Carcinoma, Squamous Cell Clinical Trial
Official title:
A Multicentre, Randomised, Double-Blind, Placebo Controlled, Phase II Study to Evaluate the Safety and Efficacy of Subcutaneous Bioresorbable Implants of Afamelanotide (CUV1647) for the Prophylactic Treatment of Pre-Cancerous Skin Lesions of the Head, Forearms and Hands in Immune Compromised, Organ Transplant Patients.
The purpose of this study is to determine whether afamelanotide (CUV1647) is effective in
reducing the number of actinic keratoses and squamous cell carcinomas developing in immune
compromised organ transplant recipients, who are at particularly high risk, over a 24 month
test period.
The number of lesions formed on the head, hands and forarms will be monitored over this 24
month test period.
n/a
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Prevention
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