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Brief Title: 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
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-I)
Study ID: NCT00742391
Brief Summary: The purpose of this study is to determine whether topical application of PEP005 is effective for the treatment of actinic keratoses.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Omni Dermatology Research, Mesa, Arizona, United States
Colorado Medical Research Center, Denver, Colorado, United States
Advanced Dermatology and Cosmetic Research, Kissimmee, Florida, United States
Park Avenue Dermatology, Orange Park, Florida, United States
Advanced Dermatology & Cosmetic Surgery, Ormond Beach, Florida, United States
Medaphase Inc, Newnan, Georgia, United States
Gwinnett Clinical Research Centre, Snellville, Georgia, United States
Dermatology Center of Indiana/Indiana Clinical Trials Center, Plainfield, Indiana, United States
Henry Ford Health Systems, Detroit, Michigan, United States
Karen S. Harkaway, MD. LLC, South Delran, New Jersey, United States
Academic Dermatology Associates, Albuquerque, New Mexico, United States
Dermatology Associates of Rochester, Rochester, New York, United States
University Hospitals Case Medical Center, Cleveland, Ohio, United States
Oregon Medical Research, Portland, Oregon, United States
Oregon Health and Science University, Portland, Oregon, United States
Dermatology East, Germantown, Tennessee, United States
Rivergate Dermatology and Skin Care Center, Goodlettsville, Tennessee, United States
J & S Studies, Inc., College Station, Texas, United States
The Skin Centre, Benowa, Queensland, Australia
Burswood Dermatology, Victoria Park, Western Australia, Australia