drugset / Trial / NCT00420316

Long-term Efficacy and Safety of Subjects Approximately 3 Years After Priming With 2 Doses of GSK Bio's HRV Vaccine.

NCT00420316

Phase 3 Completed 1613 enrolled GlaxoSmithKline
RandomizedParallel-groupOpen-labelPrevention

Summary

To assess the long-term efficacy and safety of the subjects during the third year after priming with 2 doses of GSK Biologicals' oral live attenuated HRV vaccine (Rotarix) in the primary vaccination study (102247). The Rotarix vaccine was administered in the primary vaccination study. There was no vaccine/intervention in this long-term efficacy study.

Timeline

Start
2007-02-12
Primary completion
2007-08-08
Completion
2007-08-08

Drugs

EvaluationDrugModalityDoseRoute
Background Rotarix Vaccine Oral

Indications