To prevent HIV infection by HIV-uninfected men who have sex with men (MSM) at increased risk for acquiring HIV, taking maraviroc, an oral drug used to treat HIV infection, is safe and well-tolerated when taken daily as pre-exposure prophylaxis (PrEP).
These findings from the Phase 2 HPTN 069/ACTG 5305 trial were presented at the Conference on Retroviruses and Opportunistic Infections in Boston. The trial was sponsored by the National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health, and conducted by the NIH-funded HIV Prevention Trials Network, in collaboration with the AIDS Clinical Trials Group.
A daily pill called Truvada containing the antiretroviral drugs tenofovir disoproxil fumarate (TDF) and emtricitabine currently is the only PrEP regimen approved by the Food and Drug Administration. TDF and emtricitabine interfere with viral replication after HIV has entered cells. Maraviroc blocks HIV from entering cells and concentrates in the rectum and genital tract.
The researchers also reported results from a substudy evaluating the impact of these PrEP regimens on colorectal tissue samples from 55 participants. Previous work in HIV-infected people had suggested that maraviroc may increase immune T-cell activation in rectal tissue, which potentially could increase susceptibility to HIV infection. However, the researchers did not observe increased T-cell activation in the samples.
Viral suppression experiments with tissue samples taken from study volunteers provided a preliminary indication that maraviroc alone may be less effective at preventing HIV infection than combination PrEP regimens. The HPTN 069/ACTG 5305 investigators also are assessing the safety and tolerability of maraviroc-containing regimens in women at risk of sexually acquiring HIV.