Registered implant trials
- Reported quantity
- 16 mg controlled-release subcutaneous implant
- Frequency
- Every 2 months
- Study duration
- Up to 180 days per trial period, repeated seasonally
Pain-free sunlight exposure time was the primary endpoint.

Protocols · Cosmetic
Melanotan I as afamelanotide completed a full registered development programme for erythropoietic protoporphyria and is an approved medicine in the EU and US. It is the only compound in this cosmetic group with a proper regulatory dossier.
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Every figure on this page is a range reported in published literature or in a publicly documented study protocol. It is a record of what researchers used, not a recommendation, a therapeutic protocol, or advice. Peptide Intel Hub is an independent publication, sells nothing, and describes these compounds as in-vitro research reagents only.
Each row below describes one body of work. The model and population are part of the figure — a rodent per-kilogram quantity and a human trial quantity are not comparable.
Pain-free sunlight exposure time was the primary endpoint.
These earlier figures predate the implant formulation that became the registered product.
The same arithmetic for every vial size Melanotan I is supplied in, using a fixed 3 ml of bacteriostatic water. One unit on a U-100 insulin syringe is 0.01 ml, so the unit column below is simply the volume that carries the reported amount. Educational arithmetic only — not instructions, and not medical advice.
Melanotan I · 3 ml bacteriostatic water
| Vial size | Concentration | Per 1 unit |
|---|---|---|
| 10 mg | 3.33 mg/ml | 33 mcg |
No single reported amount applies to this compound, so only the concentration and the value of one unit are shown. Only the vial sizes this compound is actually supplied in are shown, and every figure assumes exactly 3 ml of bacteriostatic water. For any other volume, use the reconstitution calculator.
Research powder is typically 10 mg per vial; in 2 mL that gives 5 mg/mL. The registered product is an implant and cannot be replicated from powder.
Open the reconstitution calculatorThese are the published records the figures on this page are drawn from. Each one describes what researchers administered, in which model or population, and over what period. Quantities reported in a study are specific to that study's design and are not transferable guidance.
Langendonk JG, Balwani M, Anderson KE, et al. · N Engl J Med · 2015 · DOI 10.1056/NEJMoa1411481
Patients with erythropoietic protoporphyria received subcutaneous implants of afamelanotide (16 mg, an analog of alpha-MSH known as Melanotan-I) every 60 days for up to 6 months.
View the recordFabrikant J, Touloei K, Brown SM. · N Engl J Med · 2009 · DOI 10.1056/NEJMc0805682
Correspondence describing subcutaneous administration of an alpha-MSH analogue (afamelanotide/Melanotan-I) implant to protoporphyria patients.
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Peptide Intel Hub is an independent educational publication. We are not affiliated with, owned by, or the same company as Regena Peptides and Regena.app (regena-peptides.com / regena.app). We do not sell, supply, ship or take payment for any compound. Because readers regularly ask where compounds discussed in published studies can be sourced for laboratory work, we list Regena Peptides and Regena.app as suppliers we have verified and trust — every batch is released with a lot-matched third-party certificate of analysis (HPLC purity and mass-spectrometry identity). Outbound links are marked nofollow/sponsored and are provided to help readers, not to sell.