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Completed Phase 2 Interventional Results available

Safety of and Immune Response to the Human Papillomavirus (HPV) Vaccine in HIV-Infected Women

ClinicalTrials.gov ID: NCT00604175

Public ClinicalTrials.gov record NCT00604175. 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 Jul 22, 2026, 3:28 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 Phase II Study to Evaluate the Immunogenicity and Safety of a Quadrivalent Human Papillomavirus Vaccine in HIV-1-Infected Females

Study identification

NCT ID
NCT00604175
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
NIH
Enrollment
319 participants

Conditions and interventions

Interventions

  • Quadrivalent HPV vaccine Biological

Biological

Eligibility (public fields only)

Age range
13 Years to 45 Years
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

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

Study timeline

Start date
Jan 31, 2008
Primary completion
Dec 31, 2011
Completion
Oct 31, 2012
Last update posted
Nov 3, 2021

2008 – 2012

United States locations

U.S. sites
56
U.S. states
23
U.S. cities
40
Facility City State ZIP Site status
Alabama Therapeutics CRS Birmingham Alabama 35294-2050
Usc La Nichd Crs Alhambra California 90033
University of California, UC San Diego CRS La Jolla California 92093-0672
Miller Children's Hosp. Long Beach CA NICHD CRS Long Beach California 90806
University of Southern California CRS Los Angeles California 90033-1079
UCLA CARE Center CRS Los Angeles California 90035
Stanford AIDS Clinical Trials Unit CRS Palo Alto California 94304-5350
UCSD Antiviral Research Center CRS San Diego California 92103
Ucsf Hiv/Aids Crs San Francisco California 94110
University of Colorado Hospital CRS Aurora Colorado 80045
Denver Public Health CRS Denver Colorado 80204
Georgetown University CRS (GU CRS) Washington D.C. District of Columbia 20007
Howard Univ. Washington DC NICHD CRS Washington D.C. District of Columbia 20060
South Florida CDTC Ft Lauderdale NICHD CRS Fort Lauderdale Florida 33316
Univ. of Florida Jacksonville NICHD CRS Jacksonville Florida 32209
Pediatric Perinatal HIV Clinical Trials Unit CRS Miami Florida 33136
The University of Miami AIDS Clinical Research Unit (ACRU) CRS Miami Florida 33136
The Ponce de Leon Center CRS Atlanta Georgia 30308
Mt. Sinai Hosp. Med. Ctr. - Chicago, Womens & Childrens HIV Program Chicago Illinois 60608
Northwestern University CRS Chicago Illinois 60611
Rush Univ. Med. Ctr. ACTG CRS Chicago Illinois 60612
Rush University CRS Chicago Illinois 60612
Tulane Univ. New Orleans NICHD CRS New Orleans Louisiana 70112
IHV Baltimore Treatment CRS Baltimore Maryland 21201
Johns Hopkins University CRS Baltimore Maryland 21205
Massachusetts General Hospital CRS (MGH CRS) Boston Massachusetts 02114
Bmc Actg Crs Boston Massachusetts 02118
Beth Israel Deaconess Med. Ctr., ACTG CRS Boston Massachusetts 02215
Henry Ford Hosp. CRS Detroit Michigan 48202
Washington University Therapeutics (WT) CRS St Louis Missouri 63110-1010
Cooper Univ. Hosp. CRS Camden New Jersey 08103
New Jersey Medical School- Adult Clinical Research Ctr. CRS Newark New Jersey 07103
Weill Cornell Chelsea CRS New York New York 10011
NY Univ. HIV/AIDS CRS New York New York 10016
Columbia P&S CRS New York New York 10032-3732
Columbia IMPAACT CRS New York New York 10032
Trillium Health ACTG CRS Rochester New York 14607
Univ. of Rochester ACTG CRS Rochester New York 14642
Chapel Hill CRS Chapel Hill North Carolina 27599
Duke Univ. Med. Ctr. Adult CRS Durham North Carolina 27710
Greensboro CRS Greensboro North Carolina 27401
Cincinnati CRS Cincinnati Ohio 45219
Case CRS Cleveland Ohio 44106
MetroHealth CRS Cleveland Ohio 44109
Ohio State University CRS Columbus Ohio 43210
The Research & Education Group-Portland CRS Portland Oregon 97210
Penn Therapeutics, CRS Philadelphia Pennsylvania 19104
Thomas Jefferson Univ. Med. Ctr. CRS Philadelphia Pennsylvania 19107
University of Pittsburgh CRS Pittsburgh Pennsylvania 15213
The Miriam Hospital Clinical Research Site (TMH CRS) CRS Providence Rhode Island 02906
Vanderbilt Therapeutics (VT) CRS Nashville Tennessee 37204
Trinity Health and Wellness Center CRS Dallas Texas 75208
Texas Children's Hospital CRS Houston Texas 77030-2399
Houston AIDS Research Team CRS Houston Texas 77030
Virginia Commonwealth Univ. Medical Ctr. CRS Richmond Virginia 23298
University of Washington AIDS CRS Seattle Washington 98104-9929

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 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00604175, 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 Nov 3, 2021 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00604175 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →