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NCT Number: NCT03546634

Sero-conversion Study for a Two-dose Schedule of Sabin IPV in China

This study aims to obtain the direct domestic IPV vaccine monitoring data for the CNBG products, and provide scientific evidence for the National Immunization Program and long-term polio vaccine immunization policy.

The overall objective of this research is to determine the seroconversion rates of two reduced Sabin IPV schedules in Chinese children - a 2-dose schedule and a 3-dose schedule.

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Key information

Age range

2 month–18 month

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Shandong Center for Disease Control and Prevention

Jinan, China

About this study

In April 2017, WHO/SAGE recommended that a two-dose, IPV-only schedule can be used after polio eradication, with a schedule seroconversion target of at least 90%. The recommendation was based in part on a study conducted in Cuba using Salk-IPV at 4 months and 8 months of age. However, for domestic Sabin IPVs, there are no such data to support a 2-dose schedule among Chinese infants.Two Sabin IPV products that are available to China's National Immunization Program - produced by Kunming Bio institute and China National Biotec Group (CNBG).The monitoring study on sIPV produced by Kunming Bio institute has already applied for approval.This study aims to obtain the direct domestic IPV vaccine monitoring data for the CNBG products, and provide scientific evidence for the National Immunization Program and long-term polio vaccine immunization policy.

The overall objective of this research is to determine the seroconversion rates of two reduced Sabin IPV schedules in Chinese children - a 2-dose schedule and a 3-dose schedule.

The specific objectives of the study are to:

  • Determine whether the seroconversion rate is above 90% with a 2-dose Sabin IPV schedule, with the first dose given at 4 months and the second dose given ≥4 months after the first dose.
  • Measure neutralizing antibody titers against poliovirus type I, II and III among two-dose Sabin IPV alone schedule, compared with three-dose Sabin IPV alone schedule.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Parent or legal guardian agree to participate in our study.
  • The family is living locally with legal residency status.

Exclusion criteria

  • Parent or legal guardian does not agree to participate in our study.
  • The potential subject has received IPV or OPV before 4 months of age in the two-dose schedule group.
  • The potential subject has one or more contraindications to IPV (although we will note the contraindications).

Treatment and study plan

Sabin IPV

Biological

We select one Sabin IPV product, produced by China National Biotec Group, which is available for China's National Immunization Program in the selected study sites.

Other names: Sabin strain Inactivated Poliovirus Vaccine

Primary outcomes

  1. Seroconversion rate

    Time frame: 10 months

    Determine whether the seroconversion rate is above 90% using a two-dose Sabin IPV alone schedule with the first dose Sabin IPV given at 4 months and the second dose Sabin IPV given ≥4 months after the first dose.

Secondary outcomes

  1. Neutralizing antibody titers

    Time frame: 10 months

    Measure neutralizing antibody titers against poliovirus type I, II and III among two-dose Sabin IPV-only schedules compared with three-dose Sabin IPV alone schedule.

Sponsors and collaborators

Lead sponsor

Centers for Disease Control and Prevention, China

Other Gov

Collaborators

  • Shandong Province Centers for Disease Control and Prevention

Registry information

Official study title

Sero-conversion Study for a Two-dose Schedule of Sabin Strain Inactivated Poliovirus Vaccine in China

Important dates

Study start
2018
Primary completion
2019
Study completion
2020
First posted
Jun 6, 2018
Registry last updated
Jun 24, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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