drugset / Trial / NCT00311480

Safety and Immunogenicity of Two Doses, Administered Three Weeks Apart, of Two(Surface Antigen Adjuvanted With MF59C.1) Influenza Vaccines in Non-Elderly Adult and Elderly Subjects

NCT00311480 ↗

Phase 2 Completed 520 enrolled Novartis Novartis Vaccines · collab
RandomizedSingle-groupDouble-blindPrevention

Summary

The present study aims to evaluate safety and immunogenicity of two doses, administered three weeks apart, of two influenza vaccines containing 7.5 micrograms or 15 micrograms of H5N1 influenza antigen, in non-elderly adult and elderly subjects.

Timeline

Start
2006-03
Primary completion
—
Completion
—

Drugs

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

Indications