Safety and efficacy of a dapivirine vaginal ring for HIV prevention in women

dc.contributor.authorNel, A.
dc.contributor.authorVan Niekerk, N.
dc.contributor.authorKapiga, S.
dc.contributor.authorBekker, S.-G.
dc.contributor.authorGama, C.
dc.contributor.authorKamali, A.
dc.contributor.authorKotze, P.
dc.contributor.authorLouw, Cheryl
dc.contributor.authorMAbude, Z.
dc.contributor.authorMiti, N.
dc.contributor.authorKusemererwa, S.
dc.contributor.authorTempelman, H.
dc.contributor.authorCarstens, H.
dc.contributor.authorDevlin, B.
dc.contributor.authorIsaacs, M.
dc.contributor.authorMalherbe, M.
dc.contributor.authorMans, W.
dc.contributor.authorNuttall, J.
dc.contributor.authorRussell, M.
dc.contributor.authorNtshele, S.
dc.contributor.authorSmit, M.
dc.contributor.authorSolai, L.
dc.contributor.authorSpence, P.
dc.contributor.authorSteyler, J.
dc.contributor.authorWindle, K.
dc.contributor.authorBorremans, M.
dc.contributor.authorResseler, S.
dc.contributor.authorVan Roey, J.
dc.contributor.authorParys, W.
dc.contributor.authorVangeneugden, T.
dc.contributor.authorVan Baelen, B.
dc.contributor.authorRosenberg, Z.
dc.date.accessioned2017-01-23T08:39:13Z
dc.date.issued2016-12-01
dc.description.abstractBACKGROUND 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.en_ZA
dc.description.departmentFamily Medicineen_ZA
dc.description.embargo2017-06-01
dc.description.librarianam2017en_ZA
dc.description.sponsorshipSupported by the International Partnership for Microbicides (a not-for-profit product-development partnership), which receives support from the Bill and Melinda Gates Foundation, Irish Aid, the Ministry of Foreign Affairs of Denmark, the Ministry of Foreign Affairs of the Netherlands, the Norwegian Agency for Development Cooperation, the U.K. Department for International Development, the American people through the U.S. Agency for International Development, and the President’s Emergency Plan for AIDS Relief.en_ZA
dc.description.urihttp://www.nejm.orgen_ZA
dc.identifier.citationNel, A, Van Niekerk, S, Kapiga, S, Bekker, L-G, Gama, C, Gill, K, Kamali, A, Kotze, P, Louw, C, Mabude, Z, Miti, N, Kusemererwa, S, Tempelman, H, Carstens, H, Devlin, B, Isaacs, M, Malherbe, M, Mans, W, Nuttall, J, Russell, M, Ntshele, S, Smit, M, Solai, L, Spence, P. Steytler, J, Windle, K, Borremans, M, Resseler, S. Van Roey, J. Parys, W. Vangeneugden, T, Van Baelen, B & Rosenberg, Z 2016, ‘Safety and efficacy of a dapivirine vaginal ring for HIV prevention in women', New England Journal of Medicine, vol. 375, no. 22, pp. 2133-2143.en_ZA
dc.identifier.issn0028-4793 (print)
dc.identifier.issn1533-4406 (online)
dc.identifier.other10.1056/NEJMoa1602046 untranslated
dc.identifier.urihttp://hdl.handle.net/2263/58598
dc.language.isoenen_ZA
dc.publisherMassachusetts Medical Societyen_ZA
dc.rights© 2016 Massachusetts Medical Societyen_ZA
dc.subjectWomenen_ZA
dc.subjectDapivirine ringen_ZA
dc.subjectTreatmenten_ZA
dc.subjectHIV-1 infectionen_ZA
dc.subjectHuman immunodeficiency virus (HIV)en_ZA
dc.subjectVaginal ringen_ZA
dc.subject.otherHealth sciences articles SDG-03
dc.subject.otherSDG-03: Good health and well-being
dc.titleSafety and efficacy of a dapivirine vaginal ring for HIV prevention in womenen_ZA
dc.typeArticleen_ZA

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