drugset / Trial / NCT03301051
Efficacy, Safety, and Immunogenicity of a Plant-Derived Quadrivalent Virus-Like Particles (VLPs) Influenza Vaccine in Adults
RandomizedParallel-groupQuadruple-blindPrevention
Summary
This Phase 3 study is intended to assess the efficacy of the Quadrivalent VLP Influenza Vaccine during the 2017-2018 influenza season in healthy adults 18 to 64 years of age. One dose of Quadrivalent VLP Influenza Vaccine (30 μg/strain) or of placebo will be administered to approximately 10,000 participants
Timeline
- Start
- 2017-08-31
- Primary completion
- 2018-05-02
- Completion
- 2018-05-09
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Quadrivalent VLP Vaccine | Vaccine | 30 ug | Intramuscular |
| Subject | Quadrivalent VLP Vaccine | Vaccine | 0.5 ml | Intramuscular |