Title
Brief Report: Routine Use of Oral PrEP in a Phase 2 Rectal Microbicide Study of Tenofovir Reduced-Glycerin 1% Gel (MTN-017)
Date Issued
15 August 2019
Access level
open access
Resource Type
journal article
Author(s)
Liu A.Y.
Norwood A.
Gundacker H.
Carballo-Diéguez A.
Johnson S.
Patterson K.
Bekker L.G.
Chariyalertsak S.
Chitwarakorn A.
Holtz T.H.
Mayer K.H.
Zorrilla C.
Buchbinder S.
Piper J.M.
Cranston R.D.
Publisher(s)
Wolters Kluwer Health
Abstract
Background: As daily oral preexposure prophylaxis (PrEP) becomes standard for HIV prevention, routine use of PrEP is likely to increase within clinical trials of novel preventive agents. We describe the prevalence and characteristics of participants reporting nonstudy oral PrEP use within Microbicide Trials Network-017 (MTN-017), a phase 2 trial of a rectal microbicide. Setting and Methods: One hundred ninety-five HIV-uninfected men who have sex with men and transgender women were enrolled and followed in MTN-017 across 8 sites in the United States, Thailand, South Africa, and Peru from 2013 to 2015. Nonstudy oral PrEP use was recorded on case report forms and progress notes. Characteristics of PrEP users and non-PrEP users were compared using tests of statistical significance. Results: Overall, 11% of participants reported nonstudy oral PrEP use, all from the San Francisco (SF) site, accounting for 58% (22/38) of participants enrolled in SF. There was a higher median number of sex partners reported in the past 8 weeks before enrollment among oral PrEP users vs. nonusers (7 vs. 2, P = 0.02). Most PrEP users (18/22, 82%) began PrEP treatment during screening/after enrollment, and most (19/22, 86%) decided to continue oral PrEP after study completion. Conclusion: Nonstudy oral PrEP use in the first phase 2 study of tenofovir reduced-glycerin 1% gel was high at a single site in SF where community PrEP availability and use was expanding. Investigators should consider the evolving context of nonstudy oral PrEP use across trial sites when designing and interpreting trials of novel biomedical prevention modalities.
Start page
516
End page
520
Volume
81
Issue
5
Language
English
OCDE Knowledge area
Farmacología, Farmacia
Dermatología, Enfermedades venéreas
Subjects
Scopus EID
2-s2.0-85069819169
PubMed ID
Source
Journal of Acquired Immune Deficiency Syndromes
ISSN of the container
15254135
Sponsor(s)
A.Y.L. and S.B. have received study drug from Gilead Sciences for studies in which they are investigators. K.H.M. has unrestricted research grants from Gilead and Viiv and has been on Scientific Advisory Boards for Gilead and Merck. R.D.C. has received royalties from Uptodate and institutional research funding from ABIVAX pharmaceuticals. The remaining authors have no conflicts of interest to disclose.
Supported by National Institute of Allergy and Infectious Diseases (UM1AI068633, UM1AI068615, UM1AI106707), with co-funding from the Eunice Kennedy Shriver National Institute of Child Health and Human Development and the National Institute of Mental Health, all components of the U.S. National Institutes of Health. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health or the other institutions represented. Gilead Sciences provided FTC/TDF and CONRAD provided RG-TFV.
Sources of information:
Directorio de Producción Científica
Scopus