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

Drugs

EvaluationDrugModalityDoseRoute
Subject Bivalent Oral Polio Vaccine (bOPV) Vaccine
Subject Imovax Vaccine 0.5 ml
Subject Poliorix™ Vaccine 0.5 ml
Subject Serum Institute of India IPV Vaccine 0.5 ml
Subject Trivalent Oral Polio Vaccine Vaccine Oral
Background Monovalent Oral Polio Vaccine Type 2 (mOPV2) Vaccine Oral

Indications