At a glance
ClinicalIndex Comparison RecordPhase 2Completed· 300 enrolled
Drug / intervention
Fluarix™ +1 morebiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Study to Evaluate the Immunogenicity, Safety and Reactogenicity of Adjuvanted Influenza Vaccine Candidates Compared to Fluarix™ Administered Intramuscularly in Subjects Aged 18-59 Years.
In Brief
A Phase 2 clinical trial evaluating Fluarix™ and GSK1247446A for Influenza. Completed, enrolled 300 participants across 1 site.
Detailed Summary
The purpose of this study is to evaluate the immunogenicity and the safety of candidate vaccines compared to Fluarix™ administered intramuscularly in subjects aged 18-59 years
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsInfluenza
CountriesBelgium
Collaborators--
Timeline
Phase 2CompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedSep 2006
Enrollment StartOct 2006
Primary CompletionNov 2006
Study CompletionNov 2006
TodayJul 2026
First PostedSep 12, 2006
Enrollment StartOct 3, 2006
Primary CompletionNov 1, 2006
Study CompletionNov 30, 2006
TodayJul 2, 2026
Enrollment to primary: 28 daysPosted 19.8 years ago
Interventions
Fluarix™biological
GlaxoSmithKline Biologicals' licensed influenza vaccine
GSK1247446Abiological
Low-dose GlaxoSmithKline Biologicals' GSK1247446A influenza vaccine