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Heart & Blood
Clinical

Rusfertide

Also known as: Mimrylo, PTG-300, TAK-121

A hepcidin-mimetic peptide that limits iron supply for red cell production. FDA-approved as Mimrylo (2026) for polycythemia vera. Prescription medication.

Last updated

Mechanism of Action

Rusfertide is a synthetic peptide that mimics hepcidin, the liver hormone that controls iron availability. It binds and degrades ferroportin, the iron exporter on gut cells and macrophages, which reduces iron delivery to the bone marrow. In polycythemia vera, restricting iron in this way slows excess red blood cell production and helps keep hematocrit controlled with fewer phlebotomies.

Half-life
Not well established
Administration Routes
Subcutaneous
Research Status
Clinical

Reported Benefits

  • Controls hematocrit in adults with polycythemia vera
  • Reduced the need for therapeutic phlebotomy (REVIVE, VERIFY)
  • Improves iron-deficiency markers caused by repeated phlebotomy

Potential Side Effects

  • Injection-site reactions (most common)
  • Anemia
  • Fatigue
  • New or worsening thrombocytosis (label warning)

Common Dosing

Mimrylo is given as a once-weekly subcutaneous injection, with the dose adjusted over time to keep hematocrit in the target range, and blood counts are checked regularly. Dosing is set and supervised by the prescribing clinician.

The dosing information above is aggregated from research literature and anecdotal community reports for educational purposes only. It is not a recommendation, prescription, or medical advice. Peptides are sold as research chemicals only and are not intended for human use.

Contraindications

  • No contraindications listed on the US label
  • Embryo-fetal toxicity: contraception advised (label warning)
  • Monitor for thrombocytosis with regular blood counts

No documented stacking partners for Rusfertide yet.

  • Rusfertide, a Hepcidin Mimetic, for Control of Erythrocytosis in Polycythemia Vera

    2024

    View
  • Pharmacokinetics, pharmacodynamics, and tolerability of an aqueous formulation of rusfertide (PTG-300), a hepcidin mimetic, in healthy volunteers: A double-blind first-in-human study

    2024

    View

Yes. The FDA approved rusfertide as Mimrylo on August 28, 2026 for erythrocytosis in adults with polycythemia vera. It was developed by Protagonist Therapeutics with Takeda, and approval rested mainly on the phase 3 VERIFY trial.

In VERIFY, most patients on rusfertide needed no phlebotomy during the assessment window, compared with about a third on placebo. It is used alongside a hematologist's overall plan for polycythemia vera, which may still include other therapies.

PeptideChat is for educational and research purposes only. Nothing on this site constitutes medical advice. Peptides are sold as research chemicals only and are not intended for human use. These statements have not been evaluated by the FDA and are not intended to diagnose, treat, cure, or prevent any disease. PeptideChat is an independent educational resource — not a pharmacy, compounding, or 503A/503B outsourcing facility — and does not sell products or provide medical advice.