Clinical trial

Assess Immunogenicity, Reactogenicity, Safety of a Booster of GSK Biologicals…

NCT00332566 · GlaxoSmithKline, Industry · Completed

Key facts

NCT number NCT00332566
Title Assess Immunogenicity, Reactogenicity, Safety of a Booster of GSK Biologicals DTPw-HBV/Hib Kft Compared to DTPw-HBV/Hib
Official title Immunogenicity, Reactogenicity & Safety of a Booster Dose of GSK Biologicals' DTPw-HBV/Hib Kft Vaccine Vs GSK Biologicals' DTPw-HBV/Hib Vaccine, in Infants Who Received a 3-Dose Primary Vaccination Course With the Same Vaccines.
Lead sponsor GlaxoSmithKline, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Hepatitis B, Whole Cell Pertussis, Tetanus, Haemophilus Influenzae Type b, Diphtheria
Intervention type Biological
Interventions DTPw-HBV/Hib Kft vaccine GSK323527A, Tritanrix™-HepB/Hiberix™
Enrollment 148
Start date Jun 1, 2006
Primary completion Oct 1, 2006
Completion Oct 1, 2006
First posted Jun 1, 2006
Last update posted Sep 28, 2016
Countries Argentina, Nicaragua

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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