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Rare Medication

Medicine profile

Sotorasib

sotorasib

Sotorasib (Lumakras, Lumykras): An oral KRAS G12C inhibitor for previously treated non-small cell lung cancer carrying that mutation. Procurement-oriented reference for licensed buyers - not medical advice, and availability depends on region and authorization.

Not listedFDA drug shortage database - checked 24 Oct 2026Shortage page

What this medicine is commonly used for

Procurement teams reference Sotorasib when aligning formulary decisions, documenting a named patient request, or preparing a quotation for a destination country where the product is not routinely stocked.

Informational only. Treatment decisions belong to qualified clinicians and to local labeling.

Shortage and sourcing context

Requests usually follow molecular testing, so timelines matter: the patient is identified before a supply route exists in that country. Reimbursement status and authorization differ widely between markets, which is what most inquiries turn on.

How it is presented

Examples of presentations referenced for this medicine. Actual market presentations vary by country and registration, so check the pack in front of you.

  • Tablet

Who typically asks us about this medicine

  • Patients and families who cannot fill a prescription locally
  • Hospital pharmacies managing formulary access during a shortage
  • Clinics with defined treatment pathways and continuity of care
  • Procurement teams coordinating licensed cross-border sourcing
Full reference text(expand)

Sotorasib (Lumakras, Lumykras): An oral KRAS G12C inhibitor for previously treated non-small cell lung cancer carrying that mutation. Procurement-oriented reference for licensed buyers - not medical advice, and availability depends on region and authorization.

Procurement context

Procurement teams reference Sotorasib when aligning formulary decisions, documenting a named patient request, or preparing a quotation for a destination country where the product is not routinely stocked.

What makes it hard to source

Requests usually follow molecular testing, so timelines matter: the patient is identified before a supply route exists in that country. Reimbursement status and authorization differ widely between markets, which is what most inquiries turn on.