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A Study to Evaluate the Safety, Immune Response, and Efficacy of an Investigational Vaccine in Women - Article


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Vaccine Safety and Adverse Event Reports

Clinical Trial: A Study to Evaluate the Safety, Immune Response, and Efficacy of an Investigational Vaccine in Women

This study is currently recruiting patients.

Sponsored by: Merck
Information provided by: Merck

Purpose

This study is to assess the tolerability and efficacy of a vaccine being evaluated to reduce the incidence of human papillomavirus (HPV) infection and disease (external genital warts and vulvar, vaginal, and cervical cancer) in women.

Condition Treatment or Intervention Phase
Healthy
Papillomavirus Infection
  Vaccine: Investigational Vaccine
 Phase II
Phase III

MedlinePlus related topics:  Viral Infections

Study Type: Interventional
Study Design: Prevention, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study

Eligibility

Ages Eligible for Study:  24 Years   -   45 Years,  Genders Eligible for Study:  Female

Accepts Healthy Volunteers

Criteria

  • No history of HPV infection, surgical treatment to the cervix, or gential warts

Location and Contact Information

Toll Free Number      1-888-577-8839 

Alabama
      Call for Information, Birmingham,  Alabama,  35233,  United States; No longer recruiting

California
      Call for Information, Davis,  California,  95616,  United States; No longer recruiting

      Call for Information, Colton,  California,  92324,  United States; No longer recruiting

      Call for Information, Fountain Valley,  California,  92708,  United States; No longer recruiting

Colorado
      Call for Information, Boulder,  Colorado,  80027,  United States; No longer recruiting

Florida
      Call for Information, Tampa,  Florida,  33607,  United States; No longer recruiting

Georgia
      Call for Information, Augusta,  Georgia,  30912,  United States; No longer recruiting

Illinois
      Call for Information, Champaign,  Illinois,  61820,  United States; No longer recruiting

Indiana
      Call for Information, Indianapolis,  Indiana,  46202-5124,  United States; No longer recruiting

Kentucky
      Call for Information, Bardstown,  Kentucky,  40004,  United States; No longer recruiting

New York
      Call for Information, Stony Brook,  New York,  11794-8091,  United States; No longer recruiting

North Carolina
      Call for Information, Chapel Hill,  North Carolina,  27514,  United States; No longer recruiting

Pennsylvania
      Call for International Site Information, Horsham,  Pennsylvania,  19044,  United States; Recruiting

      Call for Information, Trexlertown,  Pennsylvania,  18087-0060,  United States; No longer recruiting

      Call for Information, Philadelphia,  Pennsylvania,  19114,  United States; No longer recruiting

Virginia
      Call for Information, Richmond,  Virginia,  23226,  United States; No longer recruiting

More Information

Study ID Numbers:  2004_013
Record last reviewed:  March 2005
Last Updated:  March 21, 2005
Record first received:  August 25, 2004
ClinicalTrials.gov Identifier:  NCT00090220
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005


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October 13, 2008


Page Updated: November 22, 2004
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