mOPV1: Monovalent Oral Poliovirus Vaccine Type 1 Intestinal and Humoral Immunity Study

Sponsor

Centers for Disease Control and Prevention (U.S. Fed)

Overall Status

Completed

CT.gov ID

NCT03722004

Collaborator

International Centre for Diarrhoeal Disease Research, Bangladesh (Other)

1,256

Enrollment

Location

Arms

Actual Duration (Months)

104.5

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This is an open-label phase IV randomized clinical trial that will assess intestinal and humoral immunity among infants who receive a combination of monovalent oral poliovirus vaccine type 1 and fractional dose of inactivated poliovirus vaccine, monovalent oral poliovirus vaccine type 1 only, and bivalent oral poliovirus vaccine only.

Condition or Disease	Intervention/Treatment	Phase
Poliomyelitis	Biological: mOPV1 Biological: bOPV Biological: fIPV	Phase 4

Detailed Description

The risk for circulating vaccine-derived poliovirus (cVDPV) will increase in the years immediately after the cessation of oral poliovirus vaccine (OPV) use in routine immunization programs. Judicious use of type-specific monovalent OPV (mOPV) will be necessary for outbreak response to prevent further paralytic infections and transmission; however, data on the intestinal and humoral immunity induced by mOPV1 are very limited. Furthermore, the additional benefit of fractional dose inactivated poliovirus vaccine (fIPV) on type 1 immunity when given with mOPV1 is unclear. Data on intestinal and humoral immunity of mOPV type 1 (mOPV1) and combination use of mOPV1 and fractional dose of IPV (fIPV) are urgently needed and would be used to inform guidelines for type 1 outbreak response in a post-OPV world. In the immediate future, a strategy of shifting from bivalent OPV (bOPV) to mOPV1 as part of supplemental immunization activities in endemic countries is under consideration but data on intestinal and humoral immunity to support this change does not exist. This trial is designed to address both areas in which data are lacking.

Healthy infants 5 weeks of age will be enrolled at two study clinics in Dhaka, Bangladesh, and randomized to one of four study arms: mOPV1 + fIPV at 6 weeks, mOPV1 + fIPV at 14 weeks, mOPV1 only, and bOPV only. Infants will be followed-up until 18 weeks of age by clinic and household visits. Blood and stool specimens will be collected to test for vaccine response (humoral immunity) and vaccine virus shedding (intestinal immunity).

Study Design

Study Type:

Interventional

Actual Enrollment :

1256 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

None (Open Label)

Primary Purpose:

Other

Official Title:

Intestinal and Humoral Immunity of Monovalent Oral Poliovirus Vaccine Type 1 When Administered With and Without Fractional Inactivated Poliovirus Vaccine

Actual Study Start Date :

Dec 18, 2018

Actual Primary Completion Date :

Dec 19, 2019

Actual Study Completion Date :

Dec 19, 2019

Arms and Interventions

Arm	Intervention/Treatment
Active Comparator: mOPV1 + fIPV 6 weeks mOPV1 administered at 6, 10, and 14 weeks and fIPV at 6 weeks.	Biological: mOPV1 Monovalent oral poliovirus vaccine type 1 is a type-specific, live, attenuated oral poliovirus vaccine that protects against poliovirus type 1. Biological: fIPV Fractional dose of inactivated poliovirus vaccine that protects against types 1, 2, and 3 (all polio serotypes). Given as a 0.1 milliliter (mL) dose (fractional) by intradermal injection in lieu of the full 0.5mL dose that is given intramuscularly.
Active Comparator: mOPV1 + fIPV 10 weeks mOPV1 administered at 6, 10, and 14 weeks and fIPV at10 weeks.	Biological: mOPV1 Monovalent oral poliovirus vaccine type 1 is a type-specific, live, attenuated oral poliovirus vaccine that protects against poliovirus type 1. Biological: fIPV Fractional dose of inactivated poliovirus vaccine that protects against types 1, 2, and 3 (all polio serotypes). Given as a 0.1 milliliter (mL) dose (fractional) by intradermal injection in lieu of the full 0.5mL dose that is given intramuscularly.
Active Comparator: mOPV1 only mOPV1 administered at 6, 10, and 14 weeks.	Biological: mOPV1 Monovalent oral poliovirus vaccine type 1 is a type-specific, live, attenuated oral poliovirus vaccine that protects against poliovirus type 1.
Active Comparator: bOPV only bOPV administered at 6, 10, and 14 weeks.	Biological: bOPV Bivalent oral poliovirus vaccine is a live, attenuated oral poliovirus vaccine that protects against poliovirus types 1 and 3.

Outcome Measures

Primary Outcome Measures

Vaccine response [Measured four weeks after administration of study vaccine(s). Vaccine response will be measured at 10 weeks, 14 weeks, and 18 weeks of age after 1, 2, and 3 doses of OPV, respectively.]
Dichotomous (yes/no) variable defined as participants who are either seronegative (<1:8 titers) at baseline who become seropositive (≥1:8) after vaccination (seroconversion) or participants who demonstrate a four-fold rise in titers after vaccination between two specimens, e.g. a change from 1:8 to 1:32, after adjusting for expected decay in maternal antibodies. Antibody titers at 6 weeks of age will be the starting point for the expected decline in maternal antibodies, assuming at half-life of 28 days.
Vaccine virus particles [Measured 7 and 14 days after administration of the study vaccine. For Arms B, C, and D, this will be after administration of the first mOPV1 or bOPV dose. For Arms A, B, and C, this will be after the mOPV1 challenge dose at 14 weeks of age.]
Presence or absence of vaccine virus particles in stool specimens.

Secondary Outcome Measures

Reciprocal antibody titers [Measured four weeks after administration of study vaccine(s). Vaccine response will be measured at 10 weeks, 14 weeks, and 18 weeks of age after 1, 2, and 3 doses of OPV, respectively.]
Variable of the observed reciprocal antibody titer results.

Eligibility Criteria

Criteria

Ages Eligible for Study:

35 Days to 41 Days

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Yes

Inclusion Criteria:

Healthy infants 5 weeks of age (range: 35-41 days).
Parents that consent for participation in the full length of the study.
Parents that are able to understand and comply with planned study procedures.

Exclusion Criteria:

Parents and infants who are unable to participate in the full length of the study.
A diagnosis or suspicion of immunodeficiency disorder either in the infant or in an immediate family member.
A diagnosis or suspicion of bleeding disorder that would contraindicate parenteral administration of fIPV or collection of blood by venipuncture.
Evidence of a chronic medical condition identified by a study medical officer during physical exam.
Infection or illness at the enrolment visit (i.e., 5 weeks of age) that a study medical officer judges would prevent the start of study activities at 6 weeks of age (i.e., blood collection and vaccination).
Receipt of any polio vaccine (OPV or IPV/fIPV) before enrolment based upon documentation or parental recall.
Known allergy/sensitivity or reaction to polio vaccine, or its contents.
Infants from multiple births. Infants from multiple births will be excluded because the infant(s) who is/are not enrolled would likely receive OPV through routine immunization and transmit vaccine poliovirus to the enrolled infant.
Infants from premature births (<37 weeks of gestation).