drugset / Trial / NCT00309647

Study to Evaluate the Safety and Immunogenicity of Pandemic Monovalent (H5N1) Influenza Vaccines (Whole Virus Formulation) in Adults 18 and 60 Years of Age

NCT00309647 ↗

Phase 1 Completed 400 enrolled GlaxoSmithKline
RandomizedParallel-groupSingle-blindPrevention

Summary

Today, the leading contender for the next pandemic of influenza is H5N1, a strain of avian virus. Prevention and control of a pandemic will depend on the rapid production and worldwide distribution of specific pandemic vaccines. Candidate 'pandemic-like' vaccines must be developed and tested in clinical trials to determine the most optimal formulation and the best vaccination schedule.This study is designed to test in healthy adults aged between 18-60 years the reactogenicity and immunogenicity of one and two administrations of a candidate pandemic H5N1 vaccine formulated from Whole Virus. The vaccines contain different antigen doses. For each dose, adjuvanted vaccine will be compared to the plain vaccine in order to detect the optimal formulation for immunization against the H5N1 influenza strain.

Timeline

Start
2006-03-29
Primary completion
2006-11-01
Completion
2006-11-16

Drugs

EvaluationDrugModalityDoseRoute
Comparator Influenza Monovalent Whole virus (H5N1) Vaccine — Intramuscular
Subject Influenza Monovalent Whole virus (H5N1) adjuvanted vaccine Vaccine — Intramuscular

Indications