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Description

Developed by the Australian company Clinuvel Pharmaceuticals under the commercial name Scenesse , afamelanotide received EMA approval in 2014 and FDA approval in 2019 for the prevention of phototoxicity in patients with erythropoietic protoporphyria (EPP), a rare orphan disease

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The regulatory landscape may evolve

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Special considerations : For patients taking tirzepatide (Mounjaro, Zepbound), note that it may reduce the effectiveness of oral contraceptives during initiation and dose escalation

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