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Delgocitinib bulk supplier for pharma manufacturers

Delgocitinib 2% Suppliers & Bulk Manufacturers

Available Forms: Creams

Available Strengths: 2%

Reference Brands: Anzupgo (USA/EU)

Category: Derma Drugs

Delgocitinib is a topical Janus kinase (JAK) inhibitor used to treat moderate-to-severe chronic hand eczema in adults. It works by blocking the JAK-STAT signaling pathway, which reduces inflammation and skin lesions. Applied as a 2% cream to affected areas, it helps control eczema symptoms when topical corticosteroids are insufficient or unsuitable. It is not a systemic drug or narcotic and is used only on the skin.

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Product Description:

Delgocitinib is a topical pan-JAK inhibitor, blocking all four Janus kinases — JAK1, JAK2, JAK3 and TYK2. Those enzymes transmit signals from a wide range of inflammatory cytokine receptors, so inhibiting them interrupts several of the pathways that drive eczema at once. Applied to skin, it acts locally with low systemic exposure, which is the point: oral JAK inhibitors carry class warnings for serious infection, thrombosis and malignancy, and a topical formulation is intended to avoid that.

It is used twice daily for moderate to severe chronic hand eczema in adults for whom topical corticosteroids are inadequate or unsuitable — a condition that is disabling, often occupational, and until recently had almost no dedicated treatment beyond steroids and oral alitretinoin. In trials it improved disease severity and itch substantially compared with vehicle cream. Local adverse effects are uncommon; application site reactions are mild.

Sourcing notes. Originator product, on patent, no generic. Approved in the European Union in 2024 and by the FDA in 2025, with a paediatric extension under review. Supply is through authorised distribution. Because the indication is narrow and newly defined, reimbursement status largely determines volume in each market.

How Delgocitinib is supplied today, and licensing ahead of patent expiry

Where delgocitinib is approved

Checked 3 Oct 2026
MarketStatusBrand · regulator · date
Japan Approved Corectim ointment · MHLW · Jan 2020
European Union Approved Anzupgo cream · European Commission · Sep 2024
United States Approved Anzupgo cream · FDA · Jul 2025
Generic / biosimilar None None approved as of the check date

Not approved in your country? A hospital or doctor can often still import it for a named patient, through a special-access, import-permit or compassionate-use route. We confirm which route applies in your country and the documents needed before quoting. Ask about named-patient supply →

Named-patient import Where a patient needs the product in a market where it is not registered, named-patient import is the lawful route. It requires the treating physician's documentation and authorisation from the destination regulator. We handle this pathway. Named-patient access
Authorised distribution For registered markets, supply runs through the manufacturer's authorised distribution channel. We can identify the authorised route for your market and tell you whether the product is registered there at all. Innovator sourcing
A genericised alternative Where the clinical requirement is the drug class rather than this specific molecule, there is often an off-patent alternative that is faster to register and materially cheaper. Tell us the indication and target market and we will say plainly whether one exists. Discuss alternatives
Licensing and generic development Patents expire country by country, and in many countries development and dossier filing can start before expiry under research and regulatory-review exemptions. We connect manufacturers developing this molecule, dossier holders, licensees and tech-transfer partners for markets where it is, or will become, off-patent. Partner on this molecule
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Frequently Asked Questions

Anzupgo (Delgocitinib) is developed and sold by LEO Pharma (Corectim in Japan, Japan Tobacco / Torii). PharmaTradz handles enquiries for authorised supply of the originator product, named-patient import where it is not registered, and licensing or development work ahead of patent expiry.

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