Pharmacokinetic study, 1997
A phase 1 study in three subjects reported complete subcutaneous bioavailability with significant tanning effects lasting three weeks after treatment ended. Reported in the cited paper.
SourceResearch Use Only. Products listed are not for human or animal consumption. Statements have not been evaluated by the FDA.View full disclaimers →
Melanotan I, known as afamelanotide, is a selective MC1R agonist. As Scenesse it is approved for increasing light tolerance in adults with erythropoietic protoporphyria, a rare photosensitivity disorder, and is given as a subcutaneous implant by a clinician.
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Overview
Melanotan I, known as afamelanotide, is a selective MC1R agonist. As Scenesse it is approved for increasing light tolerance in adults with erythropoietic protoporphyria, a rare photosensitivity disorder, and is given as a subcutaneous implant by a clinician.
What the research reports
Outcomes described across the published Melanotan-I literature and ongoing study. Read each as research context, not a promised result.
Selective MC1R agonist use
Targets the MC1R receptor for melanogenesis without the sexual and appetite effects associated with the less selective Melanotan II. Reported in research settings.
Approved photoprotection use
Scenesse is approved to increase light tolerance in adults with erythropoietic protoporphyria, a rare genetic disorder causing severe phototoxic reactions to daylight.
Eumelanin increase findings
A phase 1 case series reported a 49 to 98 percent increase in skin eumelanin content after dosing over a two week period. Reported in research settings.
Complete bioavailability data
A 1997 pharmacokinetic study reported complete subcutaneous bioavailability with tanning effects persisting three weeks after treatment. Reported in research settings.
Clinician administered format
The approved implant is placed above the hip every 60 days by a healthcare provider, which builds in medical oversight. Reported in research settings.
Dosage and protocol
The clinical implant delivers 16 mg every 60 days. Research injection protocols report 0.25 to 1 mg daily across 14 to 28 days. Figures describe study protocols, not a personal regimen.
Clinical evidence
The published record for Melanotan-I, labeled by strength so you can see what is settled and what is emerging.
A phase 1 study in three subjects reported complete subcutaneous bioavailability with significant tanning effects lasting three weeks after treatment ended. Reported in the cited paper.
SourceA phase 1 case series in seven subjects reported a 49 to 98 percent increase in skin eumelanin content over a two week dosing period. Reported in the cited paper.
SourceA 2017 review linked unregulated melanotan use to melanocytic changes, dysplastic naevi and reported melanoma cases, a warning about black market supply. Reported in the cited paper.
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