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Completed Phase 3 Interventional Results available

Safety and Effectiveness Study of Imiquimod Creams in the Treatment of External Genital Warts

ClinicalTrials.gov ID: NCT00674739

Public ClinicalTrials.gov record NCT00674739. 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, 9:11 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 3, Randomized, Double-blind, Placebo-controlled, Multi-center, Efficacy and Safety 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
NCT00674739
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Graceway Pharmaceuticals, LLC
Industry
Enrollment
470 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
May 2008 (Type not available)
Primary completion
Jul 2009 (Actual)
Completion
Jul 2009 (Actual)
Last update posted
May 24, 2011

2008 – 2009

United States locations

U.S. sites
30
U.S. states
12
U.S. cities
28
Facility City State ZIP Site status
WILMAX Clinical Research Mobile Alabama 36608 —
Montgomery Women's Health Associates Montgomery Alabama 36116 —
Women's Health Research Phoenix Arizona 85015 —
Precision Trials Phoenix Arizona 85032 —
Premier Pharmaceutical Research Tempe Arizona 85282 —
Visions Clinical Research Tucson Arizona 85712 —
Edinger Medical Group Clinical Research Center Fountain Valley California 92708 —
East Bay Dermatology Medical Group Fremont California 94538 —
Coastal Medical Research Group San Luis Obispo California 93405 —
Torrance Clinical Research Torrance California 90505 —
Clinicos, LLC Colorado Springs Colorado 80904 —
Colorado Medical Research Center Denver Colorado 80210 —
Visions Clinical Research Boynton Beach Florida 33437 —
Segal Institute for Clinical Research North Miami Florida 33161 —
Miami Research Associates South Miami Florida 33143 —
Discovery Clinical Research Sunrise Florida 33316 —
Perimeter Institute for Clinical Research Atlanta Georgia 30338 —
Medical College of Georgia Augusta Georgia 30912 —
Atlanta North Gynecology Roswell Georgia 30075 —
Indiana University Infectious Disease Research Group Indianapolis Indiana 46202 —
Dermatology Practice Ann Arbor Michigan 48103 —
Alegent Health Clinic Omaha Nebraska 68124 —
Private Practice Great Neck New York 11021 —
Private Practice Purchase New York 10577 —
State University of NY Stony Brook Stony Brook New York 11794 —
Philadelphia Institute of Dermatology Philadelphia Pennsylvania 19144 —
Professional Quality Research, Women Partners in Health Austin Texas 78705 —
Professional Quality Research, The Urology Team Austin Texas 78759 —
University of Texas Southwestern Medical Center Dermatology Dept Dallas Texas 75390 —
Progressive Clinical Research San Antonio Texas 78229 —

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 NCT00674739, 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 May 24, 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 NCT00674739 live on ClinicalTrials.gov.

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