drugset / Trial / NCT01612000

Safety and Immunogenicity of PanBlok Influenza Vaccine in Healthy Adults

NCT01612000 ↗

Phase 1/2 Completed 341 enrolled Protein Sciences Corporation
RandomizedParallel-groupQuadruple-blindPrevention

Summary

The purpose of this study is to investigate the safety and immunogenicity of a recombinant hemagglutinin (rHA) influenza vaccine derived from A/Indonesia/05/2005 (H5N1) administered at 3 dose levels in adjuvanted (SE) rHA formulations and 1 dose levels in an un-adjuvanted rHA formulation.

Timeline

Start
2012-05
Primary completion
2013-08
Completion
2013-12

Drugs

EvaluationDrugModalityDoseRoute
Subject PanBlok Vaccine 3.8 ug Intramuscular
Subject PanBlok Vaccine 7.5 ug Intramuscular
Subject PanBlok Vaccine 15 ug Intramuscular
Subject rHA adjuvant Unknown 2 % Intramuscular

Indications