drugset / Trial / NCT00677820

A Prospective Study to Evaluate the Safety of a New Trivalent Intranasal Influenza Vaccine

NCT00677820 ↗

Phase 4 Completed 300 enrolled MedImmune LLC
RandomizedParallel-groupQuadruple-blindPrevention

Summary

This prospective annual release study was designed to assess the safety of a trivalent influenza virus vaccine using a new strain recommended for the 2008-2009 influenza season not previously contained in the trivalent intranasal FluMist vaccine. Three hundred healthy adults received a single dose of vaccine or placebo and were followed for 180 days.

Timeline

Start
2008-06
Primary completion
2008-07
Completion
2008-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Trivalent Influenza Virus Vaccine Vaccine 0.5 ml Intranasal

Indications