Drug Interactions with New and Investigational Antiretrovirals

被引:67
作者
Brown, Kevin C. [1 ]
Paul, Sunita [1 ]
Kashuba, Angela D. M. [1 ]
机构
[1] Univ N Carolina, Sch Pharm, Ctr AIDS Res Clin Pharmacol & Analyt Chem Core, Chapel Hill, NC 27599 USA
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; NEGATIVE HEALTHY-VOLUNTEERS; HIGH GENETIC BARRIER; PHARMACOKINETIC INTERACTION; ANTIVIRAL ACTIVITY; CCR5; ANTAGONIST; CLINICAL PHARMACOKINETICS; PROTEASE INHIBITOR; TREATMENT-NAIVE; IN-VITRO;
D O I
10.2165/00003088-200948040-00001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
More than 20 individual and fixed-dose combinations of antiretrovirals are approved for the treatment of human immunodeficiency virus (HIV) infection. However, owing to the ongoing limitations of drug resistance and adverse effects, new treatment options are still required. A number of promising new agents in existing or new drug classes are in development or have recently been approved by the US FDA. Since these agents will be used in combination with other new and existing antiretrovirals, understanding the potential for drug interactions between these compounds is critical to their appropriate use. This article summarizes the drug interaction potential of new and investigational protease inhibitors (darunavir), non-nucleoside reverse transcriptase inhibitors (etravirine and rilpivirine), chemokine receptor antagonists (maraviroc, vicriviroc and INCB 9471), integrase inhibitors (raltegravir and elvitegravir) and maturation inhibitors (bevirimat).
引用
收藏
页码:211 / 241
页数:31
相关论文
共 143 条
  • [1] ABEL S, 2007, 8 INT WORKSH PHARM H
  • [2] ABEL S, 2005, 10 EUR AIDS C NOV 17
  • [3] ABEL S, 2003, 10 C RETR OPP INF FE
  • [4] ABEL S, 2004, 5 INT WORKSH CLIN PH
  • [5] Effect of maraviroc on the pharmacokinetics of midazolam, lamivudine/zidovudine, and ethinyloestradiol/levonorgestrel in healthy volunteers
    Abel, Samantha
    Russell, Deborah
    Whitlock, Lyndsey A.
    Ridgway, Caroline E.
    Muirhead, Gary J.
    [J]. BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2008, 65 : 19 - 26
  • [6] Effects of CYP3A4 inhibitors on the pharmacokinetics of maraviroc in healthy volunteers
    Abel, Samantha
    Russell, Deborah
    Taylor-Worth, Richard J.
    Ridgway, Caroline E.
    Muirhead, Gary J.
    [J]. BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2008, 65 : 27 - 37
  • [7] Effects of CYP3A4 inducers with and without CYP3A4 inhibitors on the pharmacokinetics of maraviroc in healthy volunteers
    Abel, Samantha
    Jenkins, Timothy M.
    Whitlock, Lyndsey A.
    Ridgway, Caroline E.
    Muirhead, Gary J.
    [J]. BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2008, 65 : 38 - 46
  • [8] Assessment of the pharmacokinetics, safety and tolerability of maraviroc, a novel CCR5 antagonist, in healthy volunteers
    Abel, Samantha
    van der Ryst, Elna
    Rosario, Maria C.
    Ridgway, Caroline E.
    Medhurst, Christine G.
    Taylor-Worth, Richard J.
    Muirhead, Gary J.
    [J]. BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2008, 65 : 5 - 18
  • [9] Assessment of the absorption, metabolism and absolute bioavailability of maraviroc in healthy male subjects
    Abel, Samantha
    Russell, Deborah
    Whitlock, Lyndsey A.
    Ridgway, Caroline E.
    Nedderman, Angus N. R.
    Walker, Donald K.
    [J]. BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2008, 65 : 60 - 67
  • [10] Andersen A, 2007, EUR J PUBLIC HEALTH, V17, P20