drugset / Trial / NCT01560793

Safety and Immunogenicity of a Novel H5N1 Influenza Vaccine in Healthy Adults Age 18-49 Years

NCT01560793 ↗

Phase 1 Completed 224 enrolled VaxInnate Corporation
NaSingle-groupTriple-blindPrevention

Summary

This study will evaluate the safety and immunogenicity of VAX161B \[STF2.HA5 H5N1\], a recombinant, inactivated, subunit influenza vaccine given as a two dose regimen at a range of doses.

Timeline

Start
2012-06
Primary completion
2013-06
Completion
2013-11

Drugs

EvaluationDrugModalityDoseRoute
Subject VAX161 Unknown 1 ug Intramuscular
Subject VAX161 Unknown 2.5 ug Intramuscular
Subject VAX161 Unknown 4 ug Intramuscular
Subject VAX161 Unknown 6 ug Intramuscular
Subject VAX161 Unknown 8 ug Intramuscular
Subject VAX161 Unknown 12 ug Intramuscular

Indications