drugset / Trial / NCT04146623

Safety Study of Live Attenuated Influenza Vaccine, CodaVax, Delivered Via Intranasal Spray

NCT04146623

Phase 1 Completed 33 enrolled Codagenix, Inc
RandomizedParallel-groupDouble-blindPrevention

Summary

This study is being conducted to assess the safety, tolerability, and immunogenicity of the live-attenuated CodaVax-H1N1 influenza vaccine as compared to normal saline placebo both administered via intranasal spray to healthy adults.

Timeline

Start
2019-05-07
Primary completion
2020-10-11
Completion
2020-11-11

Drugs

EvaluationDrugModalityDoseRoute
Subject CodaVax-H1N1 Vaccine 800000 unknown Intranasal

Indications