drugset / Trial / NCT00382187
Safety and Immunogenicity of Two Adjuvanted and One Non-adjuvanted H5N1 Influenza Vaccine in Adults
RandomizedParallel-groupSingle-blindPrevention
Summary
The present study aims to evaluate safety and immunogenicity of two doses, administered three weeks apart, and a 6 month booster dose, of two influenza vaccines containing 7.5 micrograms or 15 micrograms of H5N1 influenza antigen, and of a non-adjuvanted influenza vaccine containing 15 micrograms of H5N1 influenza antigen, in adults
Timeline
- Start
- 2006-11
- Primary completion
- 2008-01
- Completion
- 2008-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | MF59 adjuvanted H5N1 influenza vaccine | Vaccine | 7.5 ug | — |
| Subject | MF59 adjuvanted H5N1 influenza vaccine | Vaccine | 15 ug | — |
| Subject | non-adjuvanted influenza vaccine | Vaccine | 15 ug | — |