Have you had an

organ transplant?

Are you experiencing

skin cancers?

 

 

We have a unique study

opportunity designed

for organ transplant

recipients who have actinic

keratoses (pre-cancerous

rough skin patches) and a

history of frequent non-

melanoma skin cancers. 

 

 

Inclusion Criteria including:

§    Male or female at least 18 years of age.

§    Be an organ transplant (e.g., kidney, pancreas, liver, lungs, heart or combination) recipient outpatient taking immunosuppressive medication.

§    Females must be post-menopausal, surgically sterile or using a medically acceptable form of birth control with a negative urine pregnancy test at the first visit.

§    Provide written and verbal informed consent.

§    Have at least three (3) actinic keratosis lesions in near proximity to each other (either on the top of the forearms or bald scalp).

§    Have had two (2) non-melanoma skin cancers in the past 12 months (either on the top of the forearms or bald scalp).

§    Willing to follow study instructions and return to the clinic for required visits.

 

 

Exclusion Criteria including:

§    Pregnancy.

§    History of photosensitivity, or sensitivity to Levulan.

§    You are currently enrolled in another investigational drug/device study, or have been enrolled into such a study within 30 days prior to the initiation of this study.

§    You have used specific topical preparations on the selected treatment area (your doctor will discuss with you).

§    You have had systemic retinoid therapy within 6 months of the initiation of treatment.

 

 

 

 

We are seeking organ transplant recipients taking anti-rejection medication to participate in a study designed to test photodynamic therapy (PDT) to treat actinic keratoses (pre-cancerous rough skin patches).  The information gathered from this study will also assess the potential of PDT in the prevention of non-melanoma skin cancers.  Photodynamic therapy is the use of a topical solution and the application of a specialized light. 

 

If you meet the inclusion and exclusion criteria, the medical staff will go over your medical history with you, you will be asked to sign a consent form which explains the details of the study, you will be given a brief medical exam, as well as having a blood sample taken.  You will be enrolled into a treatment group receiving Levulan® (the topical solution) with photodynamic therapy or a treatment group receiving placebo topical solution with photodynamic therapy.

 

If you have been diagnosed with actinic keratoses and have a history of frequent non-melanoma skin cancers, please speak to your doctor about participating in this research study. 

 

Please give us a call today for more information about this important study.

(858) 571-1800 ext. 131

 

Email us at: jberg@therapeuticsinc.com

 

 

Study Sites in the following cities:

Boston, MA (Tufts); New York, NY (Mt. Sinai); Miami, FL (University of Miami; Nashville, TN (Vanderbilt); Philadelphia, PA (Fox Chase Cancer Center);
Irvine, CA (UCI); and San Francisco, CA (UCSF)

 

This research is sponsored by DUSA Pharmaceuticals, Inc