drugset / Trial / NCT03301051

Efficacy, Safety, and Immunogenicity of a Plant-Derived Quadrivalent Virus-Like Particles (VLPs) Influenza Vaccine in Adults

NCT03301051

Phase 3 Completed 10160 enrolled Medicago
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

EvaluationDrugModalityDoseRoute
Subject Quadrivalent VLP Vaccine Vaccine 30 ug Intramuscular
Subject Quadrivalent VLP Vaccine Vaccine 0.5 ml Intramuscular

Indications