drugset / Trial / NCT03282240
Safety and Immunogenicity of High-Dose Quadrivalent Influenza Vaccine in Participants ≥65 Years in the US
RandomizedParallel-groupDouble-blindPrevention
Summary
This randomized, modified double-blind, active-controlled, multi-center trial assessed the safety and immunogenicity of the high-dose quadrivalent influenza vaccine (QIV-HD) compared to either the licensed or investigational high-dose trivalent influenza vaccine (TIV-HD) in adults.
Timeline
- Start
- 2017-09-08
- Primary completion
- 2017-11-02
- Completion
- 2018-04-19
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Investigational TIV-HD2 | Vaccine | 0.5 ml | Intramuscular |
| Comparator | Licensed TIV-HD1 | Vaccine | 0.5 ml | Intramuscular |
| Subject | QIV-HD | Vaccine | 0.7 ml | Intramuscular |