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Afamelanotide bulk supplier for pharma manufacturers

Afamelanotide 16 mg Suppliers & Bulk Manufacturers

Available Forms: Subcutaneous implant

Available Strengths: 16 mg

Reference Brands: Scenesse (USA)

Category: Derma Drugs

Afamelanotide is a Derma Drugs product available as Subcutaneous implant in strengths 16 mg. It corresponds to the reference brand Scenesse (USA). Verified GMP manufacturers and suppliers on PharmaTradz offer it in bulk for import worldwide, with regulatory documentation and dossier support available on request.

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📘 Sourcing Guide

Product Description:

Afamelanotide is a synthetic peptide medication used to prevent phototoxic reactions and reduce pain caused by light exposure in patients with erythropoietic protoporphyria (EPP), a rare genetic photosensitivity disorder. It is marketed under the brand name Scenesse and is administered as a prolonged-release subcutaneous implant.

Afamelanotide acts as an agonist of the melanocortin-1 (MC1) receptor and is an analogue of the naturally occurring alpha-melanocyte-stimulating hormone (α-MSH). By mimicking the biological activity of α-MSH, afamelanotide stimulates melanocytes in the skin to increase the production and release of melanin. Elevated melanin levels enhance the skin’s tolerance to visible and ultraviolet light exposure.

The increased melanin provides photoprotective effects by reducing ultraviolet radiation-induced cellular DNA damage, limiting oxidative stress on membrane proteins, and helping maintain normal intracellular signaling processes in epidermal cells. Under physiological conditions, α-MSH is released by skin cells in response to ultraviolet radiation; afamelanotide replicates this protective mechanism in patients with impaired photoprotection.

Afamelanotide offers an effective preventive treatment option for managing light-induced pain and improving quality of life in individuals affected by erythropoietic protoporphyria.

Afamelanotide — third party manufacturing & bulk supply

Afamelanotide 16 mg is available through PharmaTradz for wholesale and bulk supply as well as on a third party (contract) manufacturing basis. Buyers sourcing this product generally take one of three routes:

Wholesale / bulk supply Stock or scheduled supply from an existing manufacturer. The fastest route where the product is already registered in your market.
Third party manufacturing Manufactured to your specification and packed under your own brand and label — suits distributors and brand owners building a portfolio in their market.
Dossier licensing Where a CTD, EU-CTD or ACTD dossier exists it can often be licensed for filing in your name, compressing market entry from years to months.

What to include when you enquire

  • Destination market — determines which manufacturers hold the right site-level approvals
  • First order quantity and estimated annual volume
  • Whether you need a registration dossier or the product is already registered
  • Packaging, labelling and language requirements
  • Incoterms and required shelf life

Manufacturers of Afamelanotide listed on PharmaTradz hold site-level approvals across WHO-GMP, EU-GMP, USFDA, ANVISA and TGA, verified at onboarding. Narcotic drugs and controlled substances are supplied strictly against valid import and export permits issued by the competent authorities.

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Frequently Asked Questions

Afamelanotide is used to prevent and reduce phototoxic reactions in adult patients with erythropoietic protoporphyria (EPP), a rare genetic disorder causing severe pain and skin damage upon exposure to sunlight.

Afamelanotide is made from the active pharmaceutical ingredient afamelanotide acetate, a chemically synthesized peptide analogue of alpha-melanocyte-stimulating hormone.

The trade name of afamelanotide is Scenesse.

Afamelanotide is developed and marketed by Clinuvel Pharmaceuticals.

The complete generic name is afamelanotide acetate.

The brand name is Scenesse.

Afamelanotide is manufactured at Clinuvel Pharmaceuticals’ approved manufacturing facilities in Europe and other regulated regions, depending on market authorization.

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