Tecelra — afamitresgene autoleucel
Named-patient access overview. Tecelra is coordinated by Reserve Meds for international patients via physician-led cross-border sourcing.
About Tecelra
Tecelra (afamitresgene autoleucel) is manufactured by Adaptimmune and indicated for Synovial sarcoma. It is a TCR-T (MAGE-A4) 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 Tecelra
- Patient or treating physician submits a named-patient request.
- Clinical team verifies appropriateness of Tecelra for the patient and destination country.
- Treating physician issues prescription and clinical justification.
- Country-specific NPP / personal-import documentation is prepared.
- Tecelra 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 Tecelra in the countries below. Each page outlines the destination-country regulatory posture, typical timeline, and physician-credential requirements.
Tecelra in BangladeshNamed-patient access, timeline, and regulatory notes
Tecelra in EgyptNamed-patient access, timeline, and regulatory notes
Tecelra in NepalNamed-patient access, timeline, and regulatory notes
Tecelra in OmanNamed-patient access, timeline, and regulatory notes
Tecelra in QatarNamed-patient access, timeline, and regulatory notes
Tecelra in TurkeyNamed-patient access, timeline, and regulatory notes
Start a request for Tecelra
Submit a 60-second intake. Our clinical team responds within one business day with case-specific feasibility, timeline, and a formal quote.