Efavirenz: shifting the HAART paradigm in adult HIV-1 infection
- PMID: 15992093
- DOI: 10.1517/13543784.8.4.473
Efavirenz: shifting the HAART paradigm in adult HIV-1 infection
Abstract
Efavirenz (DMP-266, Sustiva, Stocrin) is a member of the non-nucleoside class of HIV-1 reverse transcriptase inhibitors. It has demonstrated potent antiretroviral activity in treatment-naïve patients in combination with two nucleoside analogues or with a protease inhibitor. In nucleoside analogue-experienced patients, best activity has been seen with two nucleosides plus a protease inhibitor. An open-label comparison versus indinavir plus two nucleoside analogues in predominantly treatment-naïve patients, demonstrated that the efavirenz-based triple therapy provides at least similar antiviral effects, and possibly stronger effects, over 48 weeks. Furthermore, fewer patients discontinued efavirenz-based triple therapy than indinavir-based therapy because of adverse events. Side-effects associated with efavirenz include a maculopapular rash and central nervous system (CNS) disturbances (dizziness, vivid dreams, poor concentration, sleep disturbances) which generally occur, and resolve, within the first weeks of therapy. Efavirenz will be used as a combination agent with other antiretrovirals where therapy for HIV infection is indicated.
Similar articles
-
The emerging roles of non-nucleoside reverse transcriptase inhibitors in antiretroviral therapy.Drugs. 2001;61(1):19-26. doi: 10.2165/00003495-200161010-00003. Drugs. 2001. PMID: 11217868 Review.
-
Efavirenz: a pharmacoeconomic review of its use in HIV infection.Pharmacoeconomics. 2001;19(4):421-36. doi: 10.2165/00019053-200119040-00009. Pharmacoeconomics. 2001. PMID: 11383758 Review.
-
Efavirenz plus zidovudine and lamivudine, efavirenz plus indinavir, and indinavir plus zidovudine and lamivudine in the treatment of HIV-1 infection in adults. Study 006 Team.N Engl J Med. 1999 Dec 16;341(25):1865-73. doi: 10.1056/NEJM199912163412501. N Engl J Med. 1999. PMID: 10601505 Clinical Trial.
-
Efavirenz DuPont Pharmaceuticals Co.IDrugs. 1998 Oct;1(6):700-11. IDrugs. 1998. PMID: 18465625
-
Rilpivirine versus efavirenz with two background nucleoside or nucleotide reverse transcriptase inhibitors in treatment-naive adults infected with HIV-1 (THRIVE): a phase 3, randomised, non-inferiority trial.Lancet. 2011 Jul 16;378(9787):229-37. doi: 10.1016/S0140-6736(11)60983-5. Lancet. 2011. PMID: 21763935 Clinical Trial.
Cited by
-
An Expanded Analysis of Pharmacogenetics Determinants of Efavirenz Response that Includes 3'-UTR Single Nucleotide Polymorphisms among Black South African HIV/AIDS Patients.Front Genet. 2016 Jan 7;6:356. doi: 10.3389/fgene.2015.00356. eCollection 2015. Front Genet. 2016. PMID: 26779253 Free PMC article.
-
The emerging roles of non-nucleoside reverse transcriptase inhibitors in antiretroviral therapy.Drugs. 2001;61(1):19-26. doi: 10.2165/00003495-200161010-00003. Drugs. 2001. PMID: 11217868 Review.
-
Efavirenz: a pharmacoeconomic review of its use in HIV infection.Pharmacoeconomics. 2001;19(4):421-36. doi: 10.2165/00019053-200119040-00009. Pharmacoeconomics. 2001. PMID: 11383758 Review.
-
Dendritic spine injury induced by the 8-hydroxy metabolite of efavirenz.J Pharmacol Exp Ther. 2012 Dec;343(3):696-703. doi: 10.1124/jpet.112.195701. Epub 2012 Sep 13. J Pharmacol Exp Ther. 2012. PMID: 22984227 Free PMC article.
-
DPC 681 and DPC 684: potent, selective inhibitors of human immunodeficiency virus protease active against clinically relevant mutant variants.Antimicrob Agents Chemother. 2001 Nov;45(11):3021-8. doi: 10.1128/AAC.45.11.3021-3028.2001. Antimicrob Agents Chemother. 2001. PMID: 11600351 Free PMC article.
LinkOut - more resources
Full Text Sources