Trial Profile
A Phase III, Double-blind, Randomized, Controlled Study to Evaluate Immunogenicity and Safety of GSK Biologicals' HPV-16/18 L1 VLP AS04 Vaccine, Administered Intramuscularly (0, 1, 6 Month Schedule) in Healthy Females Aged 18 - 35 Years
Status:
Completed
Phase of Trial:
Phase III
Latest Information Update: 08 Sep 2023
Price :
$35
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At a glance
- Drugs Human papillomavirus vaccine recombinant bivalent Japan Vaccine/MedImmune (Primary)
- Indications Cervical cancer; Human papillomavirus infections
- Focus Pharmacodynamics; Registrational
- Sponsors GlaxoSmithKline; GSK
- 12 Dec 2007 Status changed from in progress to completed.
- 14 Nov 2006 Status change
- 25 Oct 2006 New trial record.