Lack of a clinically significant drug-drug interaction in healthy volunteers between the HCV protease inhibitor boceprevir and the proton pump inhibitor omeprazole
Author(s) -
Clara T. M. M. de Kanter,
Angela Colbers,
Maren I. Blonk,
C.P.W.G.M. Verwey-van Wissen,
B.J.J.W. Schouwenberg,
Joost P.H. Drenth,
David M. Burger
Publication year - 2013
Publication title -
journal of antimicrobial chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.124
H-Index - 194
eISSN - 1460-2091
pISSN - 0305-7453
DOI - 10.1093/jac/dkt032
Subject(s) - boceprevir , omeprazole , medicine , pharmacokinetics , cmax , pharmacology , proton pump inhibitor , telaprevir , gastroenterology , hepatitis c virus , immunology , virus , ribavirin
Proton pump inhibitors (PPIs) can limit the solubility of concomitant drugs, which can lead to decreased absorption and exposure. Reduced efficacy can be a consequence and in the case of an antimicrobial agent this may contribute to development of resistance. Patients chronically infected with the hepatitis C virus can be treated with a boceprevir-containing regimen and it is relevant to know if interactions between PPIs and boceprevir exist. This study was designed to investigate the influence of a frequently used PPI, omeprazole, on the pharmacokinetics of boceprevir and vice versa.
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