drugset / Trial / NCT03602053

Summary

The study is being conducted to evaluate and compare the immunogenicity of ROTAVAC® and ROTAVAC 5D 28 days after the last dose of the vaccine, when administered to infants in a three-dose schedule at 6, 10 and 14 weeks of age. The study will also assess the reactogenicity of the vaccine 7 days after each vaccination and safety from first vaccination up to 4 weeks after the last vaccination with ROTAVAC® and ROTAVAC 5D, and of Rotarix® when administered to infants in a two-dose schedule at 6 and 10 weeks of age.

Timeline

Start
2019-01-22
Primary completion
2019-10-04
Completion
2019-10-04

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject ROTAVAC 5D Vaccine 0.5 ml Oral
Subject ROTAVAC® Vaccine 0.5 ml Oral
Comparator Rotarix Vaccine 1.5 ml Oral