Clinical trial

Immuno & Safety Study With 2 Formulations of DTPw-HBV/HIB When Given at Birth…

NCT00316680 · GlaxoSmithKline, Industry · Terminated

Key facts

NCT number NCT00316680
Title Immuno & Safety Study With 2 Formulations of DTPw-HBV/HIB When Given at Birth With Hepatitis B at 2, 4 and 6 Mths.Age.
Official title Study to Assess Immunogenicity and Safety of GlaxoSmithKline Biologicals' Kft's DTPw-HBV/Hib vs DTPwCSL-HBV/Hib Kft and vs Concomitant Administration of CSL's Triple Antigen and GlaxoSmithKline Biologicals' Hiberix, to Infants at 2, 4, 6 Months of Age, After a Birth Dose of Hepatitis B
Lead sponsor GlaxoSmithKline, Industry
Status Terminated
Phase Phase 3
Study type Interventional
Conditions Haemophilus Influenzae Type b, Diphtheria, Tetanus, Hepatitis B, Whole Cell Pertussis
Intervention type Biological
Interventions Diphtheria, tetanus, pertussis, hepatitis B, Hib vaccine
Enrollment 288
Start date Mar 1, 2006
Completion Nov 1, 2006
First posted Apr 21, 2006
Last update posted Oct 7, 2016
Countries Dominican Republic

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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