drugset / Trial / NCT00161837

Comparison of the Safety and Immune Response of an Influenza Vaccine Made by a New Manufacturing Process With a Vaccine Made by the Traditional Manufacturing Process for Season 2003/2004

NCT00161837 ↗

Phase 2/3 Completed Alachua Government Services, Inc.
RandomizedParallel-groupSingle-blindPrevention

Summary

The objectives of the study are to assess the immunogenicity and safety of the inactivated influenza vaccine (whole virion, Vero cell-derived) at Day 21 and Day 180 after vaccination.

Timeline

Start
2003-12
Primary completion
—
Completion
2004-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Egg-derived Influenza Vaccine Vaccine — —
Subject Vero Cell-derived Influenza Vaccine Vaccine — —

Indications