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HSV-2 Suppression to Reduce Maternal HIV-1 RNA Levels During Pregnancy and Breastfeeding (VIP)

Primary Purpose

HIV Infections, Herpes Simplex

Status
Completed
Phase
Phase 2
Locations
Kenya
Study Type
Interventional
Intervention
valacyclovir
placebo
Sponsored by
University of Washington
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV Infections focused on measuring Disease Transmission, Vertical, valacyclovir, Randomized Controlled Trials, HIV, herpes, Herpesvirus 2, Human, HIV Seronegativity

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • HIV-1 seropositive
  • HSV-2 seropositive
  • Plans to deliver in Nairobi
  • Resides and plans to remain in Nairobi for 12 months postpartum
  • 18 years of age or older
  • CD4 count>250 cells/μl

Exclusion Criteria:

  • indication for highly active antiretroviral therapy (e.g., WHO stage III or IV)
  • hypersensitivity to valacyclovir or acyclovir

Sites / Locations

  • Mathare North City Clinic

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

1

2

Arm Description

500 mg oral valacyclovir twice daily from 34 weeks gestation to 1 year postpartum

oral placebo twice daily from 34 weeks gestation to 1 year postpartum

Outcomes

Primary Outcome Measures

Mean Change in HIV-1 Levels in Plasma Between 34 and 38 Weeks Gestation
Calculated as log10 plasma viral load at 34 weeks gestation - log10 plasma viral load at 38 weeks gestation

Secondary Outcome Measures

Vertical HIV-1 Transmission
Mother-to-child HIV transmission

Full Information

First Posted
September 13, 2007
Last Updated
November 28, 2018
Sponsor
University of Washington
Collaborators
Royalty Research Fund - University of Washington, Puget Sound Partners for Global Health, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
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1. Study Identification

Unique Protocol Identification Number
NCT00530777
Brief Title
HSV-2 Suppression to Reduce Maternal HIV-1 RNA Levels During Pregnancy and Breastfeeding
Acronym
VIP
Official Title
HSV-2 Suppression to Reduce Maternal HIV-1 RNA Levels During Pregnancy and Breastfeeding
Study Type
Interventional

2. Study Status

Record Verification Date
November 2018
Overall Recruitment Status
Completed
Study Start Date
April 2008 (undefined)
Primary Completion Date
August 2010 (Actual)
Study Completion Date
August 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Washington
Collaborators
Royalty Research Fund - University of Washington, Puget Sound Partners for Global Health, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
In this study, we will determine whether treating pregnant and breastfeeding women co-infected with human immunodeficiency virus type 1 (HIV-1) and herpes simplex virus type 2 (HSV-2) with daily valacyclovir will reduce HIV-1 levels in plasma, genital, and breast milk and will decrease the risk of mother-to-child HIV-1 transmission (MTCT).
Detailed Description
Each year over 500,000 children become HIV-1-infected in sub-Saharan Africa after exposure to maternal virus in blood, genital secretions, and breast milk. Identifying feasible, safe, and affordable interventions that prevent mother-to-child transmission remains a priority for HIV-1 prevention research. Interventions to reduce breast milk HIV-1 transmission are lacking and most urgently needed. We propose a randomized clinical trial to determine whether incorporating HSV-2 suppression with valacyclovir into standard prevention of mother-to-child HIV-1 transmission regimens will reduce plasma, cervical, and breast milk HIV-1 RNA levels and risk of transmission among HIV-1-infected and HSV-2-seropositive women. We plan to enroll a total of 148 HIV-1 and HSV-2 co-infected pregnant women with CD4>200 cells/μl who seek antenatal care prior to 32 weeks gestation at a clinic in Nairobi, Kenya. Women will be randomized to receive either valacyclovir suppressive therapy or placebo at 34 weeks gestation and mother-infant pairs will be followed for 12 months postpartum. Follow-up visits will be scheduled at 38 weeks gestation; birth; 2, 6, 10 and 14 weeks; and 6, 9, and 12 months postpartum. Maternal blood, genital, and breast milk specimens obtained at follow-up visits will be used to determine the effect of valacyclovir suppressive therapy on plasma and breast milk HIV-1 RNA levels. Infant filter paper specimens for HIV-1 DNA assays will be collected at birth; 2, 6, 10 and 14 weeks; and 6, 9, and 12 months in order to compare the proportion of infants acquiring HIV-1 by 12 months in the two study arms and determine the timing of HIV-1 infection. In addition, we will monitor maternal and infant renal function in preparation for a larger randomized clinical trial in Africa. The results of this study will help guide the design of a multi-site clinical trial with adequate power to determine the effect of HSV-2 suppression on vertical (MTCT) transmission of HIV-1 infection.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections, Herpes Simplex
Keywords
Disease Transmission, Vertical, valacyclovir, Randomized Controlled Trials, HIV, herpes, Herpesvirus 2, Human, HIV Seronegativity

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
148 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
500 mg oral valacyclovir twice daily from 34 weeks gestation to 1 year postpartum
Arm Title
2
Arm Type
Placebo Comparator
Arm Description
oral placebo twice daily from 34 weeks gestation to 1 year postpartum
Intervention Type
Drug
Intervention Name(s)
valacyclovir
Other Intervention Name(s)
Valtrex
Intervention Description
500 mg oral valacyclovir twice daily from 34 weeks gestation to 1 year postpartum
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
oral placebo twice daily from 34 weeks gestation to 1 year postpartum
Primary Outcome Measure Information:
Title
Mean Change in HIV-1 Levels in Plasma Between 34 and 38 Weeks Gestation
Description
Calculated as log10 plasma viral load at 34 weeks gestation - log10 plasma viral load at 38 weeks gestation
Time Frame
4 weeks
Secondary Outcome Measure Information:
Title
Vertical HIV-1 Transmission
Description
Mother-to-child HIV transmission
Time Frame
1 year postpartum

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: HIV-1 seropositive HSV-2 seropositive Plans to deliver in Nairobi Resides and plans to remain in Nairobi for 12 months postpartum 18 years of age or older CD4 count>250 cells/μl Exclusion Criteria: indication for highly active antiretroviral therapy (e.g., WHO stage III or IV) hypersensitivity to valacyclovir or acyclovir
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Carey Farquhar, MD, MPH
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mathare North City Clinic
City
Nairobi
Country
Kenya

12. IPD Sharing Statement

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HSV-2 Suppression to Reduce Maternal HIV-1 RNA Levels During Pregnancy and Breastfeeding

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