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Lunsumio in Jordan

How patients in Jordan access Lunsumio (CD20xCD3 bispecific) via Named Patient Program.

Lunsumio - overview

Lunsumio (CD20xCD3 bispecific) is manufactured by Roche / Genentech and indicated for relapsed or refractory follicular lymphoma in adults after two or more lines of systemic therapy. It is an intravenous bispecific T-cell engager with step-up dosing approved by the US FDA in 2022 and may be accessible to patients in Jordan through a Named Patient Program or personal-import pathway.

Access in Jordan

Jordan's JFDA operates a compassionate-use framework for unregistered drugs; requires physician and JFDA approval.

How Reserve Meds coordinates access in Jordan

  1. Patient or treating physician submits a request.
  2. We verify clinical appropriateness and Jordan-specific eligibility.
  3. Treating physician in Jordan issues prescription and clinical justification.
  4. Country-specific NPP/personal-import forms are prepared and filed.
  5. We source Lunsumio from a DSCSA-compliant US specialty wholesaler.
  6. Cold-chain shipment to the patient's physician or hospital pharmacy in Jordan.

Typical timeline for Jordan

End-to-end, most requests are completed in 2-6 weeks. Jordan's tier 2 regulatory maturity typically supports moderate processing times.

What patients and physicians in Jordan ask

  • Is the pathway legal in Jordan? Yes - it operates under Jordan's established NPP or personal-import framework.
  • Does my insurance cover it? Typically no for NPP drugs; patient prepayment is standard.
  • What physician credentials do I need? A licensed physician in Jordan able to issue the prescription and clinical justification.
  • What if the drug is in shortage? We will inform you upfront and decline rather than promise what we cannot deliver.
  • Can I re-supply? Yes - for chronic therapies we arrange ongoing re-supply.

Start a request for Lunsumio in Jordan

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AI Regulatory Review Agent, preliminary signal
Biologic drug requires JFDA import confirmation for the specific patient indication. Cold-chain shipping validated. Typically 2-4 week approval.
Rule: biologic_moh_confirmation • Reviewed 2026-04-22

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Review & oversight. Content on this page is reviewed by Reserve Meds's clinical and regulatory team. A US-licensed pharmacist reviews every prescription before dispensing. Regulatory posture is informational, not legal advice; case-specific questions route to retained outside counsel. Review methodology ›
Last medically reviewed: .