Article ID Journal Published Year Pages File Type
3332604 HIV & AIDS Review 2007 5 Pages PDF
Abstract
Retroviral enzyme integrase is absolutely indispensable to HIV-1 replication by catalysing proviral HIV DNA integration into host genome. Its inhibition becomes a new therapeutic target for antiretroviral therapy. For ten last years many integrase inhibitors molecules have been discovered. The most promising are raltegravir (RAL) and elvitegravir (EVG). Raltegravir (Isentress®) is the first oral integrase inhibitor which received FDA and EMEA approval, respectively in October and December 2007. This ARV drug is indicated in treatment-experienced adult HIV-1 infected patients with multidrug resistances, who have already been exposed to simply three ARV classes.
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