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Completed Phase 3 Interventional Results available

Phase 3 Study of Imiquimod Creams in the Treatment of External Genital Warts

ClinicalTrials.gov ID: NCT00735462

Public ClinicalTrials.gov record NCT00735462. 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 21, 2026, 4:06 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 Safety and Effectiveness Study of Imiquimod Creams in the Treatment of External Genital Warts

Brief summary

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

The purpose of this study is to determine whether imiquimod creams are effective in treating external genital warts (EGW). The secondary objective of this study is to provide information on recurrence of EGW. Additionally the study will also look at any adverse events associated with the use of the creams. External genital and perianal warts are caused by the infection of human papillomavirus or HPV. HPV infection is a sexually transmitted disease (STD). External genital warts look like small flesh-colored, pink, or red growths on or around the external skin of sex organs or perianal area. The warts may look similar to the small parts of a cauliflower or they may be very tiny and difficult to see. They often appear in clusters of three or four, and may grow and spread rapidly. They usually are not painful, although they may cause mild pain, bleeding, and itching.

Study identification

NCT ID
NCT00735462
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Graceway Pharmaceuticals, LLC
Industry
Enrollment
511 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 Years and older
Sex
All
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
Aug 2008 (Type not available)
Primary completion
Jul 2009 (Actual)
Completion
Jul 2009 (Actual)
Last update posted
Jul 20, 2011

2008 – 2009

United States locations

U.S. sites
43
U.S. states
22
U.S. cities
38
Facility City State ZIP Site status
NEA Clinic Jonesboro Arkansas 72401 —
Northern Claifornia Research Carmichael California 95608 —
California State University - Chico Chico California 95929 —
Dermatology Research Associates Los Angeles California 90045 —
Conant Foundation San Francisco California 94114 —
Downtown Women's Healthcare Denver Colorado 80218 —
Altus Research Lake Worth Florida 33461 —
PMI Health Research Group Atlanta Georgia 30312 —
Atlanta Women's Research Institute Atlanta Georgia 30342 —
Altman Dermatology Associates Arlington Heights Illinois 61614 —
Howard Brown Chicago Illinois 60613 —
Valley Medical Center Flint Michigan 48507 —
Women's OB/GYN Saginaw Michigan 48604 —
Clayton Research Institute St Louis Missouri 63107 —
Women's Health Research Center Lawrenceville New Jersey 08648 —
Alliance Women's Research Riverside Park New Jersey 08075 —
Southwest Clinical Research Albuquerque New Mexico 87102 —
University Urology Associates New York New York 10016 —
Boro Park ObGyn New York New York 10121 —
Crescent Medical Research Salisbury North Carolina 28144 —
Piedmont Medical Research Winston-Salem North Carolina 27103 —
Rapid Medical Research Cleveland Ohio 44122 —
Complete Healthcare for Women Columbus Ohio 43213 —
Wright State University Dayton Ohio 45408 —
Heartland Health Institute Tulsa Oklahoma 74105 —
Clinical Trials of America Eugene Oregon 97401 —
Westover Heights Clinic Portland Oregon 97210 —
The Clinical Trial Center Jenkintown Pennsylvania 19046 —
Palmetto Clinical Research Greer South Carolina 29650 —
Alpha Clinical Research Clarksville Tennessee 37043 —
Adams Patterson Gynecology and Obstetrics Memphis Tennessee 38102 —
Tennessee Women's Care Nashville Tennessee 37203 —
DiscoveResearch Bryan Texas 77802 —
TMC Life Research Houston Texas 77054 —
West Houston Clinical Research Services Houston Texas 77055 —
Urology San Antonio Research San Antonio Texas 78229 —
The Center for Clinical Studies Webster Texas 77058 —
Utah Clinical Trials Salt Lake City Utah 84107 —
Wasatch Clinical Research Salt Lake City Utah 84107 —
CARE-ID Annandale Virginia 22003 —
Tidewater Clinical Reseach Virginia Beach Virginia 23456 —
Independence Family Medicine Clinical Research Virginia Beach Virginia 23513 —
Women's Clinical Research Center Seattle Washington 98105 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00735462, 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 Jul 20, 2011 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00735462 live on ClinicalTrials.gov.

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