drugset / Trial / NCT00424086

Safety and Immunogenicity Study of an Inactivated Influenza Vaccine (Split Virus, Vero Cell Derived)

NCT00424086 ↗

Phase 1/2 Completed 1000 enrolled Alachua Government Services, Inc.
RandomizedParallel-groupSingle-blindPrevention

Summary

The objective of this study is to assess the safety, tolerability and immunogenicity of a Split Virus, Vero Cell derived, Seasonal Influenza Vaccine (VCIV) in comparison to a Licensed Egg Derived, Split Virus, Seasonal Influenza Vaccine (EIV) in healthy subjects 18 years of age and older. Approximately 1000 subjects will be randomly assigned in a 3:1 ratio to receive a single injection of VCIV or EIV. Subjects will be monitored for 180 days following vaccination for occurrence of adverse reactions and for antibody response to the vaccine.

Timeline

Start
2007-01
Primary completion
—
Completion
2007-09

Drugs

EvaluationDrugModalityDoseRoute
Subject EIV Vaccine — —
Subject VCIV Vaccine — —

Indications