Christoph Boesecke¹ and Linda Gelgor^1,2

¹National Centre in HIV Epidemiology and Clinical Research, University of New South Wales, Sydney, Australia. ²St. Vincent’s Centre for Applied Medical Research, University of New South Wales, Sydney, Australia.  

Abstract  

Raltegravir is the first antiretroviral drug in the class of integrase inhibitors approved for the treatment of human immunodeficiency virus type 1 (HIV-1) in combination with other antiretroviral agents in treatment-experienced adults with evidence of ongoing viral replication and resistance to multiple antiretroviral drugs. Since raltegravir has a different mechanism of action to the currently licensed antiretroviral agents, it is a welcome addition in the treatment of HIV-1. Results from clinical studies to date indicate that raltegravir exhibits potent antiviral activity particularly against HIV-1 strains which exhibit resistance to other classes of antiretroviral drugs. It is well tolerated and has a favorable safety profile. Long-term follow-up data on its resistance profile and on potential interactions with other antiretroviral as well as concomitant medications will ultimately define its future role in the treatment of HIV-1 infection. This review briefly describes the mechanism of action of raltegravir and its pharmacokinetic profile, summarizes efficacy and safety data from recent clinical trials and implications for the use in treatment-naïve as well as treatment-experienced patients, depicts raltegravir’s emerging resistance profile, and highlights potential drug-drug interactions.