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Brief Title: The Safety Evaluation of the GSK-580299 Vaccine in Women From the Control Group in the Primary NCT00294047 Study
Official Title: Safety Study of GSK Biologicals' Human Papillomavirus Vaccine (GSK-580299) in Healthy Female Control Subjects From the Primary NCT00294047 Study
Study ID: NCT01249365
Brief Summary: This extension study is designed to assess the safety of GSK Biological's HPV vaccine GSK580299 in female subjects who took part in the primary study NCT00294047 and received the control vaccine in countries for which the licensed GSK HPV vaccine is not indicated for the subject's age group (26 years and older). This study is thus conducted to enable all women who received the control placebo in the primary NCT00294047 study to receive the GSK580299 vaccine.
Detailed Description: This Protocol Posting has been updated following Protocol Amendment 1, December 2010, leading to the update of 1 of the primary outcome measures and following Protocol Amendment 2, January 2011, leading to the removal of one of the exclusion criteria.
Minimum Age: 26 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: FEMALE
Healthy Volunteers: Yes
GSK Investigational Site, Parkville, Victoria, Australia
GSK Investigational Site, Perth, Western Australia, Australia
GSK Investigational Site, Almada, , Portugal
GSK Investigational Site, Coimbra, , Portugal
GSK Investigational Site, Lisboa, , Portugal
GSK Investigational Site, Porto, , Portugal
GSK Investigational Site, Setúbal, , Portugal
GSK Investigational Site, Ekaterinburg, , Russian Federation
GSK Investigational Site, Moscow, , Russian Federation
GSK Investigational Site, Moscow, , Russian Federation
GSK Investigational Site, Moscow, , Russian Federation
GSK Investigational Site, Sankt-Petersburg, , Russian Federation
GSK Investigational Site, Sankt-Petersburg, , Russian Federation
GSK Investigational Site, Singapore, , Singapore
GSK Investigational Site, Singapore, , Singapore
Name: GSK Clinical Trials
Affiliation: GlaxoSmithKline
Role: STUDY_DIRECTOR