drugset / Trial / NCT00057330

HerpeVac Trial for Young Women

NCT00057330

Phase 3 Completed 8323 enrolled GlaxoSmithKline
RandomizedParallel-groupTriple-blindPrevention

Summary

The primary purpose of this study is to see if a herpes vaccine may prevent genital herpes disease in women who are not infected. The study will enroll approximately 7550 healthy women. These women will be randomly assigned to 1 of 2 possible study groups: herpes vaccine (experimental group) or hepatitis A vaccine (control group). Participants will receive their assigned vaccine at 0, 1, and 6 months. Participants will have 9 scheduled study visits and additional unscheduled visits for an evaluation of herpes if it is suspected. Participants will be involved in study related procedures for up to 20 months.

Timeline

Start
2003-01-14
Primary completion
2009-08-22
Completion
2009-08-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Havrix Vaccine 720 unknown Intramuscular
Subject SB208141 Vaccine 20 ug Intramuscular