Literature DB >> 23420097

Does once-daily etravirine have a role in the management of HIV-1 infection?

Ian R McNicholl1.   

Abstract

When individualizing therapy for HIV-positive patients and for those in whom the 'preferred regimens' of the US Department of Health and Human Services HIV treatment guidelines are not appropriate, a once-daily non-nucleoside with a fixed-dose combination of two nucleosides may be considered in patients who are adherence challenged, intolerant to other regimens but with no viral resistance, or in those in whom the pill burden or actual pill size was too great to accept. Despite having a 30- to 40-h elimination half-life, etravirine was never considered for once-daily dosing during development due to an unacceptably high pill burden in phase II trials. However, a recently published study, SENSE, enrolled 157 HIV-positive patients in a multinational, randomized, placebo-controlled, double-blind trial that investigated 400 mg etravirine once daily with two nucleosides versus a comparator arm that included efavirenz and two nucleosides. The primary objective was to assess neuropsychiatric tolerability over the 48-week study period, with comparative efficacy as a secondary objective. Using the intent-to-treat time to loss of virologic response (ITT-TLOVR) analysis at 48 weeks, 76 % of patients receiving etravirine had an undetectable viral load of <50 copies/mL compared with 74 % of patients receiving efavirenz. This translates to a suppression rate difference of 1.6 % favouring etravirine (95 % CI -12.0-15.2) and met the non-inferiority criteria of a delta of -12 %. Baseline viral load was not observed to impact clinical response rates. Pharmacokinetically and clinically, studies indicate the efficacy and safety of utilizing once-daily etravirine in the treatment-naive population. While it is not appropriate for all patients, once-daily etravirine is best utilized for patients in whom caloric requirements, pill burden, pill size, potential adverse reactions, concomitant medications/drug interactions, psychosocial factors and patient preference preclude the use of a 'preferred' regimen. Etravirine dissolution in water allows for the flexibility of once-daily dosing with one fixed-dose combination tablet followed by an etravirine/water 'chaser'.

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Year:  2013        PMID: 23420097     DOI: 10.1007/s40265-013-0022-6

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   11.431


  12 in total

1.  Intracellular and plasma pharmacokinetics of 400 mg of etravirine once daily versus 200 mg of etravirine twice daily in HIV-infected patients.

Authors:  Alicia Gutiérrez-Valencia; Reyes Martin-Peña; Almudena Torres-Cornejo; Rosa Ruiz-Valderas; Juan R Castillo-Ferrando; Luis F López-Cortés
Journal:  J Antimicrob Chemother       Date:  2011-12-21       Impact factor: 5.790

2.  A phase IV, double-blind, multicentre, randomized, placebo-controlled, pilot study to assess the feasibility of switching individuals receiving efavirenz with continuing central nervous system adverse events to etravirine.

Authors:  Laura Waters; Martin Fisher; Alan Winston; Chris Higgs; Wendy Hadley; Lucy Garvey; Sundhiya Mandalia; Nicky Perry; Mackie Nicola; Mark Nelson
Journal:  AIDS       Date:  2011-01-02       Impact factor: 4.177

3.  Phase 2 double-blind, randomized trial of etravirine versus efavirenz in treatment-naive patients: 48-week results.

Authors:  Brian Gazzard; Claudine Duvivier; Christian Zagler; Antonella Castagna; Andrew Hill; Yvonne van Delft; Stephan Marks
Journal:  AIDS       Date:  2011-11-28       Impact factor: 4.177

4.  Effect of cobicistat on glomerular filtration rate in subjects with normal and impaired renal function.

Authors:  Polina German; Hui C Liu; Javier Szwarcberg; Mischa Hepner; Jessica Andrews; Brian P Kearney; Anita Mathias
Journal:  J Acquir Immune Defic Syndr       Date:  2012-09-01       Impact factor: 3.731

5.  Rilpivirine versus efavirenz with tenofovir and emtricitabine in treatment-naive adults infected with HIV-1 (ECHO): a phase 3 randomised double-blind active-controlled trial.

Authors:  Jean-Michel Molina; Pedro Cahn; Beatriz Grinsztejn; Adriano Lazzarin; Anthony Mills; Michael Saag; Khuanchai Supparatpinyo; Sharon Walmsley; Herta Crauwels; Laurence T Rimsky; Simon Vanveggel; Katia Boven
Journal:  Lancet       Date:  2011-07-16       Impact factor: 79.321

6.  TMC125, a novel next-generation nonnucleoside reverse transcriptase inhibitor active against nonnucleoside reverse transcriptase inhibitor-resistant human immunodeficiency virus type 1.

Authors:  Koen Andries; Hilde Azijn; Theo Thielemans; Donald Ludovici; Michael Kukla; Jan Heeres; Paul Janssen; Bart De Corte; Johan Vingerhoets; Rudi Pauwels; Marie-Pierre de Béthune
Journal:  Antimicrob Agents Chemother       Date:  2004-12       Impact factor: 5.191

7.  Pharmacokinetics of once-daily etravirine without and with once-daily darunavir/ritonavir in antiretroviral-naive HIV type-1-infected adults.

Authors:  Edwin DeJesus; Jacob P Lalezari; Olayemi O Osiyemi; Peter J Ruane; Robert Ryan; Thomas N Kakuda; James Witek
Journal:  Antivir Ther       Date:  2010

8.  Impact of reverse transcriptase resistance on the efficacy of TMC125 (etravirine) with two nucleoside reverse transcriptase inhibitors in protease inhibitor-naïve, nonnucleoside reverse transcriptase inhibitor-experienced patients: study TMC125-C227.

Authors:  K Ruxrungtham; R J Pedro; G H Latiff; F Conradie; P Domingo; S Lupo; W Pumpradit; J H Vingerhoets; M Peeters; I Peeters; T N Kakuda; G De Smedt; B Woodfall
Journal:  HIV Med       Date:  2008-09-14       Impact factor: 3.180

9.  Single- and multiple-dose pharmacokinetics of etravirine administered as two different formulations in HIV-1-infected patients.

Authors:  Thomas N Kakuda; Monika Schöller-Gyüre; Cassy Workman; Keikawus Arasteh; Anton L Pozniak; Goedele De Smedt; Greet Beets; Monika Peeters; Kati Vandermeulen; Brian J Woodfall; Richard M W Hoetelmans
Journal:  Antivir Ther       Date:  2008

Review 10.  Etravirine and rilpivirine: nonnucleoside reverse transcriptase inhibitors with activity against human immunodeficiency virus type 1 strains resistant to previous nonnucleoside agents.

Authors:  Patricia Pecora Fulco; Ian R McNicholl
Journal:  Pharmacotherapy       Date:  2009-03       Impact factor: 4.705

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