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Study to Evaluate an Influenza Vaccine Candidate

NCT00321373 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 1220

Last updated 2018-06-08

Study results available
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Summary

The purpose of this study is to evaluate the immune response and safety of influenza vaccine candidate with or without adjuvant compared to Fluarix™ administered intramuscularly in elderly aged 60 years old and above.

Conditions

Interventions

BIOLOGICAL

Candidate Influenza Vaccine GSK1247446A - 2 different formulations

Single dose, Intramuscular injection

BIOLOGICAL

FluarixTM

Single dose, Intramuscular injection

Sponsors & Collaborators

Principal Investigators

  • GSK Clinical Trials · GlaxoSmithKline

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2006-05-11
Primary Completion
2006-07-01
Completion
2006-07-18

Countries

  • Finland
  • Greece

Study Locations

More Related Trials

Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00321373 on ClinicalTrials.gov