drugset / Trial / NCT01612000
Safety and Immunogenicity of PanBlok Influenza Vaccine in Healthy Adults
RandomizedParallel-groupQuadruple-blindPrevention
Summary
The purpose of this study is to investigate the safety and immunogenicity of a recombinant hemagglutinin (rHA) influenza vaccine derived from A/Indonesia/05/2005 (H5N1) administered at 3 dose levels in adjuvanted (SE) rHA formulations and 1 dose levels in an un-adjuvanted rHA formulation.
Timeline
- Start
- 2012-05
- Primary completion
- 2013-08
- Completion
- 2013-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | PanBlok | Vaccine | 3.8 ug | Intramuscular |
| Subject | PanBlok | Vaccine | 7.5 ug | Intramuscular |
| Subject | PanBlok | Vaccine | 15 ug | Intramuscular |
| Subject | rHA adjuvant | Unknown | 2 % | Intramuscular |