Krazati in Egypt

How patients in Egypt access Krazati (adagrasib) via Named Patient Program.

Krazati - overview

Krazati (adagrasib) is manufactured by BMS / Mirati Therapeutics and indicated for KRAS G12C‑mutated cancers. It is a Small molecule approved by the US FDA in 2022 and may be accessible to patients in Egypt through a Named Patient Program or personal-import pathway.

Access in Egypt

Egypt's EDA permits personal-use import of non-registered drugs under physician supervision; process is paperwork-heavy but viable.

How Reserve Meds coordinates access in Egypt

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

Typical timeline for Egypt

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

What patients and physicians in Egypt ask

  • Is the pathway legal in Egypt? Yes - it operates under Egypt'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 Egypt 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.

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GREEN
AI Regulatory Review Agent — preliminary signal
Small-molecule specialty therapy with clear named patient pathway in Egypt via EDA. Oral delivery; standard logistics.
Rule: sm_specialty_clear_pathway • Reviewed 2026-04-22

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AI disclosure & medical review. Content on this page is reviewed by Reserve Meds's AI clinical and regulatory review agents. A US-licensed human pharmacist (dispensed by Altima Care, US-licensed specialty pharmacy) reviews every prescription before dispensing. Regulatory posture is AI-summarized and not legal advice; case-specific questions route to retained outside counsel. Last medically reviewed: .
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