drugset / Trial / NCT02214225
A Study to Evaluate the Immunogenicity and Safety of bioCSL Quadrivalent Influenza Vaccine (QIV) in Adults Aged 18 Years and Above.
RandomizedParallel-groupQuadruple-blindPrevention
Summary
This is a study to assess the immune (antibody) response and safety of a bioCSL split virion, inactivated quadrivalent influenza vaccine, in comparison with a US licensed 2014/2015 trivalent influenza vaccine (bioCSL TIV-1), and a trivalent influenza vaccine containing the alternate B strain (bioCSL TIV-2), in healthy adult volunteers aged 18 years and above.
Timeline
- Start
- 2014-08
- Primary completion
- 2014-11
- Completion
- 2015-04
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Influvactetra | Vaccine | 0.5 ml | Intramuscular |
| Comparator | Trivalent Influenza Vaccine (TIV-1) | Vaccine | 0.5 ml | Intramuscular |
| Comparator | Trivalent Influenza Vaccine (TIV-2) | Vaccine | 0.5 ml | Intramuscular |