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Evidence: BAnti-InflammatoryNeuroprotection

ARA-290: Benefits, Dosage & FDA Status

ARA-290 (Cibinetide)

An 11-amino-acid peptide derived from the helix-B region of erythropoietin. Activates the tissue-protective receptor without erythropoietic side effects. Investigated for neuropathy and inflammation.

FDA Status

Not FDA-approved — Phase 2/3 trials for sarcoidosis-associated small fiber neuropathy

Typical Dose

Trial range: 1–4 mg subcutaneous daily

Evidence Grade

BLimited clinical + robust preclinical evidence

Half-Life

Minutes (effects last hours)

Routes of Administration

subcutaneous

First Synthesized

2010

Clinics Indexed

9 providers have offered ARA-290 in our tracked directory.

Mechanism of Action

Selective agonist at the EPOR/βCR heteromer (tissue-protective receptor) without binding the erythropoietic homodimer.

Key Reported Benefits

Benefits listed reflect commonly reported effects from clinical trials and practitioner use. Individual response varies. Evidence-grade B indicates limited clinical + robust preclinical evidence.

Reported Side Effects

  • Generally well-tolerated
  • Injection-site reactions

Contraindications

  • Pregnancy

Regulatory & Safety Context

FDA status: Not FDA-approved — Phase 2/3 trials for sarcoidosis-associated small fiber neuropathy

This page is for educational purposes only and does not constitute medical advice. Peptide use outside of an FDA-approved indication should be discussed with a licensed medical professional. Source quality, cold-chain storage, and injection hygiene all materially affect safety outcomes.

See state-by-state legality: US peptide legality by state →

References

Selected primary literature on ARA-290. Full PubMed records linked. Additional citations are available on request.

  1. PubMed PMID 27400146

Last reviewed: 2026-04-30

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