Immunogenicity and Safety Study of GlaxoSmithKline Biologicals' GSK2202083A Vaccine Administered as a Booster Dose

PHASE2CompletedINTERVENTIONAL
Enrollment

391

Participants

Timeline

Start Date

August 18, 2010

Primary Completion Date

December 3, 2010

Study Completion Date

December 3, 2010

Conditions
TetanusDiphtheriaHaemophilus Influenzae Type bHepatitis BPoliomyelitisAcellular PertussisDiphtheria-Tetanus-aPertussis-Hepatitis B-Poliomyelitis-Haemophilus Influenzae Type b-Neisseria Meni
Interventions
BIOLOGICAL

GSK2202083A vaccine

Intramuscular, one dose.

BIOLOGICAL

Infanrix hexa™

Intramuscular, one dose.

BIOLOGICAL

Menjugate™

Intramuscular, one dose.

BIOLOGICAL

NeisVac-C™

Intramuscular, one dose.

BIOLOGICAL

Synflorix™

Intramuscular, one dose.

Trial Locations (9)

50345

GSK Investigational Site, Wroclaw

85-021

GSK Investigational Site, Bydgoszcz

39-200

GSK Investigational Site, Dębica

31-422

GSK Investigational Site, Krakow

31-503

GSK Investigational Site, Krakow

41-103

GSK Investigational Site, Siemianowice Śląskie

33-100

GSK Investigational Site, Tarnów

Unknown

GSK Investigational Site, Torun

55-100

GSK Investigational Site, Trzebnica

Sponsors

Lead Sponsor

All Listed Sponsors
lead

GlaxoSmithKline

INDUSTRY

NCT01171989 - Immunogenicity and Safety Study of GlaxoSmithKline Biologicals' GSK2202083A Vaccine Administered as a Booster Dose | Biotech Hunter | Biotech Hunter