drugset / Trial / NCT02680002
Assess the Safety & Immunogenicity of Stored Inactivated Influenza H5N1 Virus Vaccine Given With & Without Stored MF59 Adjuvant
Phase 2
Completed
422 enrolled
Biomedical Advanced Research and Development Authority
PPD Development, LP · collab
RandomizedParallel-groupTriple-blindPrevention
Summary
The main purpose of this study is to assess the usability of long-term stored H5N1 antigen and adjuvant. The study is designed to assist in stockpile management by assessing the safety, reactogenicity, and immunogenicity long-term stored influenza A/Vietnam/H5N1 vaccine when administered with or without MF59® adjuvant.
Timeline
- Start
- 2016-03
- Primary completion
- 2016-05-13
- Completion
- 2017-03-31
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | A/Vietnam/H5N1 virus vaccine | Vaccine | 7.5 ug | Intramuscular |
| Subject | A/Vietnam/H5N1 virus vaccine | Vaccine | 15 ug | Intramuscular |
| Subject | A/Vietnam/H5N1 virus vaccine | Vaccine | 90 ug | Intramuscular |