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Clinical trialNCT00194519CompletedPhase 3Interventional

Herpes Simplex Virus Type 2 (HSV-2) Suppression to Prevent HIV Transmission

SponsorUniversity of WashingtonEnrollment3,408HIV InfectionHerpes Simplex, GenitalSexually Transmitted Diseases
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The University of Washington has received funding to conduct a proof-of-concept trial to assess the impact of suppression of genital herpes on HIV infectiousness. This study (the Partners in Prevention Study) will enroll HIV discordant heterosexual couples in which the HIV-infected partner is co-infected with herpes simplex virus type 2 (HSV-2) to test the efficacy of twice daily (bid) acyclovir (400 mg) given to the HIV-infected partner to prevent transmission to his/her HIV negative partner(s). This randomized, double-blind, placebo-controlled proof-of-concept trial will provide evidence for the efficacy of HSV-2 suppression with daily acyclovir on HIV transmission among HIV-discordant couples among whom the HIV-positive partner is also HSV-2 seropositive with CD4 \>250. The researchers hypothesis is that, by decreasing the frequency and amount of genital HIV shedding, standard doses of daily acyclovir 400 mg bid will reduce the rate of HIV transmission by 50% in HIV-discordant couples among whom the HIV-infected partner is HSV-2 positive. Under the study protocol version 4.1.1, 3000 HIV-discordant heterosexual couples in which the HIV-positive partner is HSV-2 positive and has a CD4 count \>250 will be recruited; participants will be followed for up to 2 years. A 4% per year HIV incidence in the placebo arm is assumed. The first study site began enrolling participants on 17 November 2005. As of September 2006, 14 sites in Eastern and Southern Africa had participated in recruiting the 2300 HIV-discordant couples enrolled to date.

Investigators

The overall officials registered on this study. Names that resolve to a FindMyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

13 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Botswana
  • Botswana-Harvard Partnership

    Gabarone, Botswana

Kenya
  • Moi University - Indiana University

    Eldoret, Kenya

  • Kemri - Ucsf

    Kisumu, Kenya

  • University of Nairobi

    Nairobi, Kenya

  • Partners Study Thika Site

    Thika, Kenya

Rwanda
  • Projet San Francisco-Emory University

    Kigali, Rwanda

South Africa
  • University of Cape Town

    Cape Town, South Africa

  • Perinatal Hiv Research Unit, University of Witswatersrand

    Johannesburg, South Africa

  • Reproductive Health and Hiv Research Unit

    Johannesburg, South Africa

Tanzania
  • Kilimanjaro Christian Medical College-Harvard University

    Moshi, Tanzania

Uganda
  • Mulago Hospital - Idi

    Kampala, Uganda

Zambia
  • Zambia-Emory Hiv Research Project

    Lusaka, Zambia

  • Zambia-Emory Hiv Research Project

    Ndola/Kitwe, Zambia

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

Generic acyclovirPlacebo
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
30 Nov 2004
Primary completion
30 Nov 2009
Completion
31 Mar 2010
Last update posted
12 Oct 2018
Registered enrollment
3,408
Registry id
NCT00194519

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 4 Nov 2026. Registry facts are shown as registered by the study sponsor; FindMyKOL does not interpret them.