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Maraviroc-containing regimens safe, tolerable when taken for HIV prevention

NIH/National Institute of Allergy and Infectious Diseases

24-Feb-2016 - Maraviroc, an oral drug used to treat HIV infection, is safe and well-tolerated when taken daily as pre-exposure prophylaxis (PrEP) to prevent HIV infection by HIV-uninfected men who have sex with men (MSM) at increased risk for acquiring HIV. These findings from the Phase 2 HPTN 069/ACTG 5305 trial were presented today 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.

In the study, 406 MSM in the United States and Puerto Rico were randomly assigned to take either once-daily maraviroc alone, maraviroc plus TDF, maraviroc plus emtricitabine, or TDF and emtricitabine. Investigators found that the maraviroc-containing regimens were as safe and well-tolerated as TDF and emtricitabine. Five participants became infected with HIV during the study. These participants had low, variable or undetectable drug levels, likely indicating they were not consistently using PrEP.

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. More information about the study is available on ClinicalTrials.gov using identifier NCT01505114.

PRESENTATIONS: Roy Gulick et al. HPTN 069/ACTG 5305: Phase II Study of Maraviroc-Based Regimens for HIV PrEP in MSM. Session: Expanding the Toolbox for Prevention

Ian McGowan et al. PrEP Impact on T-cell Activation and Explant Infection: HPTN 069/ACTG 5305 Substudy. Session: Expanding the Toolbox for Prevention

WHO: NIAID Director Anthony S. Fauci, M.D., and Carl Dieffenbach, Ph.D., director of NIAID's Division of AIDS, are available to discuss the findings.

CONTACT: To schedule interviews, please contact Hillary Hoffman, (301) 402-1663, hillary.hoffman@nih.gov .

###

NIAID conducts and supports research--at NIH, throughout the United States, and worldwide--to study the causes of infectious and immune-mediated diseases, and to develop better means of preventing, diagnosing and treating these illnesses. News releases, fact sheets and other NIAID-related materials are available on the NIAID website.

About the National Institutes of Health (NIH): NIH, the nation's medical research agency, includes 27 Institutes and Centers and is a component of the U.S. Department of Health and Human Services. NIH is the primary federal agency conducting and supporting basic, clinical, and translational medical research, and is investigating the causes, treatments, and cures for both common and rare diseases. For more information about NIH and its programs, visit http://www.nih.gov/.


Media Contact

Hillary Hoffman
hillary.hoffman@nih.gov
301-402-1663
 @NIAIDNews
http://www.niaid.nih.gov 

Source: http://www.eurekalert.org/pub_releases/2016-02/nioa-mrs022416.php


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