Adding Maraviroc to the HAART Regimen of Well Controlled HIV-infected Patients

This is a prospective, open-label, non-controlled, non-randomized, single center study of the effect of adding the antiretroviral Maraviroc to the antiretroviral treatment regimen (HAART)of patients who have achieved a sustained virologic response to HAART but have had a sub-adequate immunologic response to treatment. Patients who have had a full virologic response (as defined by HIV-1 viral loads of < 48 copies/mL) for 12 months or more are defined as having a sub-adequate immunologic response if their CD4 lymphocyte count has not gone above 500.

This pilot study will contain up to 30 patients who will be followed over a period of 12 months starting from the date of enrollment and addition of maraviroc to their current highly active antiretroviral therapy regimen. The main outcome to be followed is the CD4 lymphocyte counts at baseline and after 12 months of treatment with the addition of maraviroc.

Inclusion criteria

• HIV-1 positive.
• Receiving highly active antiretroviral therapy (HAART).
• HIV-1 viral load of < 48 copies for 12 months or more.
• CD4 lymphocyte count that has not gone above 500. -

Exclusion criteria

• Severe hepatic impairment (cirrhosis) or active Hepatitis C with liver transaminases > 5 times normal.
• Severe renal impairment (creatinine clearance < 30 ml/min) or end-stage renal disease (ESRD) who are taking potent CYP3A4 inhibitors or inducers.
• Receiving certain necessary medications that have the potential for serious drug-drug interactions with maraviroc. -