drugset / Trial / NCT00677820
A Prospective Study to Evaluate the Safety of a New Trivalent Intranasal Influenza Vaccine
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Trivalent Influenza Virus Vaccine | Vaccine | 0.5 ml | Intranasal |