Maraviroc Abacavir STudy - Effect on Endothelial Recovery

• Status: Unknown status
• Trial end date: 2014-10-01
• Target enrollment: 0
• Participant gender: All

Summary

HIV infected patients treated with abacavir might have a higher risk for the occurrence of cardiovascular events. At time of writing of this protocol the underlying mechanism is not yet elucidated, however some studies find impaired endothelial function and elevated markers of chronic inflammation in these patients,suggesting a higher lever of chronic inflammation. Recently maraviroc (Celsentri®), a CCR5-receptor antagonist, became available for treatment of patients infected with HIV-1.

Improvement of endothelial function may be a potential beneficial side effect of treatment with maraviroc, due to the potential reduction of immune activation and chronic inflammation as a result of blocking the CCR5-coreceptor. Moreover, treatment intensification of HAART with maraviroc in patients with suppressed plasma HIV_RNA may decrease plasma HIVRNA below the cut-off of 50 copies/ml as well.

The investigators hypothesize that maraviroc intensification therapy in patients on an abacavir-containing regimen will improve endothelial function.

The objectives of this study are: First, to assess the effect of addition of maraviroc to an abacavir-containing regimen on endothelial function; second, to assess the effect of this intervention on markers of immune activation and chronic inflammation, and on plasma HIV-RNA below 50 copies/ml.

• Phase: Phase 4
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: S.F.L. van Lelyveld
• Treatments: Abacavir; Maraviroc

Criteria

Inclusion Criteria:

• Age > 18 years

• HIV-1 infection

• Treatment with antiretroviral regimen containing abacavir for at least the previous 3 months

• Undetectable plasma HIV RNA (50 cp/ml) for at least 6 months (one 'blip' allowed, which is defined as a detectable plasma HIV-RNA level between 50 and 400 copies/ml, preceded and followed by undetectable (<50 copies/ml) plasma HIV-RNA measurements)

• CD4+ cell count > 200 cells/μL

• Signed informed consent

Exclusion Criteria:

• Pregnancy

• Breastfeeding

• Allergy for peanuts or soya

• Hypersensitivity for maraviroc

• Treatment of underlying malignancy

• Acute infection in the preceding 30 days

• Renal insufficiency requiring hemodialysis

• Acute or decompensated chronic hepatitis

• Modification of antiretroviral regimen in the previous 3 months