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Completed Phase 3 Interventional Results available

A Multicenter Study to Evaluate the Efficacy and Safety of PEP005 (Ingenol Mebutate) Gel When Used to Treat Actinic Keratoses (AKs) on the Non Head Locations

ClinicalTrials.gov ID: NCT00942604

Public ClinicalTrials.gov record NCT00942604. 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 Sep 4, 2026, 10:08 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 Multi-center, Randomized, Parallel Group, Double-blind, Vehicle-controlled Study to Evaluate the Efficacy and Safety of PEP005 (Ingenol Mebutate) Gel, 0.05%, In Patients With Actinic Keratoses on Non-head Locations (REGION-Ib)

Brief summary

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

The purpose of this study is to determine whether topical application of PEP005 is effective for the treatment of actinic keratoses.

Study identification

NCT ID
NCT00942604
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Peplin
Industry
Enrollment
203 participants

Conditions and interventions

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
Jun 30, 2009
Primary completion
Sep 30, 2009
Completion
Sep 30, 2009
Last update posted
Mar 5, 2015

2009

United States locations

U.S. sites
17
U.S. states
11
U.S. cities
17
Facility City State ZIP Site status
Burke Pharmaceutical Research Hot Springs Arizona 71913
Skin Surgery Medical Group Inc. San Diego California 92117
Atlanta Dermatology, Vein & Research Center, LLC Alpharetta Georgia 30022
Altman Dermatology Associates Arlington Heights Illinois 60005
Glazer Dermatology Buffalo Grove Illinois 60089
Deaconess Clinic Downtown Evansville Indiana 47713
Dawes Fretzin Clinical Research Group, LLC Indianapolis Indiana 46256
Skin Specialists, PC Omaha Nebraska 68144
Karl G. Heine Dermatology Henderson Nevada 89002
Group Health Associates Cincinnati Ohio 45220
DermResearch, Inc. Austin Texas 78759
Suzanne Bruce and Associates, PA, The Center for Skin Research Houston Texas 77056
Dermatology Clinical Research Center of San Antonio San Antonio Texas 78229
Dermatology Associates of Tyler Tyler Texas 75703
Dermatology Research Center, Inc. Salt Lake City Utah 84124
The Education and Research Foundation Lynchburg Virginia 24501
Virginia Clinical Research, Inc Norfolk Virginia 23507

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 NCT00942604, 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 Mar 5, 2015 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00942604 live on ClinicalTrials.gov.

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