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Assessment of Community Transmission of Sabin Type 2 Virus in Bangladesh

Primary Purpose

Vaccine Virus Shedding

Status
Unknown status
Phase
Phase 3
Locations
Bangladesh
Study Type
Interventional
Intervention
tOPV
bOPV
IPV
Sponsored by
University of Virginia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Vaccine Virus Shedding

Eligibility Criteria

42 Days - 48 Days (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • A male or female infant at least 6 weeks of age (42-48 days) at the time of enrollment
  • For the Special Immunization Activity (SIA) only, being age 5 years or younger at the time of the SIA
  • An infant whose parent or guardian's primary residence, at the time of first Expanded Program on Immunization (EPI) vaccinations, is a village selected to receive polio vaccine.
  • Written informed consent obtained from the parent or guardian of the participant, prior to the participants's first study vaccination

Exclusion Criteria:

  • History of prior polio vaccination (in the 810 infants enrolled at 6 weeks of age only)
  • Hypersensitivity to the active substance or any component in the vaccine
  • Subjects with uncorrected congenital malformation
  • Infants with known or suspected immunodeficiency

Sites / Locations

  • International Centre for Diarrhoeal Disease Research, Bangladesh

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

tOPV + IPV

bOPV + IPV

bOPV + 2 IPV

Arm Description

tOPV (6, 10, and 14 weeks) + IPV (14 weeks) Randomized to receive tOPV plus IPV boost

bOPV (6, 10, and 14 weeks) + IPV (14 weeks) Randomized to receive bOPV plus 1 IPV boost

bOPV (6, 10, and 14 weeks) + IPV (14 and 18 weeks) Randomized to receive bOPV plus 2 IPV boost

Outcomes

Primary Outcome Measures

fecal shedding of type 2 Sabin virus by quantitative reverse transcription polymerase chain reaction (RT-qPCR) in 60% of infants that did not receive the mOPV2 challenge
The transmission rate of type 2 Sabin virus in the 60% of the enrolled infants that did not receive the mOPV2 challenge between Arm A vs Arm B, Arm A vs Arm C, and Arm B and Arm C.

Secondary Outcome Measures

fecal shedding of type 2 Sabin virus by RT-qPCR in 40% of infants that received the mOPV2 challenge
Individual protection to type 2 poliovirus from different vaccination schedules

Full Information

First Posted
June 18, 2015
Last Updated
October 24, 2016
Sponsor
University of Virginia
Collaborators
International Centre for Diarrhoeal Disease Research, Bangladesh, Bill and Melinda Gates Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT02477046
Brief Title
Assessment of Community Transmission of Sabin Type 2 Virus in Bangladesh
Official Title
Assessment of Community Transmission of Sabin Type 2 Virus in Bangladesh
Study Type
Interventional

2. Study Status

Record Verification Date
October 2016
Overall Recruitment Status
Unknown status
Study Start Date
April 2015 (undefined)
Primary Completion Date
July 2016 (Actual)
Study Completion Date
June 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Virginia
Collaborators
International Centre for Diarrhoeal Disease Research, Bangladesh, Bill and Melinda Gates Foundation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The Strategic Advisory Group of Experts on Immunization (SAGE) has set a plan to replace trivalent oral polio vaccine (tOPV) with bivalent OPV (bOPV) plus inactivated polio vaccine (IPV) in routine immunization globally, to be instituted in 2015-2016. At the community level, the impact of the change from tOPV + IPV to bOPV + IPV on Sabin virus fecal-oral transmission (duration of circulation, degree of genetic reversion) and the persistence of environmental contamination are unknown. Also unknown is the impact of the change from tOPV to bOPV on community circulation of Sabin 2 after a special immunization (SI) activity with monovalent oral poliovirus type 2 (mOPV2). Finally it is unknown at the level of an individual child if type 2 fecal shedding will be limited by cross-protection from oral vaccination with Sabin type 1 and 3. The investigators propose to measure at a community level transmission of Sabin 2 virus in Bangladesh, a low income country, where fecal-oral transmission and environmental exposures are high, comparing transmission in the setting of vaccination with tOPV+IPV vs. bOPV+IPV. The study will be conducted in 67 villages in Matlab, Bangladesh, using a cluster-randomized study design. Villages in Matlab will be randomly assigned to receive as part of routine immunization (RI) activities: (1) tOPV (6,10,14 weeks) plus IPV at 14 weeks; (2) bOPV (6,10, 14 weeks) plus IPV at 14 weeks; or (3) bOPV (6,10, 14 weeks) plus IPV at 14 and 18 weeks. Community and environmental surveillance for Sabin 2 virus will be conducted in each village over the 9 month period of these RI activities. In addition, a SI activity with mOPV2 will occur 9 months into the study to model an outbreak response. For the 6 months following the mOPV2 challenge, the impact of the different vaccination regimens on Sabin 2 transmission in the community will be determined, as well as individual level protection (as measured by fecal shedding from days 7-70 after mOPV2 challenge).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vaccine Virus Shedding

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
810 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
tOPV + IPV
Arm Type
Experimental
Arm Description
tOPV (6, 10, and 14 weeks) + IPV (14 weeks) Randomized to receive tOPV plus IPV boost
Arm Title
bOPV + IPV
Arm Type
Experimental
Arm Description
bOPV (6, 10, and 14 weeks) + IPV (14 weeks) Randomized to receive bOPV plus 1 IPV boost
Arm Title
bOPV + 2 IPV
Arm Type
Experimental
Arm Description
bOPV (6, 10, and 14 weeks) + IPV (14 and 18 weeks) Randomized to receive bOPV plus 2 IPV boost
Intervention Type
Biological
Intervention Name(s)
tOPV
Intervention Description
administered per protocol
Intervention Type
Biological
Intervention Name(s)
bOPV
Intervention Description
administered per protocol
Intervention Type
Biological
Intervention Name(s)
IPV
Intervention Description
administered per protocol
Primary Outcome Measure Information:
Title
fecal shedding of type 2 Sabin virus by quantitative reverse transcription polymerase chain reaction (RT-qPCR) in 60% of infants that did not receive the mOPV2 challenge
Description
The transmission rate of type 2 Sabin virus in the 60% of the enrolled infants that did not receive the mOPV2 challenge between Arm A vs Arm B, Arm A vs Arm C, and Arm B and Arm C.
Time Frame
10 weeks following mOPV2 challenge at month 9 of the study
Secondary Outcome Measure Information:
Title
fecal shedding of type 2 Sabin virus by RT-qPCR in 40% of infants that received the mOPV2 challenge
Description
Individual protection to type 2 poliovirus from different vaccination schedules
Time Frame
10 weeks following mOPV2 challenge at month 9 of the study

10. Eligibility

Sex
All
Minimum Age & Unit of Time
42 Days
Maximum Age & Unit of Time
48 Days
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: A male or female infant at least 6 weeks of age (42-48 days) at the time of enrollment For the Special Immunization Activity (SIA) only, being age 5 years or younger at the time of the SIA An infant whose parent or guardian's primary residence, at the time of first Expanded Program on Immunization (EPI) vaccinations, is a village selected to receive polio vaccine. Written informed consent obtained from the parent or guardian of the participant, prior to the participants's first study vaccination Exclusion Criteria: History of prior polio vaccination (in the 810 infants enrolled at 6 weeks of age only) Hypersensitivity to the active substance or any component in the vaccine Subjects with uncorrected congenital malformation Infants with known or suspected immunodeficiency
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
William A Petri, Jr., MD, PhD
Organizational Affiliation
University of Virginia
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mami Taniuchi, PhD
Organizational Affiliation
University of Virginia
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
K Zaman, MBBS, PhD
Organizational Affiliation
International Centre for Diarrhoeal Disease Research, Bangladesh
Official's Role
Principal Investigator
Facility Information:
Facility Name
International Centre for Diarrhoeal Disease Research, Bangladesh
City
Matlab
Country
Bangladesh

12. IPD Sharing Statement

Citations:
PubMed Identifier
25378579
Citation
Taniuchi M, Begum S, Uddin MJ, Platts-Mills JA, Liu J, Kirkpatrick BD, Chowdhury AH, Jamil KM, Haque R, Petri WA Jr, Houpt ER. Kinetics of poliovirus shedding following oral vaccination as measured by quantitative reverse transcription-PCR versus culture. J Clin Microbiol. 2015 Jan;53(1):206-11. doi: 10.1128/JCM.02406-14. Epub 2014 Nov 5.
Results Reference
background
PubMed Identifier
34932560
Citation
Famulare M, Wong W, Haque R, Platts-Mills JA, Saha P, Aziz AB, Ahmed T, Islam MO, Uddin MJ, Bandyopadhyay AS, Yunus M, Zaman K, Taniuchi M. Multiscale model for forecasting Sabin 2 vaccine virus household and community transmission. PLoS Comput Biol. 2021 Dec 21;17(12):e1009690. doi: 10.1371/journal.pcbi.1009690. eCollection 2021 Dec.
Results Reference
derived
PubMed Identifier
28693854
Citation
Taniuchi M, Famulare M, Zaman K, Uddin MJ, Upfill-Brown AM, Ahmed T, Saha P, Haque R, Bandyopadhyay AS, Modlin JF, Platts-Mills JA, Houpt ER, Yunus M, Petri WA Jr. Community transmission of type 2 poliovirus after cessation of trivalent oral polio vaccine in Bangladesh: an open-label cluster-randomised trial and modelling study. Lancet Infect Dis. 2017 Oct;17(10):1069-1079. doi: 10.1016/S1473-3099(17)30358-4. Epub 2017 Jul 7.
Results Reference
derived
Available IPD and Supporting Information:
Available IPD/Information Type
Statistical Analysis Plan
Available IPD/Information URL
https://idmod.sharepoint.com/projects/_layouts/15/guestaccess.aspx?guestaccesstoken=3%2bxJO%2bcBwXx6PfMuzCQmu8ESB0X7mhLPtowTTLaYTmY%3d&docid=02ab39752ccb14c10bdfd61c0a731e6ff&rev=1

Learn more about this trial

Assessment of Community Transmission of Sabin Type 2 Virus in Bangladesh

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