drugset / Trial / NCT00197249

Comparative Study in Healthy Adults Aged 18-50 Yrs Administered With Hepatyrix or Havrix+Typherix or Tiphim Vi, to Compare Reactogenicity & Immunogenicity

NCT00197249 ↗

Phase 3 Completed 1034 enrolled GlaxoSmithKline
RandomizedParallel-groupOpen-labelPrevention

Summary

To evaluate the immunogenicity, reactogenicity and safety of Hepatyrix when compared to the concomitant administration of Typherix and Havrix, and when compared to the administration of monovalent vaccines, Havrix or Typhim Vi. Furthermore, the study will evaluate the persistence of anti-Vi and anti-HAV antibodies up to 36 months after administration of the first dose of the study vaccine.

Timeline

Start
2002-05
Primary completion
2003-06
Completion
2005-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Hepatyrix Vaccine — Intramuscular