Clinical trial

Long Term F/U Studies at Y5&6 to Demonstrate the Equivalence of 2 Vaccination…

NCT00197171 · GlaxoSmithKline, Industry · Completed

Key facts

NCT number NCT00197171
Title Long Term F/U Studies at Y5&6 to Demonstrate the Equivalence of 2 Vaccination Schedules of Combined Hepatitis A & B Vaccine
Official title Evaluate the Persistence of Immune Response of GSK Biologicals' TWINRIX™ ADULT, Administered According to 0,6 Month Schedule and 0,12 Month Schedule, in Volunteers Aged 12-15 Years Inclusive at the Time of First Vaccine Dose
Lead sponsor GlaxoSmithKline, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Hepatitis B, Hepatitis A
Intervention type Biological
Interventions Combined Hepatitis A and B vaccine
Enrollment 143
Start date Sep 1, 2003
Primary completion Dec 1, 2003
Completion Dec 1, 2003
First posted Sep 20, 2005
Last update posted Sep 7, 2016
Countries Australia

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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