drugset / Trial / NCT01609998

Seasonal Influenza DNA Vaccine & Seasonal Influenza Trivalent Inactivated Vaccine (TIV) in Children & Adolescents

NCT01609998 ↗

RandomizedParallel-groupOpen-labelPrevention

Summary

This is a Phase I, dose escalation study in healthy adolescents and children (6-17 years) to evaluate the safety, tolerability, and immunogenicity of a prime-boost regimen of the 2012/2013 seasonal influenza DNA vaccine (HA DNA) followed by licensed 2012/2013 TIV vaccine. The comparator groups will receive licensed 2012/2013 TIV as prime and boost. The hypothesis is that the 2012/2013 HA DNA prime-TIV boost regimen will be safe and result in a broader and more durable immune response than is observed in age-matched comparator TIV-TIV groups.

Timeline

Start
2012-06
Primary completion
2013-07
Completion
2013-07

Drugs

EvaluationDrugModalityDoseRoute
Subject 2012/13 Seasonal Influenza Trivalent Inactivated Vaccine Vaccine — —
Subject Seasonal Influenza DNA vaccine Vaccine 1 mg Intramuscular
Subject Seasonal Influenza DNA vaccine Vaccine 4 mg Intramuscular

Indications