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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/19665
Title: Potential for new antiretrovirals to address unmet needs in the management of HIV-1 infection
Authors: Graeme Moyle
Jose Gatell
Carlo Federico Perno
Winai Ratanasuwan
Mauro Schechter
Christos Tsoukas
Chelsea and Westminster Hospital
Universitat de Barcelona
Universita degli Studi di Roma La Sapienza
Mahidol University
Universidade Federal do Rio de Janeiro
McGill University
Keywords: Medicine
Issue Date: 1-Jun-2008
Citation: AIDS Patient Care and STDs. Vol.22, No.6 (2008), 459-471
Abstract: Despite the myriad advances in antiretroviral therapy since the original highly active antiretroviral therapy regimens were developed, there remain numerous important and pressing unmet needs that, if addressed, would substantially improve the quality of life and longevity of HIV-infected patients. The most achievable goals of antiretroviral (ARV) therapy in the near future are likely to be continued reduction in HIV-related morbidity and mortality; improved quality of life; and restoration and preservation of immune function: all of which are most effectively achieved through sustained suppression of HIV-1 RNA. The ability to achieve long-term viral load reduction will require new ARVs with few, manageable toxicities, and medications that are convenient to adhere to, with few drug interactions. This is particularly true for the large number of highly treatment-experienced patients in whom HIV has developed resistance to one or more ARVs. Development of therapies that allow convenient dosing schedules, that do not necessitate strict adherence to meal-related timing restrictions, and that remain active in the face of resistance mutations is paramount, and remains a significant unmet need. Of the large number of ARVs currently in development, this article focuses on three agents recently approved that have shown particular promise in addressing some of these unmet needs: the novel non-nucleoside reverse transcriptase inhibitor etravirine; the CCR5 antagonist maraviroc; and the integrase inhibitor raltegravir. © 2008 Mary Ann Liebert, Inc.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=48049107573&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/19665
ISSN: 10872914
Appears in Collections:Scopus 2006-2010

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