SCENESSE® (afamelanotide 16mg)
The SCENESSE® (afamelanotide 16mg) Package Information Leaflet (English PDF) can be accessed here. The SCENESSE® (afamelanotide 16mg) Summary of Product Characteristics (English PDF) can be accessed here. Information in languages other than English available on the European Medicines Agency’s website here (external link).
SCENESSE® (INN: afamelanotide) is CLINUVEL’s proprietary first-in-class photoprotective drug. The drug has been approved for marketing authorisation under exceptional circumstances by the European Medicines Agency for the prevention of phototoxicity in adults with the orphan disease erythropoietic protoporphyria (EPP). In June 2018 CLINUVEL submitted a new drug application with the US FDA seeking marketing authorisation for SCENESSE®. Further studies of SCENESSE® are underway as a repigmentary agent in vitiligo.
In October 2018, CLINUVEL announced that a Phase IIa proof of concept study (CUV040) evaluating SCENESSE® in variegate porphyria (VP) is expected to start patient treatment in the northern hemisphere spring of 2019.
SCENESSE® (pronounced “sen-esse”) acts by increasing the levels of melanin in the skin; and shields against UV radiation (UVR) and sunlight. SCENESSE® is delivered via a subcutaneous dissolving implant approximately the size of a grain of rice. Increased pigmentation of the skin appears after two days and lasts up to two months.
Alpha-Melanocyte Stimulating Hormone (α-MSH) is a naturally occurring peptide hormone which is released by skin cells in response to the stimulation by ultraviolet radiation (UVR). α-MSH has a very short half-life (seconds) in the blood stream, sufficient to reach and stimulate other skin cells (melanocytes) which in turn produce and release melanin, a dark brown pigment. Melanin is known for its photoprotective effect.