Clinical trial

Study to Assess Safety & Immunogenicity of GSK Biologicals' DTPa/Hib Vaccine vs…

NCT00412854 · GlaxoSmithKline, Industry · Completed

Key facts

NCT number NCT00412854
Title Study to Assess Safety & Immunogenicity of GSK Biologicals' DTPa/Hib Vaccine vs Separate Administration of DTPa and Hib.
Official title Phase IIIb, Multicentre Study to Assess Safety & Immunogenicity of GSK Biologicals' Combined DTPa/Hib (Infanrix/Hib) Vaccine vs Separate Administration of DTPa (Infanrix) & Hib (Hiberix) Vaccines in Healthy Infants 3,4,&5 Months of Age as Compared With the Separate Administration of DTPa and Hib…
Lead sponsor GlaxoSmithKline, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Tetanus, Diphtheria, Acellular Pertussis
Intervention type Biological
Interventions Infanrix™/Hib, Infanrix, Hiberix
Enrollment 660
Start date Jan 3, 2007
Primary completion Jun 1, 2007
Completion Jun 25, 2007
First posted Dec 19, 2006
Last update posted Jun 6, 2018
Countries China

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.

About ClinicalTrials.gov studies

ClinicalTrials.gov is the U.S. National Library of Medicine's registry of clinical studies conducted around the world. Contact and investigator details are not shown here.

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

Browse all ClinicalTrials.gov studies