drugset / Trial / NCT00841763

Safety, Tolerability and Immunogenicity of Two Doses of Adjuvanted Monovalent Influenza Vaccine Administered to Healthy Adult and Elderly Subjects

NCT00841763

Phase 3 Completed 3647 enrolled Novartis Novartis Vaccines · collab
RandomizedParallel-groupDouble-blindPrevention

Summary

The present study, phase III, randomized, controlled, observer-blind, multicenter study, will evaluate safety, tolerability and immunogenicity of two doses of an adjuvanted monovalent influenza vaccine compared with an adjuvanted interpandemic trivalent influenza vaccine in a population of healthy adult and elderly subjects.

Timeline

Start
2008-10
Primary completion
2009-04
Completion
2009-11

Drugs

EvaluationDrugModalityDoseRoute
Comparator Adjuvanted trivalent influenza virus vaccine Vaccine 0.5 ml Intramuscular
Subject Agrippal Vaccine 0.5 ml Intramuscular
Subject FLUAD-H5N1 Vaccine 0.5 ml Intramuscular

Indications