Vyloy — zolbetuximab
Named-patient access overview. Vyloy is coordinated by Reserve Meds for international patients via physician-led cross-border sourcing.
About Vyloy
Vyloy (zolbetuximab) is manufactured by Astellas and indicated for CLDN18.2+ gastric/GEJ. It is a CLDN18.2 mAb 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 Vyloy
- Patient or treating physician submits a named-patient request.
- Clinical team verifies appropriateness of Vyloy for the patient and destination country.
- Treating physician issues prescription and clinical justification.
- Country-specific NPP / personal-import documentation is prepared.
- Vyloy 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 Vyloy in the countries below. Each page outlines the destination-country regulatory posture, typical timeline, and physician-credential requirements.
Vyloy in BahrainNamed-patient access, timeline, and regulatory notes
Vyloy in EgyptNamed-patient access, timeline, and regulatory notes
Vyloy in KuwaitNamed-patient access, timeline, and regulatory notes
Vyloy in LebanonNamed-patient access, timeline, and regulatory notes
Vyloy in QatarNamed-patient access, timeline, and regulatory notes
Start a request for Vyloy
Submit a 60-second intake. Our clinical team responds within one business day with case-specific feasibility, timeline, and a formal quote.