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ARA-290 (Cibinetide)

Emerging
aka Cibinetide · ARA290 · pyroglutamate helix-B surface peptide
Healing Not FDA-approved for human use — investigational, sold for research only.

Educational information only — not medical advice. Many listed compounds are not FDA-approved for human use. Consult a licensed clinician before starting, changing, or stopping any protocol.

Overview

ARA-290, also known as cibinetide, is a synthetic peptide of 11 amino acids modeled on the tissue-protective domain of erythropoietin (EPO). It was engineered to keep EPO’s repair-promoting and anti-inflammatory signaling while removing its effect on red blood cell production.

It is most often discussed in the context of nerve health, where it has been studied for small-fiber neuropathy — including neuropathy associated with sarcoidosis — and for neuropathic symptoms in people with type 2 diabetes.

ARA-290 has been evaluated in early-phase human trials but is not approved by any major regulator for therapeutic use. It remains an investigational compound, and the evidence base is still limited.

How it works

ARA-290 selectively activates what researchers call the innate repair receptor (IRR), a receptor complex thought to combine the EPO receptor with the CD131 subunit. Native EPO also signals through this pathway, but ARA-290 was designed to engage tissue-protective signaling without triggering the erythropoietic effects that raise hematocrit.

Through this pathway, ARA-290 is reported in preclinical and early clinical work to reduce inflammation, protect cells from stress, and support regeneration of small nerve fibers. The precise mechanism in humans is not fully established.

Reported benefits

  • Improvement in small-fiber neuropathy symptom scores (early clinical data)
  • Increased corneal nerve fiber density, suggesting nerve-fiber regeneration (studied)
  • Reduced neuropathic symptoms in type 2 diabetes (early clinical data)
  • Anti-inflammatory and tissue-protective effects without raising red blood cell count

These are reported or studied effects from limited early-phase research, not guaranteed outcomes.

Considerations & side effects

Human data comes from small, early-phase trials, so the long-term safety profile of ARA-290 is not well characterized. In the studies conducted to date, it was generally well tolerated, with no significant changes in blood counts and mild reactions such as injection-site irritation among the effects reported.

Because ARA-290 is not an approved medicine, purity and quality vary in the research-chemical market. It is not a substitute for evaluation and treatment of neuropathy or any other condition by a qualified clinician.

Frequently asked

What is ARA-290?

ARA-290, also called cibinetide, is a synthetic 11-amino-acid peptide modeled on the tissue-protective region of erythropoietin (EPO). It has been studied mainly for small-fiber and diabetic neuropathy.

Is ARA-290 FDA-approved?

No. ARA-290 is an investigational compound that has been through early-phase clinical trials but is not approved by the FDA or any major regulator for therapeutic use. It is sold for research purposes only.

Does ARA-290 raise red blood cell count like EPO?

It was specifically designed not to. Published phase 2 trials reported no meaningful change in hemoglobin, hematocrit, or reticulocyte count, because ARA-290 targets the innate repair receptor rather than the erythropoietic pathway.

What has ARA-290 been studied for?

Mainly small-fiber neuropathy associated with sarcoidosis and neuropathic symptoms in type 2 diabetes, where early trials looked at nerve-fiber regeneration, symptom scores, and inflammation.

References

  1. Heij L, et al. Safety and efficacy of ARA 290 in sarcoidosis patients with symptoms of small fiber neuropathy: a randomized, double-blind pilot study.
  2. Dahan A, et al. ARA 290 improves symptoms in patients with sarcoidosis-associated small nerve fiber loss and increases corneal nerve fiber density.
  3. Brines M, et al. ARA 290, a nonerythropoietic peptide engineered from erythropoietin, improves metabolic control and neuropathic symptoms in patients with type 2 diabetes.

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