drugset / Trial / NCT04596696

Evaluate Immunogenicity, Safety, and Reactogenicity of Rotavac in Healthy Infants in Vietnam

NCT04596696

Phase 3 Completed 360 enrolled Bharat Biotech International Limited
NaSingle-groupOpen-labelPrevention

Summary

An open label study to evaluate immunogenicity, safety, and reactogenicity of Rotavac® (live attenuated oral rotavirus vaccine) as a 3-dose series in healthy infants aged between 6 weeks and 8 weeks in Vietnam

Timeline

Start
2017-12-20
Primary completion
2018-12-30
Completion
2019-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject ROTAVAC® Vaccine Oral

Indications