drugset / Trial / NCT04192500

Safety and Immune Response of One Dose of OVX836 at Two Dose Levels, in Comparison to Influvac TetraTM, After Intramuscular Administration in Healthy Subjects Aged 18-65 Years

NCT04192500

Phase 2 Completed 300 enrolled Osivax University Ghent · collab
RandomizedParallel-groupDouble-blindPrevention

Summary

This Phase 2a clinical study is designed to evaluate the immunogenicity and the safety of one dose of OVX836 influenza vaccine administered IM, confirm the dose level and regimen, and expand immunogenicity and safety data to adults through age 65.

Timeline

Start
2019-12-11
Primary completion
2020-09-07
Completion
2020-09-07

Drugs

EvaluationDrugModalityDoseRoute
Comparator Influvac TetraTM Vaccine Intramuscular
Subject OVX836 Vaccine 90 ug Intramuscular
Subject OVX836 Vaccine 180 ug Intramuscular

Indications