Clinical trial

Evaluation of the Immunogenicity, Safety and Reactogenicity of the Combined…

NCT00290342 · GlaxoSmithKline, Industry · Completed

Key facts

NCT number NCT00290342
Title Evaluation of the Immunogenicity, Safety and Reactogenicity of the Combined DTPa-IPV Vaccine in Healthy Infants
Official title A Multicentric Study to Compare the Immunogenicity, Safety & Reactogenicity of GSK Biologicals' DTPa-IPV Vaccine vs. Co-administration of GSK's DTPa Vaccine & Sanofi-Pasteurs' IPV Vaccine at Different Injection Sites, to Healthy Children
Lead sponsor GlaxoSmithKline, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Tetanus, Acellular Pertussis, Diphtheria
Intervention type Biological
Interventions DTPa-IPV, DTPa, IMOVAX Polio®
Enrollment 458
Start date Jan 1, 2006
Primary completion Jan 1, 2007
Completion Jan 23, 2007
First posted Feb 13, 2006
Last update posted Oct 29, 2018
Countries South Korea

At a glance

  • 1–9 Study sites
  • Yes 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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