Clinical trial

Compare Immunogenicity & Safety of 2 Formulations of GSK Biologicals'…

NCT00320463 · GlaxoSmithKline, Industry · Completed

Key facts

NCT number NCT00320463
Title Compare Immunogenicity & Safety of 2 Formulations of GSK Biologicals' DTPa-HBV-IPV/Hib Vaccine Given in Healthy Infants
Official title Compare Immunogenicity & Reactogenicity of 2 Formulations of GSK Biologicals' DTPa-HBV-IPV/Hib Vaccine (New vs Current) Given in Healthy Infants. The DTPa-HBV-IPV Vaccine (New Formulation) Will Also be Assessed in a 3rd Group of Subjects
Lead sponsor GlaxoSmithKline, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Diphtheria, Hepatitis B, Poliomyelitis, Tetanus, Acellular Pertussis
Intervention type Biological
Interventions DTPa-HBV-IPV/Hib vaccine
Enrollment 415
Start date Apr 1, 2006
Completion Jan 1, 2007
First posted May 3, 2006
Last update posted Oct 12, 2016
Countries Russia

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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