At a glance
ClinicalIndex Comparison RecordStandardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Immunogenicity and Safety of Multiple Formulations of an A/H1N1 Pandemic Vaccine in Healthy Adult and Elderly Subjects
In Brief
A Phase 2 clinical trial evaluating Monovalent Subvirion A/H1N1 Influenza vaccine (7.5 µg of HA), Monovalent Subvirion A/H1N1 Influenza vaccine (15 µg of HA), and 2 other interventions for Influenza and Swine-origin A/H1N1 Influenza. Completed, enrolled 849 participants across 15 sites.
Detailed Summary
The purpose of the study is to evaluate different doses of the Influenza A/H1N1 pandemic vaccine. Primary Objectives: * To describe the immunogenicity of the candidate vaccines after each injection. * To describe the safety of the candidate vaccines after each injection.
Study Details
Timeline
Interventions
0.5 mL, Intramuscular on Day 0 and on Day 21
0.5 mL, Intramuscular on Day 0 and Day 21
0.5 mL, Intramuscular on Day 0 and day 21
0.5 mL, Intramuscular on Day 0 and Day 21