New antiretroviral drugs in clinical use

被引:10
作者
Pimpanada Chearskul
Chokechai Rongkavilit
Hossam Al-Tatari
Basim Asmar
机构
[1] Wayne State University,Carman and Ann Adams Department of Pediatrics
[2] School of Medicine,Division of Infectious Diseases
[3] Children's Hospital of Michigan,undefined
关键词
Antiretroviral drugs; HIV; Children;
D O I
10.1007/BF02825828
中图分类号
学科分类号
摘要
The advent of combination antiretroviral therapy for the treatment of human immunodeficiency virus (HIV) infection has dramatically changed the prognosis and quality of life of HIV-infected adults and children. To date, there are 21 antiretroviral agents available with only 11 agents being approved for the use in young children less than 6 years of age. The currently available antiretroviral agents belong to four different classes; nucleoside/nucleotide reverse transcriptase inhibitors (NRTI, NtRTI), non-nucleoside reverse transcriptase inhibitors (NNRTI), protease inhibitors (PI), and a new class of fusion inhibitors (FI). It is recommended that the treatment regimen should be a combination of at least 3 drugs from different drug classes as this has been shown to slow disease progression, improve survival, and result in better virologic and immunologic responses. Treatment with antiretroviral agents is frequently complicated by the issues of adherence, tolerability, long term toxicity and drug resistance. Many efforts have been made to develop new antiretroviral agents with greater potency, higher tolerability profiles and better convenience. Some new agents are also effective against drug-resistant strains of HIV. Since 2001, there were 7 new antiretroviral agents and 2 fixed-dose multidrug formulations being approved for the treatment of HIV infection, most are approved only for use in adults. In this article, we will review new antiretroviral agents including emtricitabine, tenofovir disoproxil fumarate, atazanavir, fosamprenavir, tipranavir and enfuvirtide. Pediatric information on these drugs will be provided when available.
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页码:335 / 341
页数:6
相关论文
共 247 条
[1]
Modrzejewski KA(2004)Emtricitabine: a once-daily nucleoside reverse transcriptase inhibitor Ann Pharmacother 38 1006-1014
[2]
Herman RA(1992)Selective inhibition of human immunodeficiency viruses by racemates and enantiomers of cis-5-fluoro-1-[2-(hydroxymethyl)-1,3-oxathiolan-5-yl]cytosine Antimicrob Agents Chemother 36 2423-2431
[3]
Schinazi RF(2005)Emtricitabine: a review of its use in the management of HIV infection Drugs 65 1427-1448
[4]
McMillan A(2004)Efficacy and safety of emtricitabine vs stavudine in combination therapy in antiretroviral-naive patients: a randomized trial Jama 292 180-189
[5]
Cannon D(2000)Once-daily combination therapy with emtricitabine, didanosine, and efavirenz in human immunodeficiency virus-infected patients J Infect Dis 182 599-602
[6]
Mathis R(2004)A randomized study of emtricitabine and lamivudine in stably suppressed patients with HIV Aids 18 2269-2276
[7]
Lloyd RM(2005)Simplification therapy with once-daily emtricitabine, didanosine, and efavirenz in HIV-1-infected adults with viral suppression receiving a protease inhibitor-based regimen: a randomized trial J Infect Dis 191 830-839
[8]
Peck A(2002)Dose range study of pharmacokinetics, safety, and preliminary antiviral activity of emtricitabine in adults with hepatitis B virus infection Antimicrob Agents Chemother 46 1734-1740
[9]
Frampton JE(2004)Pharmacokinetics and safety of single oral doses of emtricitabine in human immunodeficiency virus-infected children Antimicrob Agents Chemother 48 183-191
[10]
Perry CM(1999)The pharmacokinetics of lamivudine phosphorylation in peripheral blood mononuclear cells from patients infected with HIV-1 Aids 13 2239-2250