministration of midazolam and 125/80 mg aprepitant increased the midazolam area under the plasma concentration–time curve by 2.3‐fold on day 1 ( P < .01) and by 3.3‐fold on day 5 ( P < .01), as compared with midazolam alone (prestudy). The 125/80‐mg regimen of aprepitant also increased the midazolam maximum observed concentration by 1.5‐fold on day 1 ( P < .05) and by 1.9‐fold on day 5 ( P < .01). The midazolam half‐life values increased from 1.7 hours (prestudy) to 3.3 hours on both day 1 and day 5. Coadministration of 40/25 mg aprepitant and midazolam did not result in significant changes in the midazolam area under the plasma concentration–time curve, maximum observed concentration, and half‐life at either day 1 or day 5. Conclusions The 5‐day 125/80‐mg regimen of aprepitant produced moderate inhibition of CYP3A4 activity in humans, as measured with the use of midazolam as a probe drug. Clinical Pharmacology & Therapeutics (2003) 74 , 150–156; doi: 10.1016/S0009‐9236(03)00123‐1