Livdelzi — seladelpar
Named-patient access overview. Livdelzi is coordinated by Reserve Meds for international patients via physician-led cross-border sourcing.
About Livdelzi
Livdelzi (seladelpar) is manufactured by Gilead/CymaBay and indicated for Primary biliary cholangitis. It is a PPAR-delta approved by the US FDA in 2024 and may be accessible to international patients through Named Patient Program or personal-import pathways.
How Reserve Meds coordinates Livdelzi
- Patient or treating physician submits a named-patient request.
- Clinical team verifies appropriateness of Livdelzi for the patient and destination country.
- Treating physician issues prescription and clinical justification.
- Country-specific NPP / personal-import documentation is prepared.
- Livdelzi 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 Livdelzi in the countries below. Each page outlines the destination-country regulatory posture, typical timeline, and physician-credential requirements.
Livdelzi in BahrainNamed-patient access, timeline, and regulatory notes
Livdelzi in BangladeshNamed-patient access, timeline, and regulatory notes
Livdelzi in EgyptNamed-patient access, timeline, and regulatory notes
Livdelzi in KuwaitNamed-patient access, timeline, and regulatory notes
Livdelzi in OmanNamed-patient access, timeline, and regulatory notes
Start a request for Livdelzi
Submit a 60-second intake. Our clinical team responds within one business day with case-specific feasibility, timeline, and a formal quote.