Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional Accepts healthy volunteers Results available

HerpeVac Trial for Young Women

ClinicalTrials.gov ID: NCT00057330

Public ClinicalTrials.gov record NCT00057330. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 24, 2026, 7:22 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Double-Blind, Randomized, Controlled Phase III Study to Assess the Prophylactic Efficacy and Safety of gD-Alum/MPL Vaccine in the Prevention of Genital Herpes Disease in Young Women Who Are HSV-1 and -2 Seronegative

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT00057330
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
8,323 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 30 Years
Sex
Female
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 14, 2003 (Type not available)
Primary completion
Aug 22, 2009 (Actual)
Completion
Aug 22, 2009 (Actual)
Last update posted
Aug 27, 2018

2003 – 2009

United States locations

U.S. sites
67
U.S. states
28
U.S. cities
59
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35294 —
GSK Investigational Site Chandler Arizona 85224 —
GSK Investigational Site Mesa Arizona 85203 —
GSK Investigational Site Mesa Arizona 85213 —
GSK Investigational Site Phoenix Arizona 85014 —
GSK Investigational Site Phoenix Arizona 85032 —
GSK Investigational Site Tempe Arizona 85283 —
GSK Investigational Site Carson California 90747 —
GSK Investigational Site Long Beach California 90840 —
GSK Investigational Site Los Angeles California 90048 —
GSK Investigational Site San Diego California 92108 —
GSK Investigational Site San Diego California 92182 —
GSK Investigational Site San Francisco California 94115 —
GSK Investigational Site Torrance California 90502 —
GSK Investigational Site Vallejo California 94589 —
GSK Investigational Site Aurora Colorado 80045 —
GSK Investigational Site Athens Georgia 30602 —
GSK Investigational Site Atlanta Georgia 30322 —
GSK Investigational Site Augusta Georgia 30912-3500 —
GSK Investigational Site Satesboro Georgia 30460 —
GSK Investigational Site Chicago Illinois 60612-7323 —
GSK Investigational Site Bloomington Indiana 47405 —
GSK Investigational Site Indianapolis Indiana 46202 —
GSK Investigational Site Iowa City Iowa 52242 —
GSK Investigational Site Arkansas City Kansas 67005 —
GSK Investigational Site Newton Kansas 67114 —
GSK Investigational Site Wichita Kansas 67205 —
GSK Investigational Site Wichita Kansas 67207 —
GSK Investigational Site Bardstown Kentucky 40004 —
GSK Investigational Site Lexington Kentucky 40536 —
GSK Investigational Site Louisville Kentucky 40202 —
GSK Investigational Site Baton Rouge Louisiana 70808 —
GSK Investigational Site New Orleans Louisiana 70112 —
GSK Investigational Site Baltimore Maryland 21201 —
GSK Investigational Site Baltimore Maryland 21224 —
GSK Investigational Site College Park Maryland 20742 —
GSK Investigational Site Boston Massachusetts 02118 —
GSK Investigational Site St Louis Missouri 63104 —
GSK Investigational Site Omaha Nebraska 68134 —
GSK Investigational Site Albuquerque New Mexico 87131-0001 —
GSK Investigational Site Brooklyn New York 11201 —
GSK Investigational Site Brooklyn New York 11203 —
GSK Investigational Site New York New York 10029 —
GSK Investigational Site Rochester New York 14620 —
GSK Investigational Site Rochester New York 14642 —
GSK Investigational Site Stony Brook New York 11794-8091 —
GSK Investigational Site The Bronx New York 10461 —
GSK Investigational Site Chapel Hill North Carolina 27599 —
GSK Investigational Site Raleigh North Carolina 27607 —
GSK Investigational Site Cincinnati Ohio 45229 —
GSK Investigational Site Tulsa Oklahoma 74105 —
GSK Investigational Site Portland Oregon 97210 —
GSK Investigational Site Greenville Pennsylvania 16125 —
GSK Investigational Site Grove City Pennsylvania 16127 —
GSK Investigational Site Johnstown Pennsylvania 15904 —
GSK Investigational Site Monongahela Pennsylvania 15063 —
GSK Investigational Site Pittsburgh Pennsylvania 15241 —
GSK Investigational Site Wexford Pennsylvania 15090 —
GSK Investigational Site Kingston Rhode Island 02881 —
GSK Investigational Site Nashville Tennessee 37232 —
GSK Investigational Site Austin Texas 78705 —
GSK Investigational Site Houston Texas 77030 —
GSK Investigational Site Webster Texas 77598 —
GSK Investigational Site Salt Lake City Utah 84119 —
GSK Investigational Site Salt Lake City Utah 84132-2405 —
GSK Investigational Site Seattle Washington 98104 —
GSK Investigational Site La Crosse Wisconsin 54601 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 8 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00057330, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 27, 2018 · Synced Oct 24, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00057330 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →