drugset / Trial / NCT01831050

Safety and Immunogenicity of 1 or 2 Doses of IPV in Latin American Infants Primed With Bivalent OPV Vaccine

NCT01831050 ↗

RandomizedFactorialSingle-blindPrevention

Summary

This study is a Phase IV, open, randomized, multi-center, controlled vaccine trial conducted in healthy Latin American infants, utilizing one or two supplemental doses of IPV in children previously vaccinated with 3 doses of bOPV. We will examine the impact of supplemental IPV on stool shedding and humoral immunity, as well as intra-IPV manufacturer comparability, and safety.

Timeline

Start
2013-05
Primary completion
2014-04
Completion
2014-12

Outcome

Met primary endpoint

paper Type 2 seroconversion occurred in 19 of 198 infants (9·6%, 95% CI 6·2-14·5) in the bOPV-only groups, 86 of 88 (97·7%, 92·1-99·4) in the tOPV-only group (p<0·0001 vs bOPV-only) PMID 27212429 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Bivalent Oral Polio Vaccine (bOPV) Vaccine — —
Subject Glaxo SmithKline IPV Vaccine 0.5 ml —
Subject Sanofi-Pasteur IPV Vaccine 0.5 ml —
Subject Serum Institute of India IPV Vaccine 0.5 ml —
Subject Trivalent Oral Polio Vaccine (tOPV) Vaccine — Oral
Background Monovalent Oral Polio Vaccine Type 2 (mOPV2) Vaccine — Oral

Indications