In a randomized, double-blind, placebo-controlled trial, afamelanotide increased pain-free light exposure and reduced phototoxic symptoms in patients with erythropoietic protoporphyria.
Melanotan I
Melanotan I (afamelanotide) is a synthetic analog of α-melanocyte stimulating hormone that selectively targets MC1 receptors to stimulate melanin production.
Overview
Last reviewed: 2026-08-18
Identity & Aliases
Also known as
Status: Research peptide - not approved for human consumption; FDA-approved SCENESSE® implant exists for rare conditions
Full composition (formula, molecular weight, sequence) in Quick Facts →
Research Areas
Available Evidence
Afamelanotide (the approved 'melanotan I' analog) is FDA-approved (2019) and EMA-approved for erythropoietic protoporphyria; a placebo-controlled trial (NEJM 2015) showed increased pain-free light exposure and improved quality of life in EPP patients.
Preclinical models demonstrate MC1R-mediated eumelanin synthesis and photoprotective effects.
In vitro studies show NDP-MSH activation of the melanocortin-1 receptor stimulates melanogenesis in melanocytes.
Use of unregulated 'melanotan' products for cosmetic tanning is not FDA-approved; safety (e.g., changes in nevi, melanoma risk) is not established, and dermatology organizations have warned against unregulated use.
Key Studies & Findings
FDA approved afamelanotide (Scenesse) to increase pain-free light exposure in adults with erythropoietic protoporphyria.
Benefits & Effects
Unlike the FDA-approved SCENESSE® implant, injectable form allows flexible dosing and can be administered at home
Produces visible tanning within 1-2 weeks with proper UV exposure
No side effects data available yet.
This peptide may have limited safety data.
Limitations & Open Questions
Pharmacology
Reported Research Dosing
Reported values from research literature and community protocols. Educational reference only — not a dosing recommendation or medical advice.
0.25mg
Research Protocols
Initial Tanning (Light Skin)
- Dose
- 0.25mg
- Frequency
- 2x daily
- Route
- Subcutaneous injection
Maintenance Tanning
- Dose
- 0.5mg
- Frequency
- 1x daily
- Route
- Subcutaneous injection
Enhanced Pigmentation
- Dose
- 0.5mg
- Frequency
- 2x daily
- Route
- Subcutaneous injection
Photoprotection Only
- Dose
- 0.25mg
- Frequency
- 1x daily
- Route
- Subcutaneous injection
Research protocols are for educational purposes only. Always consult qualified medical professionals.
Frequently Asked Questions
Is Melanotan I the same as the FDA-approved drug?
The approved drug Scenesse is afamelanotide, a pharmaceutical form of 'melanotan I' (NDP-MSH), approved only for erythropoietic protoporphyria — not for tanning.
Is melanotan safe for tanning?
Unregulated melanotan use for tanning is not approved; safety data are lacking and dermatology organizations have issued warnings.
Research Citations
Safety Profile Assessment (2006)
(2006)
MT-I Photoprotection Study (2004)
(2004)
Tanning Efficacy Comparison (2003)
(2003)
Related Resources
Quick Facts
Mechanism
Subcutaneous injection delivers Melanotan I directly into systemic circulation with 100% bioavailability. 30-minute half-life requires multiple daily injections for sustained MC1R activation and melanin production.
Safety Information
Research peptide - not approved for human consumption, sold for research purposes only. Start with lower doses to assess individual tolerance and response. Monitor moles and skin changes - perform regular self-examinations. Use proper sterile injection technique to prevent infections. Maintain UV protection despite enhanced tanning - still risk of overexposure.
Citations
31.Safety Profile Assessment (2006)
(2006)
2.MT-I Photoprotection Study (2004)
(2004)
3.Tanning Efficacy Comparison (2003)
(2003)