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Trials / Completed

CompletedNCT00379977

Study to Assess the Safety & Reactogenicity of GSK Biologicals' DTPa/Hib Vaccine When Given at 3, 4 and 5 Months of Age

Open, Primary Vaccination Study to Assess Safety and Reactogenicity of GSK Biologicals' DTPa/Hib Vaccine When Administered to Healthy Chinese Infants at 3, 4 and 5 Months of Age.

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
30 (planned)
Sponsor
GlaxoSmithKline · Industry
Sex
All
Age
90 Days – 120 Days
Healthy volunteers
Accepted

Summary

This study will evaluate the safety and reactogenicity of GSK Biologicals' Diphtheria Tetanus acellular Pertussis/Haemophilus influenzae type b vaccine given to Chinese infants at 3, 4 and 5 months of age.

Conditions

Interventions

TypeNameDescription
BIOLOGICALdiphtheria, tetanus, pertussis & Hib vaccine

Timeline

Start date
2006-09-01
Completion
2006-12-01
First posted
2006-09-25
Last updated
2016-10-12

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT00379977. Inclusion in this directory is not an endorsement.

Study to Assess the Safety & Reactogenicity of GSK Biologicals' DTPa/Hib Vaccine When Given at 3, 4 and 5 Months of Age (NCT00379977) · Clinical Trials Directory