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Peptide library / Skin & aging / Afamelanotide

FDA-approvedSkin & aging

Afamelanotide

An alpha-MSH analog implant that lets people with a rare light-sensitivity disease tolerate sun.

Body system
Skin & aging
Status
FDA-approved
Strongest evidence
FDA approved
Also known as
Scenesse, Melanotan I

Effects studied or claimed

What it is used or promoted for, and where each effect has actually been seen

  • Painful phototoxicity in erythropoietic protoporphyriaFDA approved
  • Vitiligo, studiedSmall human studies

How it is thought to work

Afamelanotide activates the melanocortin 1 receptor, increasing protective melanin in the skin without UV exposure.

What the evidence shows

Phase 3 trials showed more pain-free time in sunlight for adults with erythropoietic protoporphyria compared with placebo.

Safety and unknowns

Nausea, headache and darkening of moles and freckles. Skin should be checked regularly.

Regulatory status

FDA-approved as Scenesse in 2019 for erythropoietic protoporphyria only.

Regulatory status changes quickly. This entry was last reviewed on 27 October 2026. Confirm current status with the FDA before relying on it.

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General information, not medical advice. Do not buy or inject unregulated peptides.