Safety and Efficacy of a Dapivirine Vaginal Ring for HIV Prevention in Women

Annaléne Nel(International Partnership for Microbicides), Neliëtte van Niekerk(International Partnership for Microbicides), Saidi Kapiga(London School of Hygiene & Tropical Medicine), Linda‐Gail Bekker(Desmond Tutu HIV Foundation), Cynthia Gama(Mwanza Intervention Trials Unit), Katherine Gill(Desmond Tutu HIV Foundation), Anatoli Kamali(Mwanza Intervention Trials Unit), Philip Kotze(Mwanza Intervention Trials Unit), Cheryl Louw(Mwanza Intervention Trials Unit), Zonke Mabude(Mwanza Intervention Trials Unit), Nokuthula Miti(Mwanza Intervention Trials Unit), Sylvia Kusemererwa(Mwanza Intervention Trials Unit), Hugo Tempelman(Mwanza Intervention Trials Unit), Hannelie Carstens(International Partnership for Microbicides), Bríd Devlin(International Partnership for Microbicides), Michelle Isaacs(International Partnership for Microbicides), Mariëtte Malherbe(International Partnership for Microbicides), Winél Mans(International Partnership for Microbicides), Jeremy Nuttall(International Partnership for Microbicides), Marisa Russell(International Partnership for Microbicides), Smangaliso Ntshele(International Partnership for Microbicides), Marlie Smit(International Partnership for Microbicides), Leonard Nichiren Solai(International Partnership for Microbicides), Patrick Spence(International Partnership for Microbicides), John Steytler(International Partnership for Microbicides), Kathleen Marie Windle(International Partnership for Microbicides), Maarten Borremans(Mwanza Intervention Trials Unit), Sophie Resseler(Mwanza Intervention Trials Unit), Jens Van Roey(Janssen (Belgium)), Wim Parys(Janssen (Belgium)), Tony Vangeneugden(Janssen (Belgium)), Ben Van Baelen(Janssen (Belgium)), Zeda Rosenberg(International Partnership for Microbicides)
New England Journal of Medicine
November 30, 2016
Cited by 462Open Access
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Abstract

BACKGROUND: The incidence of human immunodeficiency virus (HIV) infection remains high among women in sub-Saharan Africa. We evaluated the safety and efficacy of extended use of a vaginal ring containing dapivirine for the prevention of HIV infection in 1959 healthy, sexually active women, 18 to 45 years of age, from seven communities in South Africa and Uganda. METHODS: In this randomized, double-blind, placebo-controlled, phase 3 trial, we randomly assigned participants in a 2:1 ratio to receive vaginal rings containing either 25 mg of dapivirine or placebo. Participants inserted the rings themselves every 4 weeks for up to 24 months. The primary efficacy end point was the rate of HIV type 1 (HIV-1) seroconversion. RESULTS: A total of 77 participants in the dapivirine group underwent HIV-1 seroconversion during 1888 person-years of follow-up (4.1 seroconversions per 100 person-years), as compared with 56 in the placebo group who underwent HIV-1 seroconversion during 917 person-years of follow-up (6.1 seroconversions per 100 person-years). The incidence of HIV-1 infection was 31% lower in the dapivirine group than in the placebo group (hazard ratio, 0.69; 95% confidence interval [CI], 0.49 to 0.99; P=0.04). There was no significant difference in efficacy of the dapivirine ring among women older than 21 years of age (hazard ratio for infection, 0.63; 95% CI, 0.41 to 0.97) and those 21 years of age or younger (hazard ratio, 0.85; 95% CI, 0.45 to 1.60; P=0.43 for treatment-by-age interaction). Among participants with HIV-1 infection, nonnucleoside reverse-transcriptase inhibitor resistance mutations were detected in 14 of 77 participants in the dapivirine group (18.2%) and in 9 of 56 (16.1%) in the placebo group. Serious adverse events occurred more often in the dapivirine group (in 38 participants [2.9%]) than in the placebo group (in 6 [0.9%]). However, no clear pattern was identified. CONCLUSIONS: Among women in sub-Saharan Africa, the dapivirine ring was not associated with any safety concerns and was associated with a rate of acquisition of HIV-1 infection that was lower than the rate with placebo. (Funded by the International Partnership for Microbicides; ClinicalTrials.gov number, NCT01539226 .).


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