Clinical trial

Human Papilloma Virus Vaccine Safety and Immunogenicity Trial in Young…

NCT00196924 · GlaxoSmithKline, Industry · Completed

Key facts

NCT number NCT00196924
Title Human Papilloma Virus Vaccine Safety and Immunogenicity Trial in Young Adolescent Women With GSK Bio HPV-16/18.
Official title Evaluate the Safety and Immunogenicity of GSK Biologicals' HPV-16/18 Vaccine Administered Intramuscularly According to a 0,1,6 Month Schedule in Healthy Female Subjects (10 - 14 Years)
Lead sponsor GlaxoSmithKline, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Infections, Papillomavirus
Intervention type Biological
Interventions HPV-16/18 L1/AS04
Enrollment 2,067
Start date Jun 1, 2004
Primary completion Mar 1, 2006
Completion Mar 1, 2006
First posted Sep 20, 2005
Last update posted Mar 23, 2017
Countries Australia, Colombia, Czechia, France, Germany, Honduras, Norway, Panama, South Korea, Spain, Sweden, Taiwan

At a glance

  • 10–99 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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