Preferred antiretroviral drugs for the next decade of scale up
- PMID: 23010379
- PMCID: PMC3494169
- DOI: 10.7448/IAS.15.2.17986
Preferred antiretroviral drugs for the next decade of scale up
Abstract
Global commitments aim to provide antiretroviral therapy (ART) to 15 million people living with HIV by 2015, and recent studies have demonstrated the potential for widespread ART to prevent HIV transmission. Increasingly, countries are adapting their national guidelines to start ART earlier, for both clinical and preventive benefits. To maximize the benefits of ART in resource-limited settings, six key principles need to guide ART choice: simplicity, tolerability and safety, durability, universal applicability, affordability and heat stability. Currently available drugs, combined with those in late-stage clinical development, hold great promise to simplify treatment in the short term. Over the longer-term, newer technologies, such as long-acting formulations and nanotechnology, could radically alter the treatment paradigm. This commentary reviews recommendations made in an expert consultation on treatment scale up in resource-limited settings.
References
-
- United Nations General Assembly. Political declaration on HIV/AIDS: intensifying our efforts to eliminate HIV/AIDS – United Nations General Assembly Resolution 65/277; New York, United Nations. 2011.
-
- Progress report 2011. Global HIV/AIDS response Epidemic update and health sector progress towards universal access. WHO, UNICEF, UNAIDS. Geneva, Switzerland: December 2011.
-
- US Food and Drugs Administration. Antiretroviral drugs used in the treatment of HIV infection. 2012. Available from: http://www.fda.gov/ForConsumers/ByAudience/ForPatientAdvocates/HIVandAID....
-
- Lynch S, Ford N, van Cutsem G, Bygrave H, Janssens B, Decroo T. Getting HIV treatment to the most people. Science. 2012;337(6092):298–300. - PubMed
-
- Antiretroviral Sequencing Meeting Report. MSF. Geneva. 2011. Available from: http://www.msfaccess.org/content/antiretroviral-sequencing-meeting-report.
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