Clinical trial

Immunogenicity and Safety of Havrix™ Co-Administered With a Diphtheria, Tetanus…

NCT00197236 · GlaxoSmithKline, Industry · Completed

Key facts

NCT number NCT00197236
Title Immunogenicity and Safety of Havrix™ Co-Administered With a Diphtheria, Tetanus and Pertussis and a Haemophilus b Vaccine in Children Aged 15 Months
Official title Immunogenicity and Safety of GSK Biologicals' Inactivated Hepatitis A Vaccine (Havrix™) Co-administered With GSK Biologicals' DTaP Vaccine (Infanrix™) and Aventis Pasteur's Haemophilus b Conjugate Vaccine (ActHIB) in Healthy Children 15 Months of Age
Lead sponsor GlaxoSmithKline, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Hepatitis A
Intervention type Biological
Interventions Havrix™, Infanrix™, ActHIB™
Enrollment 468
Start date Nov 11, 2003
Primary completion Dec 3, 2007
Completion Dec 3, 2007
First posted Sep 20, 2005
Last update posted Aug 20, 2018
Countries United States

At a glance

  • 10–99 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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