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Spots Global Cancer Trial Database for A Multi-center Study to Evaluate the Safety and Efficacy of PEP005 (Ingenol Mebutate) Gel, When Used to Treat Actinic Keratoses on Non-head Locations (Trunk and Extremities)

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Trial Identification

Brief Title: A Multi-center Study to Evaluate the Safety and Efficacy of PEP005 (Ingenol Mebutate) Gel, When Used to Treat Actinic Keratoses on Non-head Locations (Trunk and Extremities)

Official Title: A Multi-center, Open-label Study to Evaluate the Safety and Efficacy of PEP005 (Ingenol Mebutate) Gel, 0.05% in Patients With Actinic Keratoses on Non-head Locations (Trunk and Extremities)

Study ID: NCT00917306

Interventions

PEP005 Gel

Study Description

Brief Summary: The open label study is designed to assess the safety and efficacy of 0.05% PEP005 Gel when applied to an area of skin containing 4-8 AK lesions on non-head locations.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Park Avenue Dermatology, Orange Park, Florida, United States

Medaphase Inc, Newnan, Georgia, United States

Gwinnett Clinical Research Centre, Snellville, Georgia, United States

Michigan Center for Research Corp, Clinton Twp, Michigan, United States

Henry Ford Health Systems, Detroit, Michigan, United States

Dermatology Associates of Rochester, Rochester, New York, United States

Oregon Health and Science University, Portland, Oregon, United States

Dermatology Research Associates, Nashville, Tennessee, United States

Dematology on Ward, Adelaide, South Australia, Australia

Dermatology Institute of Victoria, Melbourne, Victoria, Australia

St John of God Dermatology, Subiaco, Western Australia, Australia

Contact Details

Name: Eugene Bauer, MD

Affiliation: Chief Medical Officer

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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