Lack of Effect of Brivanib on the Pharmacokinetics of Midazolam, a CYP3A4 Substrate, Administered Intravenously and Orally in Healthy Participants

التفاصيل البيبلوغرافية
العنوان: Lack of Effect of Brivanib on the Pharmacokinetics of Midazolam, a CYP3A4 Substrate, Administered Intravenously and Orally in Healthy Participants
المؤلفون: Pamela L. Clemens, Shariq Syed, Arindam Dhar, Ian Walters, Eric Masson, Deanne Lathers, Georgia Kollia
المصدر: The Journal of Clinical Pharmacology. 52:914-921
بيانات النشر: Wiley, 2012.
سنة النشر: 2012
مصطلحات موضوعية: Adult, Male, Patient Dropouts, genetic structures, Midazolam, Administration, Oral, Antineoplastic Agents, Pharmacology, chemistry.chemical_compound, Pharmacokinetics, Oral administration, medicine, Cytochrome P-450 CYP3A, Humans, Drug Interactions, Prodrugs, Pharmacology (medical), Alanine, Cross-Over Studies, Dose-Response Relationship, Drug, CYP3A4, Triazines, business.industry, Middle Aged, Prodrug, Crossover study, Fibroblast Growth Factors, Intestines, Receptors, Vascular Endothelial Growth Factor, Brivanib alaninate, Liver, Tolerability, chemistry, Injections, Intravenous, Cytochrome P-450 CYP3A Inhibitors, Female, Metabolic Detoxication, Phase I, business, Half-Life, medicine.drug
الوصف: Brivanib alaninate is the orally available prodrug of brivanib, a dual inhibitor of fibroblast growth factor and vascular endothelial growth factor signaling pathways that is under therapeutic investigation for various malignancies. Brivanib alaninate inhibits CYP3A4 in vitro, and thus there is potential for drug-drug interaction with CYP3A4 substrates, such as midazolam. The present study evaluated pharmacokinetic parameters and safety/tolerability upon coadministration of brivanib alaninate and midazolam. Healthy participants received intravenous (IV) or oral midazolam with and without oral brivanib alaninate. Blood samples for pharmacokinetic analysis were collected up to 12 hours after midazolam and up to 48 hours after brivanib alaninate. Twenty-four participants were administered study drugs; 21 completed the trial. No clinically relevant effect of brivanib alaninate on the overall exposure to midazolam following IV or oral administration was observed. Orally administered brivanib alaninate was generally well tolerated in the presence of IV or oral midazolam. The lack of a pharmacokinetic interaction between brivanib and midazolam indicates that brivanib alaninate does not influence either intestinal or hepatic CYP3A4 and confirms that brivanib alaninate may be safely coadministered with midazolam and other CYP3A4 substrates.
تدمد: 0091-2700
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcaebc4588223e4e66de77c03ed910fcTest
https://doi.org/10.1177/0091270011407495Test
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....dcaebc4588223e4e66de77c03ed910fc
قاعدة البيانات: OpenAIRE
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