drugset / Trial / NCT01198769

Immunogenicity and Safety Study of Rotarix TM in Taiwanese Infants Who Received Hepatitis B Immunoglobulin After Birth.

NCT01198769

Phase 4 Completed 15 enrolled GlaxoSmithKline
NaSingle-groupOpen-labelPrevention

Summary

The purpose of this study is to assess immunogenicity and safety of Rotarix TM when administered in healthy Taiwanese infants (aged 6 to 12 weeks at the time of first vaccination) who received Hepatitis B immunoglobulin after birth.

Timeline

Start
2010-11-11
Primary completion
2011-04-18
Completion
2011-04-18

Drugs

EvaluationDrugModalityDoseRoute
Subject Rotarix Vaccine Oral

Indications