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Breyanzi in Pakistan

How patients in Pakistan access Breyanzi (lisocabtagene maraleucel) via Named Patient Program.

Breyanzi - overview

Breyanzi (lisocabtagene maraleucel) is manufactured by BMS and indicated for DLBCL, CLL/SLL, FL, MCL. It is a CAR-T (CD19) approved by the US FDA in 2021 and may be accessible to patients in Pakistan through a Named Patient Program or personal-import pathway.

Access in Pakistan

Pakistan's DRAP permits personal-use import of unregistered specialty drugs; documentation-heavy process.

How Reserve Meds coordinates access in Pakistan

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

Typical timeline for Pakistan

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

What patients and physicians in Pakistan ask

  • Is the pathway legal in Pakistan? Yes - it operates under Pakistan'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 Pakistan 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 Breyanzi in Pakistan

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YELLOW
AI Regulatory Review Agent, preliminary signal
Cell/gene therapy to Pakistan is technically permissible via personal import but requires specialty cold-chain, autologous collection coordination, and case-by-case regulatory confirmation. Expect 6-12 week lead time.
Rule: gene_therapy_specialty_logistics • 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: .