Clinical trial

Complementary Testing to Evaluate Immunogenicity of Human Papillomavirus (HPV)…

NCT00456807 · GlaxoSmithKline, Industry · Completed

Key facts

NCT number NCT00456807
Title Complementary Testing to Evaluate Immunogenicity of Human Papillomavirus (HPV) Vaccine (580299) in Healthy Female Subjects Aged >/= 26 Years
Official title Complementary Testing to Further Evaluate the Immunogenicity of a GSK Biologicals' HPV Vaccine (580299) in Healthy Female Subjects Aged Over 26 Years Enrolled in Study 104820.
Lead sponsor GlaxoSmithKline, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Infections, Papillomavirus
Intervention type Biological
Interventions Placebo, Cervarix TM
Enrollment 100
Start date Apr 1, 2007
Primary completion Jan 1, 2008
Completion Jan 1, 2008
First posted Apr 5, 2007
Last update posted Dec 16, 2016
Countries Netherlands

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.

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

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