drugset / Trial / NCT00382187

Safety and Immunogenicity of Two Adjuvanted and One Non-adjuvanted H5N1 Influenza Vaccine in Adults

NCT00382187 ↗

Phase 2 Completed 40 enrolled Novartis Vaccines
RandomizedParallel-groupSingle-blindPrevention

Summary

The present study aims to evaluate safety and immunogenicity of two doses, administered three weeks apart, and a 6 month booster dose, of two influenza vaccines containing 7.5 micrograms or 15 micrograms of H5N1 influenza antigen, and of a non-adjuvanted influenza vaccine containing 15 micrograms of H5N1 influenza antigen, in adults

Timeline

Start
2006-11
Primary completion
2008-01
Completion
2008-01

Drugs

EvaluationDrugModalityDoseRoute
Subject MF59 adjuvanted H5N1 influenza vaccine Vaccine 7.5 ug —
Subject MF59 adjuvanted H5N1 influenza vaccine Vaccine 15 ug —
Subject non-adjuvanted influenza vaccine Vaccine 15 ug —

Indications