Safety and Immunogenicity of Three Influenza Vaccines Adults Ages 18 and Older
Completed · Phase 3
Conditions studied: Influenza
In brief
Evaluate safety and immunogenicity of three influenza vaccines in adults 18 years of age and above.
Key facts
- Study ID
- NCT01992094
- Run by
- Novartis Vaccines
- People needed
- 2680
- Starts
- 2013-11-01
- Expected to finish
- 2014-07-01
- Last updated by the study team
- 2015-12-10
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Male or female ages 18 years and older.
- Individuals who give written informed consent, who can comply with study procedures, and who are available for follow-up.
You may not qualify if…
- Individuals recently vaccinated against influenza
- Subjects with contraindications to receive influenza vaccine
- Please contact the site for additional eligibility criteria
Where it is running
- Study site — Huntsville, Alabama, United States
- Study site — Phoenix, Arizona, United States
- Study site — Anaheim, California, United States
- Study site — San Diego, California, United States
- Study site — Coral Gables, Florida, United States
- Study site — Hollywood, Florida, United States
- Study site — Melbourne, Florida, United States
- Study site — South Miami, Florida, United States
- Study site — West Palm Beach, Florida, United States
- Study site — Peoria, Illinois, United States
- Study site — Mishawaka, Indiana, United States
- Study site — Council Bluffs, Iowa, United States
- Study site — Newton, Kansas, United States
- Study site — Wichita, Kansas, United States
- Study site — Wichita, Kansas, United States
- Study site — Metairie, Louisiana, United States
- Study site — Rockville, Maryland, United States
- Study site — Edina, Minnesota, United States
- Study site — Bellevue, Nebraska, United States
- Study site — Omaha, Nebraska, United States
- Study site — Endwell, New York, United States
- Study site — Rochester, New York, United States
- Study site — Cary, North Carolina, United States
- Study site — Charlotte, North Carolina, United States
- Study site — Raleigh, North Carolina, United States
Full record on ClinicalTrials.gov
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