Clinical trial

Human Papilloma Virus Vaccine Immunogenicity and Safety Trial in Young Adult…

NCT00231413 · GlaxoSmithKline, Industry · Completed

Key facts

NCT number NCT00231413
Title Human Papilloma Virus Vaccine Immunogenicity and Safety Trial in Young Adult Women With GSK Bio's Novel HPV Vaccine.
Official title A Dose-range Study to Assess the Safety and Immunogenicity of a Novel HPV Vaccine When Administered Intramuscularly According to a 3-dose Schedule (0,1,6-month) in Healthy Adult Females (18-25 Years of Age)
Lead sponsor GlaxoSmithKline, Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Infections, Papillomavirus
Intervention type Biological
Interventions HPV 16/18 L1 AS04, HPV-16/18/31/45 L1 AS04 Formulation 1, HPV-16/18/31/45 L1 AS04 Formulation 2, HPV-16/18/31/45 L1 AS04 Formulation 3, HPV-16/18/31/45 L1 AS04 Formulation 4, HPV-16/18/31/45 L1 AS04 Formulation 5, HPV-16/18/31/45 L1 AS04 Formulation 6
Enrollment 383
Start date Mar 4, 2005
Primary completion Mar 27, 2006
Completion Mar 27, 2006
First posted Oct 4, 2005
Last update posted Dec 12, 2019
Countries Belgium, 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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