ARA-290
Summary
ARA-290 (cibinetide) is an erythropoietin-derived peptide studied for tissue protection, nerve repair and inflammation. It signals through the innate repair receptor and, unlike EPO, does not stimulate red-blood-cell production. It remains an investigational research compound.
Quick facts
| Also known as | Cibinetide, Helix B Surface Peptide (HBSP), pyroglutamate HBSP (pHBSP), ARA 290 |
| Category | Tissue-protective / anti-inflammatory peptide |
| Status | Investigational — not FDA-approved |
| CAS | 1208243-50-8 |
| Formula | C51H84N16O21 |
| Molecular weight | 1257.3 g/mol |
| Sequence | pGlu-Glu-Gln-Leu-Glu-Arg-Ala-Leu-Asn-Ser-Ser (11 aa; N-terminal pyroglutamate) |
| Half-life | Very short plasma half-life (minutes); downstream biological effect outlasts plasma exposure |
| Storage | Lyophilized: store frozen, protect from light; reconstituted: refrigerate and use short-term |
In Plain English
ARA-290 is a lab-made peptide based on a piece of the natural hormone EPO — specifically the part that does not raise red blood cells. It is studied for calming inflammation and easing nerve pain and tissue damage. It is an experimental research compound.
ARA-290 (cibinetide) is an 11–amino-acid peptide engineered from erythropoietin (EPO) to keep EPO’s tissue-protective, anti-inflammatory activity while removing its blood-cell–stimulating effect. Developed by Araim Pharmaceuticals from the work of Anthony Cerami, ARA-290 reproduces a single surface of the EPO molecule and signals through a separate receptor — which is why researchers have studied it for nerve repair and inflammation without the clot-related risks that come with raising red-cell mass.
What is ARA-290?
ARA-290, also known as cibinetide, Helix B Surface Peptide (HBSP) or pyroglutamate HBSP (pHBSP), is a short linear peptide of eleven amino acids. Its sequence corresponds to the aqueous-facing surface of helix B of erythropoietin — the part of the EPO molecule that does not contact the classic erythropoietic receptor. Because it copies only this “tissue-protective” face, ARA-290 retains EPO’s repair signalling but is non-erythropoietic: it does not meaningfully raise red blood cell counts. The N-terminal residue is a cyclised glutamine (pyroglutamate), which is reflected in the pHBSP name. It is classed as a tissue-protective, anti-inflammatory research peptide.
How ARA-290 is studied to work
The central idea behind ARA-290 is receptor selectivity. Erythropoietin can act on two different receptor assemblies, and ARA-290 was designed to engage only one of them.
- It binds the innate repair receptor (IRR) — a heterocomplex of the EPO receptor (EPOR) and the beta-common receptor (CD131).
- This receptor is expressed mainly on injured or inflamed tissue, not on red-cell precursors.
- It does not activate the homodimeric (EPOR)₂ receptor that drives erythropoiesis — hence no rise in hematocrit.
- Downstream signalling reported in the literature includes JAK2/STAT3 and PI3K/Akt, plus anti-apoptotic Bcl-2–family pathways.
- The net studied effects are anti-inflammatory, anti-apoptotic, reduced vascular permeability and pro-repair.

Reported effects and benefits in the research literature
Across preclinical and early clinical work, ARA-290 has been studied mainly as a tissue-protective and nerve-repair agent. Reported areas of interest include:
- Neuropathic pain and small-fibre neuropathy — the most-studied application.
- Sarcoidosis-associated small-fibre neuropathy — reduced pain alongside objective signs of nerve-fibre regeneration.
- Type 2 diabetic neuropathy — improved neuropathic symptom scores and some metabolic measures.
- Diabetic macular edema — listed as an investigational indication on an anti-permeability rationale.
- Wound healing and general anti-inflammatory tissue protection — largely preclinical and mechanistic.
What this does not mean: these are early-phase findings in specific patient groups, often with small numbers. None of them establish ARA-290 as a proven treatment, and nothing here is guidance for personal use. Reported regulatory designations are investigational status, not marketing approval.

What the human evidence shows
Human data for ARA-290 come from small, early-phase trials. A 2012 randomized pilot in sarcoidosis patients with small-fibre neuropathy (Heij and colleagues, Molecular Medicine, n = 22) found intravenous ARA-290 was well tolerated and improved neuropathic-symptom scores. A larger Phase 2b study (NCT02039687) used corneal confocal microscopy as an objective endpoint and reported a significant increase in corneal nerve-fibre abundance (on the order of 23% at the 4 mg dose), more regenerating intra-epidermal nerve fibres, and clinically meaningful pain reduction in patients with moderate-to-severe pain. A separate Phase 2 trial in type 2 diabetes (Brines and colleagues, 2015) reported improved PainDetect neuropathic-symptom scores plus modest improvements in HbA1c and lipid profile.
Despite these encouraging signals, ARA-290 / cibinetide is not approved by the FDA or any major regulator for any indication. It remains investigational. Orphan-drug and fast-track designations have been reported in company communications, but a designation is an early regulatory step, not evidence of efficacy or an approval.
Handling, storage and reconstitution (research context)
ARA-290 is supplied as a lyophilized (freeze-dried) powder for laboratory use. General peptide-handling principles apply:
- Lyophilized powder: kept frozen and protected from light and moisture for long-term storage.
- Reconstituted solution: refrigerated and used over a short period; minimize freeze–thaw cycles.
- Reconstitution with bacteriostatic water sets the concentration (mg/mL) — use the reconstitution calculator to work out concentration and draw volume, and see why syringe “units” are not a dose for the measurement math.
Cautions and considerations
- ARA-290 is a research compound, not an approved medicine.
- Its regulatory status is investigational; reported designations are not approvals.
- Purity and identity matter — a certificate of analysis (COA) documents what is actually in a vial.
- This page is informational only and not medical advice; it is intended for an audience of 21+.
Frequently asked questions
Is ARA-290 the same as EPO?
No. ARA-290 copies only one tissue-protective surface of the erythropoietin molecule. It shares EPO’s repair signalling but not its ability to stimulate red blood cell production.
Does ARA-290 raise red blood cell counts?
In the published research it is described as non-erythropoietic, because it does not activate the homodimeric EPO receptor that drives erythropoiesis. This is the main reason it was developed.
Is ARA-290 FDA-approved?
No. ARA-290 / cibinetide is investigational and has not been approved for any indication. Any reported orphan-drug or fast-track status is an early regulatory step, not an approval.
What is the innate repair receptor?
It is a receptor assembly combining the EPO receptor with the beta-common receptor (CD131). It appears on stressed or injured tissue and is the target through which ARA-290 is thought to act.
Related compounds and further reading
- BPC-157 — another widely discussed tissue-repair research peptide.
- TB-500 (Thymosin β4) — studied in healing and recovery contexts.
- GHK-Cu — a copper peptide studied for skin and tissue repair.
- How to reconstitute peptides and sterile technique — core handling guides.
- Browse the full peptide library and all guides.
Share this article
References
- PubChem: Cibinetide (CID 91810664)
- DrugBank: Cibinetide (DB13006)
- Heij et al. 2012, Molecular Medicine — ARA 290 in sarcoidosis small-fibre neuropathy
- Brines et al. 2015, Molecular Medicine — ARA 290 in type 2 diabetes
- Swartjes et al. — ARA 290, neuropathic pain and spinal microglia
- ClinicalTrials.gov — Cibinetide in sarcoidosis small-fibre neuropathy (NCT02039687)
For informational use only. Not medical advice; consult a qualified healthcare professional. 21+.
ARA-290 reconstitution calculator
Use the calculator below to find the concentration (mg/mL), draw volume and U-100 syringe units for ARA-290 once it is reconstituted with bacteriostatic water. ARA-290 has molecular formula C51H84N16O21 and a molecular weight of 1257.3 g/mol. Enter your vial amount and the water volume to see the lab math — informational use only, not dosing advice.
