Clinical Trials Directory

Trials / Terminated

TerminatedNCT00849069

Study to Assess the Safety of a New GSK Biologicals' GSK2231395A Candidate Vaccine

An Observer-blind, Safety Study of GSK Biologicals' Haemophilus Influenzae and Streptococcus Pneumoniae Candidate Vaccine in Adults.

Status
Terminated
Phase
Phase 1
Study type
Interventional
Enrollment
30 (estimated)
Sponsor
GlaxoSmithKline · Industry
Sex
All
Age
40 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the safety, reactogenicity and immunogenicity of GSK2231395A candidate vaccine in adults and elderly adults with chronic obstructive pulmonary disease. Subjects will be vaccinated 3 times with an interval of respectively 2 and 10 months.

Conditions

Interventions

TypeNameDescription
BIOLOGICALGSK2231395A3 doses intramuscular injections
BIOLOGICALTwinrixTM3 doses intramuscular injections

Timeline

Start date
2009-03-12
Primary completion
2009-04-07
Completion
2009-04-07
First posted
2009-02-23
Last updated
2017-10-31

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT00849069. Inclusion in this directory is not an endorsement.

Study to Assess the Safety of a New GSK Biologicals' GSK2231395A Candidate Vaccine (NCT00849069) · Clinical Trials Directory