drugset / Trial / NCT01107587

Study to Assess the Safety of GSK Biologicals' Liquid Human Rotavirus Vaccine in Healthy Infants

NCT01107587 ↗

Phase 1 Completed 50 enrolled GlaxoSmithKline
RandomizedParallel-groupQuadruple-blindPrevention

Summary

The purpose of this study is to assess the reactogenicity and safety of GSK Biologicals' liquid human rotavirus vaccine in healthy infants aged 6 to 16 weeks at the time of the first dose of vaccination.

Timeline

Start
2010-04-13
Primary completion
2010-06-28
Completion
2010-06-28

Drugs

EvaluationDrugModalityDoseRoute
Subject 444563 Vaccine — Oral

Indications