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The regulatory picture is unusual and worth stating plainly: the afamelanotide molecule is FDA-approved but only as SCENESSE, a 16 mg controlled-release bioresorbable implant placed by a trained clinician to reduce phototoxic pain in adults with erythropoietic protoporphyria (EPP), a rare light-sensitivity disorder [1]

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In contrast, synthetic HGH acts downstream

MDL 3094 has been filed against Ozempic, Wegovy, and Rybelsus manufacturer Novo Nordisk as well as Trulicity and Mounjaro manufacturer Eli Lilly and Company