drugset / Trial / NCT01560793
Safety and Immunogenicity of a Novel H5N1 Influenza Vaccine in Healthy Adults Age 18-49 Years
NaSingle-groupTriple-blindPrevention
Summary
This study will evaluate the safety and immunogenicity of VAX161B \[STF2.HA5 H5N1\], a recombinant, inactivated, subunit influenza vaccine given as a two dose regimen at a range of doses.
Timeline
- Start
- 2012-06
- Primary completion
- 2013-06
- Completion
- 2013-11
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | VAX161 | Unknown | 1 ug | Intramuscular |
| Subject | VAX161 | Unknown | 2.5 ug | Intramuscular |
| Subject | VAX161 | Unknown | 4 ug | Intramuscular |
| Subject | VAX161 | Unknown | 6 ug | Intramuscular |
| Subject | VAX161 | Unknown | 8 ug | Intramuscular |
| Subject | VAX161 | Unknown | 12 ug | Intramuscular |