Peptide library › Skin & cosmetic
Afamelanotide
Also known as Scenesse
Melanocortin-1 receptor agonist implant approved to protect people with a rare light sensitivity disorder.
What people use it for
- Erythropoietic protoporphyria (EPP), to increase pain-free time in light (approved use)
- Vitiligo (research)
What Afamelanotide does in the body
A long-lasting version of alpha-MSH, the hormone that stimulates skin pigment. It activates the MC1R receptor on pigment cells, increasing eumelanin, which helps protect the skin from light.
Strength of evidence
Moderate: randomised trials in EPP showed more pain-free time in sunlight.
Look up the evidence
- Reviews on PubMed: Summaries of the published research
- Clinical trials on PubMed: Published studies in people
- ClinicalTrials.gov: Registered trials, past and ongoing
- Prescribing information (DailyMed, US): Official US label
- Patient leaflets (emc, UK): Official UK product information
Live searches of official databases. New to the terms? See the glossary.
Reported side effects & risks
- Nausea, headache
- Implant-site reactions
- Darkening of skin and moles; skin checks are advised
Who should avoid it or take extra care
- Pregnant or breastfeeding (contraception advised during treatment)
- History of melanoma or skin cancer
- Severe liver or kidney problems
Not a complete list. Check with a doctor or pharmacist about your own health and medicines.
Regulatory status
Approved as Scenesse in the EU (2014) and the US (2019) for adults with EPP, given by trained clinicians.
How it's taken
Route: Dissolving implant placed under the skin by a clinician, about every 2 months
How long it lasts (half-life): Released slowly from the implant over weeks
Keep track of Afamelanotide privately
Fiala is a free app for logging doses, tracking vials and setting reminders. No account, and everything you log stays on your phone.
Open Afamelanotide in Fiala How to install