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

October 9, 2018 updated by: Connie Celum, University of Washington

Phase III Randomized Placebo-Controlled Trial of HSV-2 Suppression to Prevent HIV Transmission Among HIV-Discordant Couples

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.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Herpes simplex virus type-2 (HSV-2) is the primary cause of genital ulcers and one of the most prevalent sexually transmitted diseases worldwide. Consistently, over 30 studies have found HSV-2 infection to be a risk factor for HIV acquisition with an overall relative risk of 2.1 in the studies that demonstrated HSV-2 preceded HIV infection. A recent study of HIV-discordant couples from Rakai, Uganda, has shown that at all levels of HIV viral load in the HIV-positive partner, HSV-2 infection in the susceptible partner increased the per-contact risk of acquisition of HIV five-fold, and GUD in the HIV-source partner increased the per-contact risk of HIV transmission five-fold. As strong as these epidemiological data are, an intervention trial is required to define the clinical and public health significance of these findings.

This trial will directly answer the extent to which HSV-2 infection increases infectiousness of HIV/HSV-2 co-infected persons and the relative reduction in HIV transmission among HSV-2 seropositive persons treated with daily suppressive antiviral therapy. Acyclovir has an acceptable safety profile for widespread STD treatment and is inexpensive, well-tolerated, and episodic and long-term suppressive therapy has not been associated with increased acyclovir resistance. Given high HSV-2 seroprevalence in HIV-infected persons (70-80%) and high HIV incidence in populations with high prevalence of HSV-2 infection worldwide, this approach could have great public health importance by providing a safe, acceptable, and cost-effective method to reduce HIV transmission among HIV-infected persons who are also HSV-2 seropositive.

Sites that have enrolled couples in this study include: Johannesburg (2 sites) and Cape Town, South Africa; Gaborone, Botswana; Kitwe/Ndola and Lusaka, Zambia; Nairobi, Kisumu, Eldoret and Thika, Kenya; Moshi, Tanzania; Kampala, Uganda; and Kigali, Rwanda.

Study Type

Interventional

Enrollment (Actual)

3408

Phase

  • Phase 3

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Botswana
      • Gabarone, Botswana
        • Botswana-Harvard Partnership
  • Kenya
      • Eldoret, Kenya
        • Moi University - Indiana University
      • Kisumu, Kenya
        • Kemri - Ucsf
      • Nairobi, Kenya
        • University of Nairobi
      • Thika, Kenya
        • Partners Study Thika Site
  • Rwanda
      • Kigali, Rwanda
        • Projet San Francisco-Emory University
  • South Africa
      • Cape Town, South Africa
        • University of Cape Town
      • Johannesburg, South Africa
        • Perinatal HIV Research Unit, University of Witswatersrand
      • Johannesburg, South Africa
        • Reproductive Health and HIV Research Unit
  • Tanzania
      • Moshi, Tanzania
        • Kilimanjaro Christian Medical College-Harvard University
  • Uganda
      • Kampala, Uganda
        • Mulago Hospital - IDI
  • Zambia
      • Lusaka, Zambia
        • Zambia-Emory HIV Research Project
      • Ndola/Kitwe, Zambia
        • Zambia-Emory HIV Research Project

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

Potential index (HIV-infected) participants must meet the following criteria (by self-report, unless otherwise indicated) in order to be eligible for inclusion in the study:

  • Of legal age to provide independent informed consent for research per local regulations and guidelines.
  • Able and willing to provide written informed consent to be screened for and to take part in the study. (Note: Index participants who are not willing to provide genital tract specimens for HIV viral load quantitation, but are willing to undergo all other study procedures, will be considered eligible for inclusion in the study.)
  • Part of a heterosexual couple in which one partner meets the study eligibility criteria for index participants and the other partner meets the study eligibility criteria for partner participants. Couples are defined as partners who are sexually active and plan to remain in the relationship for at least one year. Each site will develop appropriate criteria for determining whether a couple is likely to remain in the relationship (i.e., married, duration of partnership, cohabitation, have children).
  • Has had vaginal intercourse with the partner participant at least three times in the last three months.
  • Plans to maintain his/her relationship with the partner participant for the next 24 months.
  • HIV-infected based on positive EIA.
  • HSV-2-seropositive based on the Focus HSV-2 EIA (performed by study staff) with an index ratio of at least 3.5 or if Focus EIA IN 1.1-3.4, confirmed by HSV-2 WB dot-blot performed at the UW.
  • CD4 cell count (performed by study staff) of at least 250 cells/mm3.
  • No history of any clinical AIDS-defining diagnoses.
  • Able and willing to provide adequate locator information for study retention purposes, as defined by local standard operating procedures.

Potential partner (HIV-uninfected at enrollment) participants must meet the following criteria (by self-report, unless otherwise indicated) in order to be eligible for inclusion in the study:

  • Of legal age to provide independent informed consent for research per local regulations and guidelines.
  • Able and willing to provide written informed consent to be screened for and to take part in the study.
  • Part of a heterosexual couple in which one partner meets the study eligibility criteria for index participants and the other partner meets the study eligibility criteria for partner participants.
  • Has had vaginal intercourse with the study partner at least three times in the last three months.
  • Plans to maintain his/her relationship with the index participant for the next 24 months.
  • HIV-uninfected based on negative HIV EIA tests.
  • Able and willing to provide adequate locator information for study retention purposes, as defined by local standard operating procedures.

Exclusion Criteria:

Potential index (HIV-infected) participants who meet any of the following criteria (by self-report, unless otherwise indicated) will be excluded from the study:

  • Current use of combination antiretroviral therapy
  • Known history of adverse reaction to acyclovir.
  • Known history of persistent genital ulcers unresponsive to episodic acyclovir therapy.
  • Known plans to re-locate or travel away from the study site for more than two consecutive months during the next 24 months.
  • Pregnant, based on participant self-report or urine testing performed by study staff. (Note: Self-reported pregnancy is adequate for exclusion from the study. A documented negative test performed by study staff is required for inclusion.)

Potential partner participants who meet any of the following criteria (by self-report, unless otherwise indicated) will be excluded from the study:

  • Has had sexual intercourse with a partner other than the index participant in the last two months.
  • Known plans to re-locate or travel away from the study site for more than two consecutive months during the next 24 months.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: PREVENTION
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: QUADRUPLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
PLACEBO_COMPARATOR: Placebo
Drug: Placebo
twice-daily oral
ACTIVE_COMPARATOR: Acyclovir
Drug: Generic acyclovir
400 mg twice-daily oral

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Sequence-verified HIV-transmission from index to partner participant
Time Frame: March 2009
March 2009

Secondary Outcome Measures

Outcome Measure
Time Frame
Measure effect of viral load, gender and other factors on HIV transmission
Time Frame: March 2009
March 2009
Assess adherence to acyclovir suppressive therapy
Time Frame: March 2009
March 2009
Assess effect of twice daily acyclovir on the frequency of genital ulcers
Time Frame: March 2009
March 2009
Assess effect of twice daily acyclovir on plasma HIV viral load
Time Frame: March 2009
March 2009
Assess effects of twice daily acyclovir on the sexual behaviors
Time Frame: March 2009
March 2009
Assess host immunologic and virologic determinants of HIV transmission
Time Frame: March 2009
March 2009

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

University of Washington

Collaborators

Bill and Melinda Gates Foundation

Investigators

  • Study Director: Jairam Lingappa, MD, PhD,, University of Washington

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

November 1, 2004

Primary Completion (ACTUAL)

November 1, 2009

Study Completion (ACTUAL)

March 1, 2010

Study Registration Dates

First Submitted

September 13, 2005

First Submitted That Met QC Criteria

September 13, 2005

First Posted (ESTIMATE)

September 19, 2005

Study Record Updates

Last Update Posted (ACTUAL)

October 12, 2018

Last Update Submitted That Met QC Criteria

October 9, 2018

Last Verified

October 1, 2018

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • STUDY00000867
  • Gates Foundation Grant #26469

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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