Melanotan I
Also known as: Afamelanotide, Scenesse, MT-1, CUV1647
Key Facts: Melanotan I
- Category
- Skin & Hair
- FDA Status
- FDA Approved
- Clinical Status
- FDA Approved (2019) - Erythropoietic Protoporphyria
- Administration
- Subcutaneous implant (not injection)
- Typical Dose
- 500-1000 mcg daily (loading), then 500-1000 mcg 1-2x weekly (maintenance)
- Frequency
- Daily during loading (1-2 weeks), then 1-2x weekly maintenance
- Duration
- Long-term / as needed before sun season
Mechanism of Action
Afamelanotide binds and activates the melanocortin-1 receptor (MC1R) on pigment-producing melanocytes, driving production of eumelanin, the dark, photoprotective form of melanin. Two amino acid swaps from natural alpha-MSH - norleucine at position 4 and D-phenylalanine at position 7 - make it bind MC1R more tightly and resist breakdown, so it lasts far longer and acts more potently than the native hormone. The extra eumelanin absorbs and scatters light and also brings antioxidant and DNA-repair-supporting effects, which is why it raises the light dose EPP patients can tolerate before pain hits. Unlike Melanotan II, it is selective enough toward MC1R that it is not primarily a sexual-function or appetite agent.
Research Summary
This is one of the few peptides on this list with gold-standard human evidence. The pivotal data came from two multicenter, randomized, double-blind, placebo-controlled trials published in the New England Journal of Medicine in 2015 (Langendonk et al., 373(1):48-59), enrolling 168 EPP patients across the EU and US who received the 16 mg implant or placebo every 60 days. Afamelanotide significantly increased pain-free time in sunlight (for example, median 69.4 vs 40.8 hours in the US trial), reduced phototoxic reactions, and improved disease-specific quality of life, with mostly mild adverse events. Long-term observational follow-up of EPP patients has supported continued benefit and an acceptable safety profile. The big caveats: this approval is narrowly for EPP, not for cosmetic tanning, and the unregulated injectable 'Melanotan' products people buy online are not the same controlled, clinician-administered implant and carry real risks. Bottom line: a genuinely proven, approved drug for a rare condition, frequently misused outside that lane.
Dosing Information
Typical Dosingⓘ
Community experience
500-1000 mcg daily (loading), then 500-1000 mcg 1-2x weekly (maintenance)
250-1000 mcg per injection
Daily during loading (1-2 weeks), then 1-2x weekly maintenance
Injected subcutaneously like MT-II. More selective than MT-II with fewer sexual side effects. Slower onset of tanning than MT-II. FDA version (Scenesse) is an implant for EPP patients only.
Research Dosingⓘ
Scientific studies
FDA-approved dosing for EPP
Doses from Studies
16 mg subcutaneous implant
Duration
Long-term / as needed before sun season
Administration
Subcutaneous implant (not injection)
Timing & Administration
Best Time to Take
Evening or before sun exposure
Daily during loading, then maintenance doses
Food Recommendation
With or without food
Why This Timing?
Similar to MT-II, evening use minimizes visible flushing. Pre-sun exposure maximizes tanning effect.
Possible Side Effects
Not everyone experiences these effects. Individual responses vary based on dosage, duration, and personal factors.
- ●Nausea (common)
- ●Skin darkening (intended effect)
- ●Headache
- ●Fatigue
- ●Injection site reactions
- ●FDA approved with known safety profile
References
- https://www.nejm.org/doi/full/10.1056/NEJMoa1411481
- https://pmc.ncbi.nlm.nih.gov/articles/PMC4780255/
- https://en.wikipedia.org/wiki/Afamelanotide
- https://dermnetnz.org/topics/afamelanotide
- https://pubmed.ncbi.nlm.nih.gov/25494545/
Research This Peptide Further
Frequently Asked Questions
What does Melanotan I do?
Melanotan I is the research name for afamelanotide, a 13-amino-acid synthetic analog of alpha-melanocyte-stimulating hormone (alpha-MSH), also written as [Nle4, D-Phe7]-alpha-MSH or NDP-MSH. It is the only melanocortin peptide with regulatory approval: sold as Scenesse, it was approved by the EMA in 2014 and the FDA in 2019 to increase pain-free light exposure in adults with erythropoietic protoporphyria (EPP). It is given as a 16 mg bioresorbable implant under the skin by a clinician, not as a tanning shortcut.
How does Melanotan I work?
Afamelanotide binds and activates the melanocortin-1 receptor (MC1R) on pigment-producing melanocytes, driving production of eumelanin, the dark, photoprotective form of melanin. Two amino acid swaps from natural alpha-MSH - norleucine at position 4 and D-phenylalanine at position 7 - make it bind MC1R more tightly and resist breakdown, so it lasts far longer and acts more potently than the native hormone. The extra eumelanin absorbs and scatters light and also brings antioxidant and DNA-repair-supporting effects, which is why it raises the light dose EPP patients can tolerate before pain hits. Unlike Melanotan II, it is selective enough toward MC1R that it is not primarily a sexual-function or appetite agent.
Is Melanotan I FDA approved?
Yes, Melanotan I is FDA approved. FDA Approved (2019) - Erythropoietic Protoporphyria
What are the side effects of Melanotan I?
Reported side effects include: Nausea (common), Skin darkening (intended effect), Headache, Fatigue, Injection site reactions. Individual responses vary based on dosage, duration, and personal health factors.
What is the typical dose of Melanotan I?
Community-reported common dose: 500-1000 mcg daily (loading), then 500-1000 mcg 1-2x weekly (maintenance) (Daily during loading (1-2 weeks), then 1-2x weekly maintenance). Range: 250-1000 mcg per injection. Administration: Subcutaneous implant (not injection). Community-reported doses. Not medical advice. Consult healthcare provider.
Related Peptides
Peptides commonly compared with Melanotan I or used in similar applications.
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Skin & HairMatrixyl
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Skin & HairMatrixyl 3000
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Skin & HairCopper Peptide AHK-Cu
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