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Forzinity, elamipretide

Named-patient access overview. Forzinity is coordinated by Reserve Meds for international patients via physician-led cross-border sourcing.

About Forzinity

Forzinity (elamipretide) is manufactured by Stealth BioTherapeutics and indicated for Barth syndrome, adults/children >=30 kg. It is an oral small molecule approved by the US FDA in 2025 and may be accessible to international patients through Named Patient Program or personal-import pathways.

How Reserve Meds coordinates Forzinity

  1. Patient or treating physician submits a named-patient request.
  2. Clinical team verifies appropriateness of Forzinity for the patient and destination country.
  3. Treating physician issues prescription and clinical justification.
  4. Country-specific NPP / personal-import documentation is prepared.
  5. Forzinity is sourced from a DSCSA-compliant US specialty wholesaler with full serial traceability.
  6. Shipment is coordinated to the patient's physician or hospital pharmacy (cold-chain where required).

Access by country

Reserve Meds publishes a detailed country deep-dive for Forzinity in every market we coordinate. Each page below covers the destination-country regulatory pathway (named-patient framework), real costs in local currency and USD, indicative timelines, physician-credential requirements, and cold-chain handling for the route into that country. Tap any country to read the full deep-dive.

Start a request for Forzinity

Submit a 60-second intake. Our clinical team will reach out as our first cohort opens with case-specific feasibility, timeline, and a formal quote.

Join the Forzinity waitlist