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Completed Phase 3 Interventional Results available

Safety and Effectiveness Study of Imiquimod Creams for the Treatment of Actinic Keratoses (AKs)

ClinicalTrials.gov ID: NCT00603798

Public ClinicalTrials.gov record NCT00603798. 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 21, 2026, 10:09 PM 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-blinded, Placebo-controlled, Multicenter, Efficacy and Safety Study of Six Weeks of Treatment With Imiquimod Creams for Actinic Keratoses

Study identification

NCT ID
NCT00603798
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Graceway Pharmaceuticals, LLC
Industry
Enrollment
490 participants

Conditions and interventions

Interventions

  • Imiquimod cream Drug
  • Placebo cream Drug

Drug

Eligibility (public fields only)

Age range
18 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
Dec 31, 2007
Primary completion
Jun 30, 2008
Completion
Jun 30, 2008
Last update posted
Jun 28, 2010

2008

United States locations

U.S. sites
26
U.S. states
16
U.S. cities
25
Facility City State ZIP Site status
Not listed Birmingham Alabama 35205
Not listed Little Rock Arkansas 72205
Not listed Encino California 91436
Not listed Vista California 92083
Not listed New Britain Connecticut 06052
Not listed New Haven Connecticut 06511
Not listed Coral Gables Florida 33134
Not listed West Palm Beach Florida 33401
Not listed Arlington Heights Illinois 60005
Not listed Champaign Illinois 61820
Not listed Carmel Indiana 46032
Not listed Evansville Indiana 47713
Not listed South Bend Indiana 46617
Not listed Louisville Kentucky 40202
Not listed Omaha Nebraska 68144
Not listed Reno Nevada 89509
Not listed Albuquerque New Mexico 87106
Not listed Portland Oregon 97223
Not listed Philadelphia Pennsylvania 19034
Not listed Nashville Tennessee 37203
Not listed Dallas Texas 75246
Not listed Houston Texas 77030
Not listed Houston Texas 77058
Not listed San Antonio Texas 78229
Not listed Norfolk Virginia 23507
Not listed Woodbridge Virginia 22191

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 NCT00603798, 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 Jun 28, 2010 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00603798 live on ClinicalTrials.gov.

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