drugset / Trial / NCT00970177

Immunogenicity, Safety and Tolerability of Two Doses of Adjuvanted and Non-adjuvanted Swine Origin A/H1N1 Monovalent Influenza Vaccine in Healthy Subjects 18 or More Years of Age

NCT00970177 ↗

Phase 3 Completed 812 enrolled Novartis Vaccines
RandomizedParallel-groupSingle-blindPrevention

Summary

This present study, randomized, single-blind, dose-ranging, multicenter study, will evaluate immunogenicity, safety and tolerability of two doses of an adjuvanted and not-adjuvanted new swine-origin influenza A/H1N1 virus monovalent subunit vaccine in healthy adult and elderly subjects. A booster dose will be administered 12 months after the first vaccination.

Timeline

Start
2009-08
Primary completion
2009-10
Completion
2011-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Monovalent A/H1N1 influenza vaccine Vaccine 3.75 ug Intramuscular
Subject Monovalent A/H1N1 influenza vaccine Vaccine 7.5 ug Intramuscular
Subject Monovalent A/H1N1 influenza vaccine Vaccine 15 ug Intramuscular

Indications