Please use this identifier to cite or link to this item:
http://cmuir.cmu.ac.th/jspui/handle/6653943832/51004
Title: | Preexposure chemoprophylaxis for HIV prevention in men who have sex with men |
Authors: | Robert M. Grant Javier R. Lama Peter L. Anderson Vanessa McMahan Albert Y. Liu Lorena Vargas Pedro Goicochea Martín Casapía Juan Vicente Guanira-Carranza Maria E. Ramirez-Cardich Orlando Montoya-Herrera Telmo Fernández Valdilea G. Veloso Susan P. Buchbinder Suwat Chariyalertsak Mauro Schechter Chariyalertsak Linda Gail Bekker Kenneth H. Mayer Esper Georges Kallás K. Rivet Amico Kathleen Mulligan Lane R. Bushma Robert J. Hance Carmela Ganoza Patricia Defechereux Brian Postle Furong Wang Jeff McConnell Jia Hua Zheng Jeanny Lee James F. Rooney Howard S. Jaff Ana I. Martinez David N. Burns David V. Glidden |
Authors: | Robert M. Grant Javier R. Lama Peter L. Anderson Vanessa McMahan Albert Y. Liu Lorena Vargas Pedro Goicochea Martín Casapía Juan Vicente Guanira-Carranza Maria E. Ramirez-Cardich Orlando Montoya-Herrera Telmo Fernández Valdilea G. Veloso Susan P. Buchbinder Suwat Chariyalertsak Mauro Schechter Chariyalertsak Linda Gail Bekker Kenneth H. Mayer Esper Georges Kallás K. Rivet Amico Kathleen Mulligan Lane R. Bushma Robert J. Hance Carmela Ganoza Patricia Defechereux Brian Postle Furong Wang Jeff McConnell Jia Hua Zheng Jeanny Lee James F. Rooney Howard S. Jaff Ana I. Martinez David N. Burns David V. Glidden |
Keywords: | Medicine |
Issue Date: | 30-Dec-2010 |
Abstract: | Background Antiretroviral chemoprophylaxis before exposure is a promising approach for the prevention of human immunodeficiency virus (HIV) acquisition. Methods We randomly assigned 2499 HIV-seronegative men or transgender women who have sex with men to receive a combination of two oral antiretroviral drugs, emtricitabine and tenofovir disoproxil fumarate (FTC-TDF), or placebo once daily. All subjects received HIV testing, risk-reduction counseling, condoms, and management of sexually transmitted infections. Results The study subjects were followed for 3324 person-years (median, 1.2 years; maximum, 2.8 years). Of these subjects, 10 were found to have been infected with HIV at enrollment, and 100 became infected during follow-up (36 in the FTC-TDF group and 64 in the placebo group), indicating a 44% reduction in the incidence of HIV (95% confidence interval, 15 to 63; P = 0.005). In the FTC-TDF group, the study drug was detected in 22 of 43 of seronegative subjects (51%) and in 3 of 34 HIV-infected subjects (9%) (P<0.001). Nausea was reported more frequently during the first 4 weeks in the FTC-TDF group than in the placebo group (P<0.001). The two groups had similar rates of serious adverse events (P = 0.57). Conclusions Oral FTC-TDF provided protection against the acquisition of HIV infection among the subjects. Detectable blood levels strongly correlated with the prophylactic effect. (Funded by the National Institutes of Health and the Bill and Melinda Gates Foundation; ClinicalTrials.gov number, NCT00458393.). © 2010 Massachusetts Medical Society. |
URI: | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=78650549662&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/51004 |
ISSN: | 15334406 00284793 |
Appears in Collections: | CMUL: Journal Articles |
Files in This Item:
There are no files associated with this item.
Items in CMUIR are protected by copyright, with all rights reserved, unless otherwise indicated.