Lack of a Clinically Significant Drug-Drug Interaction in Healthy Volunteers Between the Hepatitis C Virus Protease Inhibitor Boceprevir and the HIV Integrase Inhibitor Raltegravir

被引:21
作者
de Kanter, Clara T. M. M. [1 ,2 ]
Blonk, Maren I. [1 ,2 ]
Colbers, Angela P. H. [1 ,2 ]
Schouwenberg, Bas J. J. W. [3 ]
Burger, David M. [1 ,2 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Pharm, NL-6525 ED Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Nijmegen Inst Infect Inflammat & Immun, NL-6525 ED Nijmegen, Netherlands
[3] Radboud Univ Nijmegen, Med Ctr, Dept Pharmacol & Toxicol, NL-6525 ED Nijmegen, Netherlands
关键词
drug interactions; pharmacokinetics; hepatitis C; HIV; PHARMACOKINETICS; PHARMACOLOGY; TELAPREVIR; INFECTION; PROGRAM;
D O I
10.1093/cid/cis824
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Patients coinfected with human immunodeficiency virus (HIV) and hepatitis C virus (HCV) are likely to use both HIV and HCV treatment. Drug-drug interactions have been demonstrated between boceprevir, an HCV protease inhibitor, and frequently prescribed antiretroviral drugs, such as efavirenz and boosted HIV protease inhibitors. Concomitant administration of boceprevir with these drugs should be avoided. This study was designed to investigate the absence of a drug-drug interaction between boceprevir and raltegravir, an HIV integrase inhibitor. Methods. This was an open-label, randomized, 2-period, crossover phase 1 trial in 24 healthy volunteers. All subjects were randomly assigned to receive boceprevir 800 mg every 8 hours for 9 days plus a single dose of raltegravir 400 mg on day 10 followed by a washout period and a single dose of raltegravir 400 mg on day 38, or the same medication in reverse order. Blood samples for pharmacokinetics were collected and pharmacokinetic parameters were calculated. Results. The geometric mean (GM) of raltegravir area under the concentration-time curve (AUC) (0-12h) and maximum plasma concentration (C-max) for raltegravir + boceprevir vs raltegravir alone were 4.27 (95% confidence interval [CI], 3.22-5.66) vs 4.04 (95% CI, 3.09-5.28) mg * hour/L and 1.06 (95% CI, .76-1.49) vs 0.93 (95% CI, .70-1.23) mg/L, respectively. GM ratio estimates of raltegravir AUC(0-12h) and C-max for raltegravir + boceprevir vs raltegravir alone were 1.04 (90% CI, .88-1.22) and 1.11 (90% CI, .91-1.36), respectively. The GM of boceprevir AUC(0-8h), C-max, and C-8h were 5.45 (95% CI, 5.11-5.81) mg * hour/L, 1.88 (95% CI, 1.72-2.06) mg/L, and 0.09 (95% CI, .07-.11) mg/L, respectively. These data are comparable to those from historical controls. Conclusions. Due to the absence of a clinically significant drug interaction, raltegravir can be recommended for combined HIV/HCV treatment including boceprevir.
引用
收藏
页码:300 / 306
页数:7
相关论文
共 26 条
[1]  
[Anonymous], 19 C RETR OPP INF SE
[2]   The International Interlaboratory Quality Control Program for Measurement of Antiretroviral Drugs in Plasma: A Global Proficiency Testing Program [J].
Burger, David ;
Teulen, Marga ;
Eerland, Jaco ;
Harteveld, Anneke ;
Aarnoutse, Rob ;
Touw, Daan .
THERAPEUTIC DRUG MONITORING, 2011, 33 (02) :239-243
[3]   Raltegravir: a review of its pharmacokinetics, pharmacology and clinical studies [J].
Burger, David M. .
EXPERT OPINION ON DRUG METABOLISM & TOXICOLOGY, 2010, 6 (09) :1151-1160
[4]  
Burger David M, 2009, Eur J Med Res, V14 Suppl 3, P17
[5]  
Department of Health and Human Services. Panel on Antiretroviral Guidelines for Adults and Adolescents, 2012, GUID US ANT AG HIV 1
[6]  
European Medicines Agency, INC SUMM PROD CHAR
[7]  
European Medicines Agency, VICTR SUMM PROD CHAR
[8]  
FDA, INC PRESCR INF
[9]  
FDA, VICTR PRESCR INF
[10]  
FDA, Guidance for Industry: Statistical Approaches to Establishing Bioequivalence