drugset / Trial / NCT01162590

Study to Evaluate the Reactogenicity and Safety of Rotarix™ in Chinese Adults

NCT01162590

Phase 1 Completed 52 enrolled GlaxoSmithKline
RandomizedParallel-groupTriple-blindPrevention

Summary

The purpose of this study is to assess the safety of Rotarix ™ when administered in healthy adults aged 18 to 45 years in China.

Timeline

Start
2010-03-01
Primary completion
2010-03-31
Completion
2010-03-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Rotarix Vaccine Oral

Indications