drugset / Trial / NCT03789539

Reactogenicity, Safety and Immunogenicity of an Universal Influenza Vaccine Uniflu

NCT03789539 ↗

Phase 1 Unknown 54 enrolled VA Pharma Limited Liability Company
RandomizedParallel-groupQuadruple-blindPrevention

Summary

This is a single-site, randomized, double-blind, placebo-controlled study of Uniflu in fifty four (54) volunteers 18-60 years of age with a dose escalation. All subjects will receive an intramuscular (IM) injection twice,with a 21 days interval between treatments.

Timeline

Start
2018-06-02
Primary completion
2018-12-02
Completion
2018-12-31

Drugs

EvaluationDrugModalityDoseRoute
Comparator Uniflu Vaccine 20 ug Intramuscular
Comparator Uniflu Vaccine 40 ug Intramuscular

Indications

No indication recorded.