Anzupgo — delgocitinib
Named-patient access overview. Anzupgo is coordinated by Reserve Meds for international patients via physician-led cross-border sourcing.
About Anzupgo
Anzupgo (delgocitinib) is manufactured by LEO Pharma and indicated for Chronic hand eczema in adults. It is a approved by the US FDA in 2025 and may be accessible to international patients through Named Patient Program or personal-import pathways.
How Reserve Meds coordinates Anzupgo
- Patient or treating physician submits a named-patient request.
- Clinical team verifies appropriateness of Anzupgo for the patient and destination country.
- Treating physician issues prescription and clinical justification.
- Country-specific NPP / personal-import documentation is prepared.
- Anzupgo is sourced from a DSCSA-compliant US specialty wholesaler with full serial traceability.
- Shipment is coordinated to the patient's physician or hospital pharmacy (cold-chain where required).
Access by country
We have documented named-patient access pathways for Anzupgo in the countries below. Each page outlines the destination-country regulatory posture, typical timeline, and physician-credential requirements.
Anzupgo in BahrainNamed-patient access, timeline, and regulatory notes
Anzupgo in OmanNamed-patient access, timeline, and regulatory notes
Anzupgo in Saudi ArabiaNamed-patient access, timeline, and regulatory notes
Anzupgo in Sri LankaNamed-patient access, timeline, and regulatory notes
Start a request for Anzupgo
Submit a 60-second intake. Our clinical team responds within one business day with case-specific feasibility, timeline, and a formal quote.