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
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
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
NCT ID
NCT00530777
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)
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
Citations:
PubMed Identifier
10459959
Citation
Dabis F, Msellati P, Meda N, Welffens-Ekra C, You B, Manigart O, Leroy V, Simonon A, Cartoux M, Combe P, Ouangre A, Ramon R, Ky-Zerbo O, Montcho C, Salamon R, Rouzioux C, Van de Perre P, Mandelbrot L. 6-month efficacy, tolerance, and acceptability of a short regimen of oral zidovudine to reduce vertical transmission of HIV in breastfed children in Cote d'Ivoire and Burkina Faso: a double-blind placebo-controlled multicentre trial. DITRAME Study Group. DIminution de la Transmission Mere-Enfant. Lancet. 1999 Mar 6;353(9155):786-92. doi: 10.1016/s0140-6736(98)11046-2.
Results Reference
background
PubMed Identifier
15821396
Citation
Iliff PJ, Piwoz EG, Tavengwa NV, Zunguza CD, Marinda ET, Nathoo KJ, Moulton LH, Ward BJ, Humphrey JH; ZVITAMBO study group. Early exclusive breastfeeding reduces the risk of postnatal HIV-1 transmission and increases HIV-free survival. AIDS. 2005 Apr 29;19(7):699-708. doi: 10.1097/01.aids.0000166093.16446.c9.
Results Reference
background
PubMed Identifier
17267842
Citation
Drake AL, John-Stewart GC, Wald A, Mbori-Ngacha DA, Bosire R, Wamalwa DC, Lohman-Payne BL, Ashley-Morrow R, Corey L, Farquhar C. Herpes simplex virus type 2 and risk of intrapartum human immunodeficiency virus transmission. Obstet Gynecol. 2007 Feb;109(2 Pt 1):403-9. doi: 10.1097/01.AOG.0000251511.27725.5c. Erratum In: Obstet Gynecol. 2007 Apr;109(4):1002-3.
Results Reference
background
PubMed Identifier
16319261
Citation
Chen KT, Segu M, Lumey LH, Kuhn L, Carter RJ, Bulterys M, Abrams EJ; New York City Perinatal AIDS Collaborative Transmission Study (PACTS) Group. Genital herpes simplex virus infection and perinatal transmission of human immunodeficiency virus. Obstet Gynecol. 2005 Dec;106(6):1341-8. doi: 10.1097/01.AOG.0000185917.90004.7c.
Results Reference
background
Citation
Whitehead S, Bollen L, Leelawiwat W, et al. Maternal HSV-2 Cervicovaginal Shedding Increases the Risk of Intra-partum HIV-1 Transmission. 14th Conference on Retroviruses and Opportunistic Infections. Los Angeles, 2007.
Results Reference
background
PubMed Identifier
16303067
Citation
Duffus WA, Mermin J, Bunnell R, Byers RH, Odongo G, Ekwaru P, Downing R. Chronic herpes simplex virus type-2 infection and HIV viral load. Int J STD AIDS. 2005 Nov;16(11):733-5. doi: 10.1258/095646205774763298.
Results Reference
background
PubMed Identifier
9291329
Citation
Mole L, Ripich S, Margolis D, Holodniy M. The impact of active herpes simplex virus infection on human immunodeficiency virus load. J Infect Dis. 1997 Sep;176(3):766-70. doi: 10.1086/517297.
Results Reference
background
PubMed Identifier
10432323
Citation
Mofenson LM, Lambert JS, Stiehm ER, Bethel J, Meyer WA 3rd, Whitehouse J, Moye J Jr, Reichelderfer P, Harris DR, Fowler MG, Mathieson BJ, Nemo GJ. Risk factors for perinatal transmission of human immunodeficiency virus type 1 in women treated with zidovudine. Pediatric AIDS Clinical Trials Group Study 185 Team. N Engl J Med. 1999 Aug 5;341(6):385-93. doi: 10.1056/NEJM199908053410601.
Results Reference
background
PubMed Identifier
10432324
Citation
Garcia PM, Kalish LA, Pitt J, Minkoff H, Quinn TC, Burchett SK, Kornegay J, Jackson B, Moye J, Hanson C, Zorrilla C, Lew JF. Maternal levels of plasma human immunodeficiency virus type 1 RNA and the risk of perinatal transmission. Women and Infants Transmission Study Group. N Engl J Med. 1999 Aug 5;341(6):394-402. doi: 10.1056/NEJM199908053410602.
Results Reference
background
PubMed Identifier
9952365
Citation
Shaffer N, Roongpisuthipong A, Siriwasin W, Chotpitayasunondh T, Chearskul S, Young NL, Parekh B, Mock PA, Bhadrakom C, Chinayon P, Kalish ML, Phillips SK, Granade TC, Subbarao S, Weniger BG, Mastro TD. Maternal virus load and perinatal human immunodeficiency virus type 1 subtype E transmission, Thailand. Bangkok Collaborative Perinatal HIV Transmission Study Group. J Infect Dis. 1999 Mar;179(3):590-9. doi: 10.1086/314641.
Results Reference
background
PubMed Identifier
10608756
Citation
Chuachoowong R, Shaffer N, Siriwasin W, Chaisilwattana P, Young NL, Mock PA, Chearskul S, Waranawat N, Chaowanachan T, Karon J, Simonds RJ, Mastro TD. Short-course antenatal zidovudine reduces both cervicovaginal human immunodeficiency virus type 1 RNA levels and risk of perinatal transmission. Bangkok Collaborative Perinatal HIV Transmission Study Group. J Infect Dis. 2000 Jan;181(1):99-106. doi: 10.1086/315179.
Results Reference
background
PubMed Identifier
9631135
Citation
Newell ML. Mechanisms and timing of mother-to-child transmission of HIV-1. AIDS. 1998 May 28;12(8):831-7. doi: 10.1097/00002030-199808000-00004. No abstract available.
Results Reference
background
PubMed Identifier
17314338
Citation
Nagot N, Ouedraogo A, Foulongne V, Konate I, Weiss HA, Vergne L, Defer MC, Djagbare D, Sanon A, Andonaba JB, Becquart P, Segondy M, Vallo R, Sawadogo A, Van de Perre P, Mayaud P; ANRS 1285 Study Group. Reduction of HIV-1 RNA levels with therapy to suppress herpes simplex virus. N Engl J Med. 2007 Feb 22;356(8):790-9. doi: 10.1056/NEJMoa062607.
Results Reference
background
PubMed Identifier
16464276
Citation
Ozouaki F, Ndjoyi-Mbiguino A, Legoff J, Onas IN, Kendjo E, Si-Mohamed A, Mbopi-Keou FX, Malkin JE, Belec L. Genital shedding of herpes simplex virus type 2 in childbearing-aged and pregnant women living in Gabon. Int J STD AIDS. 2006 Feb;17(2):124-7. doi: 10.1258/095646206775455711.
Results Reference
background
PubMed Identifier
11802924
Citation
Conant MA, Schacker TW, Murphy RL, Gold J, Crutchfield LT, Crooks RJ; International Valaciclovir HSV Study Group. Valaciclovir versus aciclovir for herpes simplex virus infection in HIV-infected individuals: two randomized trials. Int J STD AIDS. 2002 Jan;13(1):12-21. doi: 10.1258/0956462021924550.
Results Reference
background
PubMed Identifier
17342670
Citation
Workowski KA, Berman SM. Centers for Disease Control and Prevention sexually transmitted diseases treatment guidelines. Clin Infect Dis. 2007 Apr 1;44 Suppl 3:S73-6. doi: 10.1086/511430. No abstract available.
Results Reference
background
PubMed Identifier
16816068
Citation
Sheffield JS, Hill JB, Hollier LM, Laibl VR, Roberts SW, Sanchez PJ, Wendel GD Jr. Valacyclovir prophylaxis to prevent recurrent herpes at delivery: a randomized clinical trial. Obstet Gynecol. 2006 Jul;108(1):141-7. doi: 10.1097/01.AOG.0000219749.96274.15. Erratum In: Obstet Gynecol. 2006 Sep;108(3 Pt 1):695.
Results Reference
background
PubMed Identifier
16522412
Citation
Andrews WW, Kimberlin DF, Whitley R, Cliver S, Ramsey PS, Deeter R. Valacyclovir therapy to reduce recurrent genital herpes in pregnant women. Am J Obstet Gynecol. 2006 Mar;194(3):774-81. doi: 10.1016/j.ajog.2005.11.051.
Results Reference
background
PubMed Identifier
9790357
Citation
Kimberlin DF, Weller S, Whitley RJ, Andrews WW, Hauth JC, Lakeman F, Miller G. Pharmacokinetics of oral valacyclovir and acyclovir in late pregnancy. Am J Obstet Gynecol. 1998 Oct;179(4):846-51. doi: 10.1016/s0002-9378(98)70176-0.
Results Reference
background
PubMed Identifier
2835389
Citation
Ashley RL, Militoni J, Lee F, Nahmias A, Corey L. Comparison of Western blot (immunoblot) and glycoprotein G-specific immunodot enzyme assay for detecting antibodies to herpes simplex virus types 1 and 2 in human sera. J Clin Microbiol. 1988 Apr;26(4):662-7. doi: 10.1128/jcm.26.4.662-667.1988.
Results Reference
background
PubMed Identifier
9889216
Citation
Panteleeff DD, John G, Nduati R, Mbori-Ngacha D, Richardson B, Kreiss J, Overbaugh J. Rapid method for screening dried blood samples on filter paper for human immunodeficiency virus type 1 DNA. J Clin Microbiol. 1999 Feb;37(2):350-3. doi: 10.1128/JCM.37.2.350-353.1999.
Results Reference
background
PubMed Identifier
24504006
Citation
Roxby AC, Atkinson C, Asbjornsdottir K, Farquhar C, Kiarie JN, Drake AL, Wald A, Boeckh M, Richardson B, Emery V, John-Stewart G, Slyker JA. Maternal valacyclovir and infant cytomegalovirus acquisition: a randomized controlled trial among HIV-infected women. PLoS One. 2014 Feb 4;9(2):e87855. doi: 10.1371/journal.pone.0087855. eCollection 2014.
Results Reference
derived
PubMed Identifier
22852760
Citation
Roxby AC, Liu AY, Drake AL, Kiarie JN, Richardson B, Lohman-Payne BL, John-Stewart GC, Wald A, De Rosa S, Farquhar C. Short communication: T cell activation in HIV-1/herpes simplex virus-2-coinfected Kenyan women receiving valacyclovir. AIDS Res Hum Retroviruses. 2013 Jan;29(1):94-8. doi: 10.1089/AID.2012.0071. Epub 2012 Sep 4.
Results Reference
derived
PubMed Identifier
22509337
Citation
Drake AL, Roxby AC, Kiarie J, Richardson BA, Wald A, John-Stewart G, Farquhar C. Infant safety during and after maternal valacyclovir therapy in conjunction with antiretroviral HIV-1 prophylaxis in a randomized clinical trial. PLoS One. 2012;7(4):e34635. doi: 10.1371/journal.pone.0034635. Epub 2012 Apr 11.
Results Reference
derived
PubMed Identifier
22147786
Citation
Drake AL, Roxby AC, Ongecha-Owuor F, Kiarie J, John-Stewart G, Wald A, Richardson BA, Hitti J, Overbaugh J, Emery S, Farquhar C. Valacyclovir suppressive therapy reduces plasma and breast milk HIV-1 RNA levels during pregnancy and postpartum: a randomized trial. J Infect Dis. 2012 Feb 1;205(3):366-75. doi: 10.1093/infdis/jir766. Epub 2011 Dec 6.
Results Reference
derived
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HSV-2 Suppression to Reduce Maternal HIV-1 RNA Levels During Pregnancy and Breastfeeding
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