Skip to content

Melanotan I

An FDA-approved selective MC1R agonist for erythropoietic protoporphyria (EPP). Stimulates protective eumelanin production without the broad side effects of Melanotan II.

StrongWell-Studied

What is Melanotan I?

Melanotan I (afamelanotide, brand name Scenesse) is a synthetic 13-amino-acid analog of alpha-melanocyte-stimulating hormone (alpha-MSH). It is FDA-approved (2019) and EMA-approved (2014) for the prevention of phototoxicity in adults with erythropoietic protoporphyria (EPP), a rare genetic condition that causes severe pain upon sun exposure. Unlike Melanotan II, afamelanotide is highly selective for the MC1R receptor, meaning it primarily stimulates skin pigmentation with minimal effects on sexual function, appetite, or cardiovascular parameters. It is administered as a subcutaneous implant by a healthcare provider every 60 days.

Why People Talk About It

Photoprotection for erythropoietic protoporphyria (FDA-approved)

Strong

Vitiligo repigmentation (combined with phototherapy)

Moderate

UV-free tanning and photoprotection

Emerging

DNA repair enhancement in skin

Emerging

Neuroprotection in acute stroke

Preliminary

How It Works

Melanotan I mimics the body's natural tanning hormone (alpha-MSH) but is much more potent and longer-lasting. It activates the MC1R receptor on melanocytes, stimulating them to produce eumelanin — the dark, protective pigment that shields DNA from UV damage. Unlike Melanotan II, it is highly selective for this one receptor, so it primarily affects pigmentation without significant effects on sexual function or appetite.

Common Questions

Safety Information

Important Safety Notes

Common Side Effects

Implant site reaction/discoloration (21%)Nausea (19%)Oropharyngeal pain (7%)Fatigue (6%)HeadacheSkin darkening (expected pharmacological effect)

Cautions

  • Only available as a healthcare-provider-administered implant
  • Not approved for cosmetic tanning
  • Darkening of existing moles has been reported in a small number of patients
  • Should be used under medical supervision for approved indications

What We Don't Know

Very long-term effects beyond 8 years of use are still being characterized. Effects on melanoma risk require ongoing surveillance, though no signal has emerged in post-marketing data. Optimal treatment duration and long-term discontinuation effects are being studied.

Published Research

12 studies

Afamelanotide for Erythropoietic Protoporphyria

Randomized Controlled TrialPMID: 26132941

German Cohort Observational Study to Investigate the Short- and Long-Term Safety and Clinical Effectiveness of Afamelanotide 16 mg (SCENESSE) in Patients With Erythropoietic Protoporphyria (EPP)

Observational StudyPMID: 40082741

Afamelanotide for Treatment of the Protoporphyrias: Impact on Quality of Life and Laboratory Parameters in a US Cohort

Observational StudyPMID: 38929673

Afamelanotide in protoporphyria and other skin diseases: a review

ReviewPMID: 38784937

A feasibility and safety study of afamelanotide in acute stroke patients — an open label, proof of concept, phase IIa clinical trial

Clinical TrialPMID: 37496004

Afamelanotide Is Associated with Dose-Dependent Protective Effect from Liver Damage Related to Erythropoietic Protoporphyria

Observational StudyPMID: 37109595

Into the Light: Afamelanotide and the Treatment of Erythropoietic Protoporphyria in the United States

ReviewPMID: 37683058

Afamelanotide: An Orphan Drug with Potential for Broad Dermatologic Applications

ReviewPMID: 33683075

Afamelanotide for prevention of phototoxicity in erythropoietic protoporphyria

ReviewPMID: 33507118

Association of Afamelanotide With Improved Outcomes in Patients With Erythropoietic Protoporphyria in Clinical Practice

Observational StudyPMID: 32186677

Increased phototoxic burn tolerance time and quality of life in patients with erythropoietic protoporphyria treated with afamelanotide — a three years observational study

Observational StudyPMID: 32811524

Afamelanotide and narrowband UV-B phototherapy for the treatment of vitiligo: a randomized multicenter trial

Randomized Controlled TrialPMID: 25230094

Related Peptides

Quick Facts

Class
Melanocortin Agonist
Evidence
Strong
Safety
Well-Studied
Updated
Apr 2026
Citations
12PubMed

Also known as

AfamelanotideScenesseMT-IMT-1NDP-MSHCUV1647

Tags

SkinPhotoprotectionFDA-ApprovedMelanocortinRare Disease

Evidence Score

Overall Confidence92%

Clinical Trials

View Clinical Trials

Links to ClinicalTrials.gov for reference. Listing does not imply endorsement.