HIV Prevention Among Men Who Have Sex With Men: Tenofovir Alafenamide Combination Preexposure Prophylaxis Versus Placebo

Author:

Zivich Paul N12ORCID,Cole Stephen R1,Edwards Jessie K1ORCID,Glidden David V3ORCID,Das Moupali4,Shook-Sa Bonnie E5ORCID,Shao Yongwu4,Mehrotra Megha L34,Adimora Adaora A16ORCID,Eron Joseph J16ORCID

Affiliation:

1. Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill , Chapel Hill, North Carolina , USA

2. Institute of Global Health and Infectious Diseases, School of Medicine, University of North Carolina at Chapel Hill , Chapel Hill, North Carolina , USA

3. Department of Epidemiology and Biostatistics, University of California , San Francisco, California, USA

4. Gilead Sciences , Foster City, California , USA

5. Department of Biostatistics, Gillings School of Global Public Health, University of North Carolina at Chapel Hill , Chapel Hill, North Carolina , USA

6. Division of Infectious Diseases, School of Medicine, University of North Carolina at Chapel Hill , Chapel Hill, North Carolina , USA

Abstract

Abstract Background While noninferiority of tenofovir alafenamide and emtricitabine (TAF/FTC) as preexposure prophylaxis (PrEP) for the prevention of human immunodeficiency virus (HIV) has been shown, interest remains in its efficacy relative to placebo. We estimate the efficacy of TAF/FTC PrEP versus placebo for the prevention of HIV infection. Methods We used data from the DISCOVER and iPrEx trials to compare TAF/FTC to placebo. DISCOVER was a noninferiority trial conducted from 2016 to 2017. iPrEx was a placebo-controlled trial conducted from 2007 to 2009. Inverse probability weights were used to standardize the iPrEx participants to the distribution of demographics and risk factors in the DISCOVER trial. To check the comparison, we evaluated whether risk of HIV infection in the shared tenofovir disoproxil fumarate and emtricitabine (TDF/FTC) arms was similar. Results Notable differences in demographics and risk factors occurred between trials. After standardization, the difference in risk of HIV infection between the TDF/FTC arms was near zero. The risk of HIV with TAF/FTC was 5.8 percentage points lower (95% confidence interval [CI], −2.0% to −9.6%) or 12.5-fold lower (95% CI, .02 to .31) than placebo standardized to the DISCOVER population. Conclusions There was a reduction in HIV infection with TAF/FTC versus placebo across 96 weeks of follow-up. Clinical Trials Registration NCT02842086 and NCT00458393.

Funder

National Institute of Allergy and Infectious Diseases

Division

of Acquired Immunodeficiency Syndrome

NIH

Bill and Melinda Gates Foundation

Gilead Sciences

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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