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The U.S. Food and Drug Administration has granted approval to Scenesse (afamelanotide) to increase pain-free light exposure in adult patients with a history of phototoxic reactions (damage to skin) from erythropoietic protoporphyria.
Prior to this approval, there were no FDA-approved treatments to help erythropoietic protoporphyria patients increase their light exposure… (FDA, October 8, 2019)