Clinical Trials Directory

Trials / Completed

CompletedNCT01184976

Study Of VGX-3400, H5N1 Avian Flu Virus Plasmid DNA With Electroporation Device In Healthy Adult Males

Phase I, Open-Label, Dose Escalation Study to Evaluate the Safety, Tolerability, and Immunogenicity in Healthy Adult Males of a DNA Plasmid Vaccine for HS Avian Influenza (VGX-3400) Administered by Intramuscular (IM) Injection Followed by Electroporation (EP)

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
30 (actual)
Sponsor
GeneOne Life Science, Inc. · Industry
Sex
Male
Age
20 Years – 39 Years
Healthy volunteers
Accepted

Summary

Research Hypothesis: VGX-3400 (DNA plasmids encoding the hemagglutinin (HA), neuraminidase (NA), and M2e-NP antigen of the H5N1 avian influenza virus) administered to healthy adult males by IM injection followed by EP will be generally well tolerated and immunogenic.

Conditions

Interventions

TypeNameDescription
BIOLOGICALVGX-3400Plasmid DNA delivered via IM injection with electroporation

Timeline

Start date
2010-08-01
Primary completion
2012-04-01
Completion
2012-04-01
First posted
2010-08-19
Last updated
2015-03-17

Locations

2 sites across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01184976. Inclusion in this directory is not an endorsement.

Study Of VGX-3400, H5N1 Avian Flu Virus Plasmid DNA With Electroporation Device In Healthy Adult Males (NCT01184976) · Clinical Trials Directory