Clinical trial

Immunogenicity and Safety of a DTPa-HBV-IPV/Hib Vaccine Given at 2, 3 and 4…

NCT00376779 · GlaxoSmithKline, Industry · Completed

Key facts

NCT number NCT00376779
Title Immunogenicity and Safety of a DTPa-HBV-IPV/Hib Vaccine Given at 2, 3 and 4 Months of Age
Official title A Phase II, Observer-blind, Randomized Study to Evaluate the Immunogenicity, Safety and Reactogenicity of GlaxoSmithKline (GSK) Biologicals' Combined DssiTgdPa-HBV-IPV/Hib Vaccine Containing Diphtheria Toxoid From the Statens Serum Institute (SSI) of Denmark and Tetanus Toxoid From GSK Biologicals'…
Lead sponsor GlaxoSmithKline, Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Acellular Pertussis, Tetanus, Diphtheria, Hepatitis B, Poliomyelitis, Haemophilus Influenzae Type b
Intervention type Biological
Interventions Infanrix hexa Vaccine
Enrollment 450
Start date Oct 1, 2006
Primary completion May 1, 2007
Completion May 1, 2007
First posted Sep 15, 2006
Last update posted Nov 4, 2016
Countries Finland

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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