Efavirenz/emtricitabine/tenofovir disoproxil fumarate fixed-dose combination: first-line therapy for all?

被引:19
作者
Goicoechea, Miguel
Best, Brookie
机构
[1] Univ Calif San Diego, Sch Med, San Diego, CA 92103 USA
[2] Antiviral Res Ctr, San Diego, CA 92103 USA
[3] Univ Calif San Diego, Skaggs Sch Pharm & Pharmaceut Sci, San Diego, CA 92103 USA
关键词
efavirenz; emtricitabine; fixed-dose combination; HIV; tenofovir;
D O I
10.1517/14656566.8.3.371
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
ATRIPLA(TM) (Bristol-Myers Squibb and Gilead Sciences) is a complete regimen in a single, fixed-dose combination tablet that contains: efavirenz 600 mg, emtricitabine 200 mg and tenofovir disoproxil fumarate 300 mg. Current treatment guidelines recommend this triple combination for initial therapy because of its excellent potency, tolerability and favorable safety profile. individually, these agents have long half-lifes that allow for once-daily dosing and may provide a pharmacologic bridge for the occasional missed dose. Although several options for once-daily regimens are available, comparative clinical trials are still in progress. This article reviews relevant efficacy and safety data of efavirenz, emtricitabine and tenofovir disoproxil fumarate, compared with other once-daily agents or certain common alternate drugs presently used as initial therapy in treatment-naive patients.
引用
收藏
页码:371 / 382
页数:12
相关论文
共 86 条
[1]  
BARTLETT JA, 2004, 15 INT AIDS C BANGK
[2]   A randomized study of emtricitabine and lamivudine in stably suppressed patients with HIV [J].
Benson, CA ;
van der Horst, C ;
LaMarca, A ;
Haas, DW ;
McDonald, CK ;
Steinhart, CR ;
Rublein, J ;
Quinn, JB ;
Mondou, E ;
Rousseau, F .
AIDS, 2004, 18 (17) :2269-2276
[3]  
Bickel M, 2005, SCAND J INFECT DIS, V37, P520, DOI 10.1080/00365540410020901
[4]   Assessment of mitochondrial toxicity in human cells treated with tenofovir: Comparison with other nucleoside reverse transcriptase inhibitors [J].
Birkus, G ;
Hitchcock, MJM ;
Cihlar, T .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (03) :716-723
[5]   HIV-1 drug resistance in newly infected individuals [J].
Boden, D ;
Hurley, A ;
Zhang, LQ ;
Cao, YZ ;
Guo, Y ;
Jones, E ;
Tsay, J ;
Ip, J ;
Farthing, C ;
Limoli, K ;
Parkin, N ;
Markowitz, M .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 282 (12) :1135-1141
[6]  
BOYLE BA, 2005, 15 INT AIDS C BANGK
[7]   Adverse effects of reverse transcriptase inhibitors: mitochondrial toxicity as common pathway [J].
Brinkman, K ;
ter Hofstede, HJM ;
Burger, DM ;
Smeitinkt, JAM ;
Koopmans, PP .
AIDS, 1998, 12 (14) :1735-1744
[8]  
CASCADE Collaboration, 2000, LANCET, V355, P1158, DOI 10.1016/S0140-6736(00)02069-9
[9]   Neuropsychiatric complications of antiretroviral therapy [J].
Cespedes, Michelle S. ;
Aberg, Judith A. .
DRUG SAFETY, 2006, 29 (10) :865-874
[10]   Role of minority populations of human immunodeficiency virus type 1 in the evolution of viral resistance to protease inhibitors [J].
Charpentier, C ;
Dwyer, DE ;
Mammano, F ;
Lecossier, D ;
Clavel, F ;
Hance, AJ .
JOURNAL OF VIROLOGY, 2004, 78 (08) :4234-4247