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
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |