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Polio End-game Strategies - Poliovirus Type 2 Challenge Study

Primary Purpose

Poliomyelitis

Status
Completed
Phase
Phase 4
Locations
Pakistan
Study Type
Interventional
Intervention
IPV
bOPV
bOPV and IPV
bOPV and IPV and IPV2
tOPV
Sponsored by
Aga Khan University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Poliomyelitis focused on measuring IPV, OPV, tOPV, bOPV, Polio, Endgame, Pakistan

Eligibility Criteria

undefined - 1 Day (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Newborn of either gender born healthy with birth weight 2.0 kg or more, with immediate cry, at the study sites (home or health facility births)
  • Not planning to travel away during entire the study period (birth-154 days; birth 22 weeks).
  • Parents resident of the study area for last 3 month at the time of enrolment
  • Parent/guardian provides informed consent

Exclusion Criteria:

  • Newborns found acutely ill at the time of enrolment and requiring emergent medical care/hospitalization, birth weight below 2.0 kg, cry >2 minutes after birth, or family is planning to be absent during the birth - 154 days study period
  • Refusal of blood testing and cord blood testing
  • Receipt of OPV after birth before eligibility screen
  • Newborns with certain medical conditions i.e., syndromic infants, neonate with petechial or purpura (contraindication of intramuscular injections)
  • A diagnosis or suspicion of immunodeficiency disorder (either in the participant or in a member of the immediate family - e.g. several early infant deaths, household member on chemotherapy) will render the newborn ineligible for the study.

Sites / Locations

  • Rehri goth, Ibrahim Hyderi, Ali Akbar Shah, and Bhens Colony

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm Type

Experimental

Experimental

Experimental

Experimental

Active Comparator

Arm Label

IPV

bOPV

bOPV and IPV

bOPV and IPV and IPV2

tOPV

Arm Description

IPV at birth, 6 weeks, 10 weeks, 14 weeks, followed by tOPV at 18 and 22 weeks

bOPV at birth, 6, 10, and 14 weeks. followed by tOPV at 18 and 22 weeks of age

bOPV at birth, 6, 10 weeks, and IPV+bOPV at 14 weeks, and tOPV at 18 and 22 weeks of age

bOPV at birth, 6, 10 weeks and bOPV+IPV at 14 weeks and tOPV+IPV2 at 18 weeks and tOPV alone at 22 weeks of age

tOPV at birth, 6, 10, 14, 18 and 22 weeks of age

Outcomes

Primary Outcome Measures

Difference in seroprevalence of neutralizing antibodies for type 2 in 19 weeks of age between arms

Secondary Outcome Measures

Seroprevalence of neutralizing antibodies at 18 weeks of age

Full Information

First Posted
July 9, 2014
Last Updated
May 2, 2016
Sponsor
Aga Khan University
Collaborators
World Health Organization, Centers for Disease Control and Prevention, National Institutes of Health (NIH)
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1. Study Identification

Unique Protocol Identification Number
NCT02189811
Brief Title
Polio End-game Strategies - Poliovirus Type 2 Challenge Study
Official Title
Polio End-game Strategies - Poliovirus Type 2 Challenge Study
Study Type
Interventional

2. Study Status

Record Verification Date
May 2016
Overall Recruitment Status
Completed
Study Start Date
September 2014 (undefined)
Primary Completion Date
April 2016 (Actual)
Study Completion Date
May 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Aga Khan University
Collaborators
World Health Organization, Centers for Disease Control and Prevention, National Institutes of Health (NIH)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Poliomyelitis eradication has entered its last phase with only three remaining endemic countries, of which Pakistan is one. There hasn't been a case of wild type poliovirus 2 since 1999, and no case of wild type poliovirus 3 since November 2012. However, paralytic polio resulting from circulating strains of Sabin poliovirus type 2 have become a challenge, and reported from several areas with low population immunity to polio, including in Pakistan. This study will provide data to National Immunization Authorities in order to make strategic decisions about their polio vaccination schedules in anticipation of the global tOPV to bOPV switch and will provide data on the proposed responses to type 2 poliovirus outbreaks.
Detailed Description
The "Polio Endgame Strategy" consists of set of tasks and activities that will be implemented in the next five years. It includes gradual withdrawal of the widely used oral poliomyelitis vaccine (OPV) containing live poliovirus, and will eventually lead to complete eradication and containment of all wild, vaccine-related (VDPV) and Sabin polioviruses. The withdrawal of the type 2 components of trivalent OPV (tOPV) is the key component in the elimination of cVDPVs. This entails strengthening of the immunization system by introducing at least one dose of affordable IPV into the routine immunization schedule globally and then replacing the trivalent OPV with bivalent OPV in all OPV-using countries - setting the stage for eventually ending bOPV use in 2019-2020. Most of the developing countries have an OPV schedule however many developed and European countries follow the IPV only schedule. The current recommendations for polio eradication and endgame is IPV vaccine to be administered together with third OPV dose, which in most countries occurs at 14 weeks of age. This study will assess the protection to type 2 poliovirus achieved after completion of the recommended schedule with bOPV and IPV; it will compare immunogenicity of bOPV + IPV schedule with tOPV only schedule; and will quantify the cross-reactivity of bOPV on inducing type 2 immunological reaction. In addition, it will also provide first data on the proposed outbreak response to type 2 (either with mOPV 2 or with a combination of mOPV 2 and IPV 2). This study will provide data to National Immunization Authorities in order to make strategic decisions about their polio vaccination schedules in anticipation of the global tOPV to bOPV switch and will provide data on the proposed responses to type 2 poliovirus outbreaks.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Poliomyelitis
Keywords
IPV, OPV, tOPV, bOPV, Polio, Endgame, Pakistan

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
900 (Actual)

8. Arms, Groups, and Interventions

Arm Title
IPV
Arm Type
Experimental
Arm Description
IPV at birth, 6 weeks, 10 weeks, 14 weeks, followed by tOPV at 18 and 22 weeks
Arm Title
bOPV
Arm Type
Experimental
Arm Description
bOPV at birth, 6, 10, and 14 weeks. followed by tOPV at 18 and 22 weeks of age
Arm Title
bOPV and IPV
Arm Type
Experimental
Arm Description
bOPV at birth, 6, 10 weeks, and IPV+bOPV at 14 weeks, and tOPV at 18 and 22 weeks of age
Arm Title
bOPV and IPV and IPV2
Arm Type
Experimental
Arm Description
bOPV at birth, 6, 10 weeks and bOPV+IPV at 14 weeks and tOPV+IPV2 at 18 weeks and tOPV alone at 22 weeks of age
Arm Title
tOPV
Arm Type
Active Comparator
Arm Description
tOPV at birth, 6, 10, 14, 18 and 22 weeks of age
Intervention Type
Biological
Intervention Name(s)
IPV
Intervention Description
IPV at birth, 6, 10, 14 weeks of age and tOPV at 18 and 22 weeks of age
Intervention Type
Biological
Intervention Name(s)
bOPV
Intervention Description
bOPV at birth, 6, 10, 14 weeks and tOPV at 18 and 22 weeks of age
Intervention Type
Biological
Intervention Name(s)
bOPV and IPV
Intervention Description
bOPV till week 10, bOPV+IPV at 14 and tOPV at 18 and 22 weeks of age
Intervention Type
Biological
Intervention Name(s)
bOPV and IPV and IPV2
Intervention Description
bOPV till week 10, bOPV+IPV at 14, tOPV+IPV2 at 18 and tOPV at 22 weeks of age
Intervention Type
Biological
Intervention Name(s)
tOPV
Intervention Description
tOPV till 22 weeks of age
Primary Outcome Measure Information:
Title
Difference in seroprevalence of neutralizing antibodies for type 2 in 19 weeks of age between arms
Time Frame
19 weeks of age
Secondary Outcome Measure Information:
Title
Seroprevalence of neutralizing antibodies at 18 weeks of age
Time Frame
18 weeks of age
Other Pre-specified Outcome Measures:
Title
Difference in shedding of poliovirus type 2 in stool in 19 weeks of age between arms
Time Frame
19 weeks of age
Title
Difference in seroprevalence of neutralizing antibodies at 22 weeks of age between arms
Time Frame
22 weeks of age

10. Eligibility

Sex
All
Maximum Age & Unit of Time
1 Day
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Newborn of either gender born healthy with birth weight 2.0 kg or more, with immediate cry, at the study sites (home or health facility births) Not planning to travel away during entire the study period (birth-154 days; birth 22 weeks). Parents resident of the study area for last 3 month at the time of enrolment Parent/guardian provides informed consent Exclusion Criteria: Newborns found acutely ill at the time of enrolment and requiring emergent medical care/hospitalization, birth weight below 2.0 kg, cry >2 minutes after birth, or family is planning to be absent during the birth - 154 days study period Refusal of blood testing and cord blood testing Receipt of OPV after birth before eligibility screen Newborns with certain medical conditions i.e., syndromic infants, neonate with petechial or purpura (contraindication of intramuscular injections) A diagnosis or suspicion of immunodeficiency disorder (either in the participant or in a member of the immediate family - e.g. several early infant deaths, household member on chemotherapy) will render the newborn ineligible for the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ali F Saleem, MBBS,FCPS,MSc
Organizational Affiliation
Aga Khan University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rehri goth, Ibrahim Hyderi, Ali Akbar Shah, and Bhens Colony
City
Karachi
State/Province
Sindh
Country
Pakistan

12. IPD Sharing Statement

Citations:
PubMed Identifier
29477307
Citation
Saleem AF, Yousafzai MT, Mach O, Khan A, Quadri F, Weldon WC, Oberste MS, Zaidi SS, Alam MM, Sutter RW, Zaidi AKM. Evaluation of vaccine derived poliovirus type 2 outbreak response options: A randomized controlled trial, Karachi, Pakistan. Vaccine. 2018 Mar 20;36(13):1766-1771. doi: 10.1016/j.vaccine.2018.02.051. Epub 2018 Feb 21.
Results Reference
derived

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Polio End-game Strategies - Poliovirus Type 2 Challenge Study

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