Etravirine

被引:19
作者
Deeks, Emma D. [1 ]
Keating, Gillian M.
机构
[1] Wolters Kluwer Hlth I Adis, Auckland, New Zealand
关键词
D O I
10.2165/0003495-200868160-00007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Etravirine is a next-generation non-nucleoside reverse transcriptase inhibitor (NNRTI) that demonstrates potent in vitro activity against wild-type strains of HIV type I (HIV-1), as well as against numerous strains resistant to available NNRTIs. Furthermore, the potential for resistance to etravirine developing appears to be lower than for first-generation NNRTIs. In treatment-experienced patients infected with HIV-1 with NNRTI resistance, HIV-1 RNA levels of <50 copies/mL (primary endpoint) and <400 copies/mL were achieved by a significantly greater proportion of patients receiving etravirine 200 mg twice daily plus background therapy (BT) than placebo plus BT, according to the planned pooled and individual 24-week analyses of two large, well designed, continuing phase Ill trials (DUET-1 and DUET-2). In the pooled 24-week analysis, patients receiving etravirine plus BT achieved a significantly greater mean reduction in viral load from baseline and a significantly greater mean increase in CD4+ cell counts from baseline than patients receiving placebo plus BT. The pooled and individual findings of the DUET studies at 48 weeks indicate that the efficacy of etravirine is maintained with regard to these endpoints. In the DUET studies, etravirine was generally well tolerated in treatment-experienced patients infected with HIV-1, with a tolerability profile generally similar to that of placebo. Adverse events were mostly of mild or moderate severity.
引用
收藏
页码:2357 / 2372
页数:16
相关论文
共 68 条
[1]  
ANDERSON MS, 2007, 4 INT AIDS SOC C HIV
[2]   TMC125, a novel next-generation nonnucleoside reverse transcriptase inhibitor active against nonnucleoside reverse transcriptase inhibitor-resistant human immunodeficiency virus type 1 [J].
Andries, K ;
Azijn, H ;
Thielemans, T ;
Ludovici, D ;
Kukla, M ;
Heeres, J ;
Janssen, P ;
De Corte, B ;
Vingerhoets, J ;
Pauwels, R ;
de Béthune, MP .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (12) :4680-4686
[3]   Modulation of human immunodeficiency virus type 1 synergistic inhibition by reverse transcriptase mutations [J].
Basavapathruni, Aravind ;
Vingerhoets, Johan ;
de Bethune, Marie-Pierre ;
Chung, Raymond ;
Bailey, Christopher M. ;
Kim, Jiae ;
Anderson, Karen S. .
BIOCHEMISTRY, 2006, 45 (23) :7334-7340
[4]   Pharmacokinetics and antiretroviral response to darunavir/ritonavir and etravirine combination in patients with high-level viral resistance [J].
Boffito, Marta ;
Winston, Alan ;
Jackson, Akil ;
Fletcher, Carl ;
Pozniak, Anton ;
Nelson, Mark ;
Moyle, Graerne ;
Tolowinska, Izabela ;
Hoetelmans, Richard ;
Miralles, Diego ;
Gazzard, Brian .
AIDS, 2007, 21 (11) :1449-1455
[5]  
CAMPBELL T, 2007, HEP DART C DEC 9 13
[6]  
Clavel F, 2004, NEW ENGL J MED, V350, P1023, DOI 10.1056/NEJM2ra025195
[7]  
COHEN C, 2006, 16 INT AIDS C AUG 13
[8]   Roles of conformational and positional adaptability in structure-based design of TMC125-R165335 (etravirine) and related non-nucleoside reverse transcriptase inhibitors that are highly potent and effective against wild-type and drug-resistant HIV-1 variants [J].
Das, K ;
Clark, AD ;
Lewi, PJ ;
Heeres, J ;
de Jonge, MR ;
Koymans, LMH ;
Vinkers, HM ;
Daeyaert, F ;
Ludovici, DW ;
Kukla, MJ ;
De Corte, B ;
Kavash, RW ;
Ho, CY ;
Ye, H ;
Lichtenstein, MA ;
Andries, K ;
Pauwels, R ;
de Béthune, MP ;
Boyer, PL ;
Clark, P ;
Hughes, SH ;
Janssen, PAJ ;
Arnold, E .
JOURNAL OF MEDICINAL CHEMISTRY, 2004, 47 (10) :2550-2560
[9]  
DAVIS J, 2007, 11 EUR AIDS C OCT 24
[10]   Resistance profile and cross-resistance of HIV-1 among patients failing a non-nucleoside reverse transcriptase inhibitor-containing regimen [J].
Delaugerre, C ;
Rohban, R ;
Simon, A ;
Mouroux, M ;
Tricot, C ;
Agher, R ;
Huraux, JM ;
Katlama, C ;
Calvez, V .
JOURNAL OF MEDICAL VIROLOGY, 2001, 65 (03) :445-448