drugset / Trial / NCT00510874

Study to Evaluate the Safety and Immune Response of Two-Doses of Candidate Influenza Vaccine GSK 1557484A in Adults

NCT00510874

Phase 1 Completed 780 enrolled GlaxoSmithKline
RandomizedParallel-groupDouble-blindPrevention

Summary

The purpose of this study is to evaluate the safety and immune response of two-doses of GSK Biologicals' candidate influenza vaccine GSK 1557484A with or without adjuvant in adults. The Protocol Posting has been updated in order to comply with the FDA Amendment Act, Sep 2007.

Timeline

Start
2007-07-28
Primary completion
2008-06-17
Completion
2008-10-24

Drugs

EvaluationDrugModalityDoseRoute
Subject Pandemrix Vaccine 3.75 ug Intramuscular
Subject Pumarix Vaccine 3.75 ug Intramuscular

Indications