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Research peptide

ARA-290

ARA-290 (cibinetide) is an 11-amino-acid peptide corresponding to the helix-B surface of erythropoietin.

By The Peptides Codex Editorial TeamIndividual review date not recorded

Page data last changed: . Chemistry registry snapshot: . Registry refreshes and identity assessments are separate from scientific content review.

Length
11 aa
Class
Research peptide
Function
Innate repair receptor agonist studied in tissue-protection models
Context
Investigational / clinical-stage research compound (not authorized by Health Canada)

EPO-derived peptide designed to keep tissue-protective signaling while avoiding red-blood-cell stimulation.

Also known as: cibinetide · cibinetide (INN)

Part of the Repair & recovery peptides cluster

Overview

ARA-290 (cibinetide) is an 11-amino-acid peptide corresponding to the helix-B surface of erythropoietin. It was engineered to engage the tissue-protective innate repair receptor without triggering erythropoiesis, and has been studied in clinical research on neuropathic and inflammatory conditions. It is not authorized by Health Canada for general use.

Source & context

Biological / chemical source: Synthetic peptide from the helix-B region of erythropoietin

Primary research or clinical context: Investigational / clinical-stage research compound (not authorized by Health Canada)

From erythropoietin to a repair peptide

Researchers isolated the part of the EPO molecule responsible for tissue protection rather than red-cell production and rebuilt it as a short synthetic peptide. ARA-290 selectively activates the innate repair receptor complex implicated in anti-inflammatory and cytoprotective signaling.

Clinical-research status

Under the name cibinetide, ARA-290 has been evaluated in clinical trials for conditions such as sarcoidosis-associated small-fiber neuropathy and holds orphan-drug interest in some jurisdictions. Approval status varies by country; this page is educational and not medical advice.

Sequence

One-letter sequence commonly cited for ARA-290 (educational; isoforms and modifications may differ):

XEQLERALNSS

XEQLERALNSS

X = non-canonical residue (X in the one letter sequence is pyroglutamate (pGlu).). X marks a non-canonical residue — see the structure block below. (Plotted as alanine on the wheel.)

ARA-29011 aa · C51H84N16O21 · ≈ 1,257.3 DaPEPTIDESCODEX.COMN-terminus →→ C-terminusX1E−2Q3L4E−5R+6A7L8N9S10S11nonpolarpolaracidicbasicGly / Pronon-canonical (X)Hydropathy (Kyte–Doolittle): ▮ hydrophobic (cyan) / ▮ hydrophilic (rose) · Side-chain charge at pH 7: + / −X = non-canonical residue (X in the one letter sequence is pyroglutamate (pGlu).)
ARA-290 — Structure cardDownload SVG
A1E2Q3L4E5R6A7L8N9S10S11
Helical wheel projection

Residues plotted ~100° apart around an α-helix — clustering of one color reveals an amphipathic face.

Analyze sequences in the playground →

Structure & chemistry

Molecular identity & reference confidence

Source-supported reference

Reference values are taken from the cited molecular record or curated profile. A database match is not independent laboratory verification; modifications, counter-ions, and formulations can change the measured mass.

Molecular form
ARA-290 (source record; form not independently established)
Species
Not established by this molecular identity audit
Termini (N / C)
Not specified / Not specified

Average reference mass

Reference policy updated: 2026-10-05

Molecular formula
C51H84N16O21
Average reference mass
≈ 1,257.3
Chemical modifications (IUPHAR record)

X in the one letter sequence is pyroglutamate (pGlu).

Identifiers

Chemistry values: IUPHAR/BPS Guide to Pharmacology, PubChem · fetched 2026-10-01.

Clinical development snapshot

ClinicalTrials.gov lists 4 registered studies with “ARA-290” as an intervention (snapshot 2026-09-06). A registry footprint is not evidence of efficacy or approval.

Registered studies
4
Highest phase reached
Phase 2
Active in latest 100
0
Most recent update
2024-10-04
Most recently updated studies
NCTTitlePhaseStatusUpdated
NCT06626971The Use of ARA290 for the Treatment of Diabetic Macular OedemaPhase 2terminated2024-10-04
NCT02039687Study of Efficacy of ARA 290 on Corneal Nerve Fiber Density and Neuropathic Symptoms of Subjects With SarcoidoPhase 2completed2017-04-18
NCT01933529ARA290 in T2D (Effects of ARA 290, an Erythropoietin Analogue) in Prediabetes and Type 2 Diabetes)Phase 2unknown2015-09-03
NCT02070783Cognitive and Neural Effects of ARA290Phase 2completed2014-02-25
See all on ClinicalTrials.gov →
Concentration math

ARA-290 — reconstitution calculator

Enter how much peptide is in the vial and how much diluent (e.g. bacteriostatic water) is added. The tool returns the resulting solution concentration — and, for any amount you type, the volume it corresponds to. This is educational arithmetic, not a dosing recommendation.

Reference form: ARA-290 (source record; form not independently established)Average reference mass: 1,257.3 Da

Syringe graduation
Solution concentration
5 mg/mL5,000 mcg/mL
mcg

Enter an amount to see the volume it corresponds to.

Educational concentration mathematics only. This tool does not recommend a dose, amount, or protocol, and nothing here is medical advice. Many peptides are not authorized by Health Canada for human use — see our reconstitution and bacteriostatic-water guides for context.

Open the ARA-290 calculator on its own page →

FAQ about ARA-290

What is ARA-290?+

ARA-290 (cibinetide) is an 11-amino-acid peptide corresponding to the helix-B surface of erythropoietin. It was engineered to engage the tissue-protective innate repair receptor without triggering erythropoiesis, and has been studied in clinical research on neuropathic and inflammatory conditions. It is not authorized by Health Canada for general use.

What Canadian product status is recorded for ARA-290?+

Canadian product status for ARA-290 has not been verified in this profile. No verified record here does not mean no authorization exists. Status depends on the product, formulation and use; consult Health Canada's product records.

What is the typical length of ARA-290?+

ARA-290 is commonly described as approximately 11 amino acids (Research peptide).

Related peptides

References & further reading

  1. 1.Shokrzadeh et al. (2020). An engineered non-erythropoietic erythropoietin-derived peptide, ARA290, attenuates doxorubicin induced genotoxicity and oxidative stress. Toxicol In Vitro
  2. 2.Bitto et al. (2018). Activation of the EPOR-β common receptor complex by cibinetide ameliorates impaired wound healing in mice with genetic diabetes. Biochim Biophys Acta Mol Basis Dis
  3. 3.Nairz et al. (2017). Cibinetide dampens innate immune cell functions thus ameliorating the course of experimental colitis. Sci Rep
  4. 4.Yao et al. (2021). Cibinetide Protects Isolated Human Islets in a Stressful Environment and Improves Engraftment in the Perspective of Intra Portal Islet Transplantation. Cell Transplant
  5. 5.Yao et al. (2020). Improvement of Islet Allograft Function Using Cibinetide, an Innate Repair Receptor Ligand. Transplantation
  6. 6.Lois et al. (2020). A Phase 2 Clinical Trial on the Use of Cibinetide for the Treatment of Diabetic Macular Edema. J Clin Med
  7. 7.Culver et al. (2017). Cibinetide Improves Corneal Nerve Fiber Abundance in Patients With Sarcoidosis-Associated Small Nerve Fiber Loss and Neuropathic Pain. Invest Ophthalmol Vis Sci
  8. 8.Awida et al. (2021). The Non-Erythropoietic EPO Analogue Cibinetide Inhibits Osteoclastogenesis In Vitro and Increases Bone Mineral Density in Mice. Int J Mol Sci
  9. 9.PubChem — compound summary for Cibinetide (CID 91810664)
  10. 10.Wikipedia — Cibinetide
Disclaimer: Educational content only. Not medical advice. Not instructions for human use. Research peptides and unapproved products may be restricted or illegal to market for human consumption in your jurisdiction. Consult qualified professionals and applicable law.
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