Peptide Protocol

ARA-290: innate repair receptor agonist — nerve and tissue healing.

Non-hematopoietic EPO analog targeting the innate repair receptor. Neuroprotective, anti-inflammatory, and metabolic. SubQ.

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4–8 mg
Per Dose
4–12 weeks
Cycle
SubQ
Route
3× weekly
Frequency
Overview

What is ARA-290?

ARA-290 was engineered by the Gordijn/Brines group at Yale University to specifically target the innate repair receptor (EPOR/CD131 heterodimer) while avoiding the erythropoiesis-stimulating homodimeric EPOR. This selectivity allows activation of tissue-protective EPO signaling without erythrocytic effects — eliminating the thrombosis and polycythemia risks of therapeutic EPO.

Clinical trials have demonstrated ARA-290's efficacy in painful diabetic neuropathy and sarcoidosis-associated small-fiber neuropathy — with significant improvements in nerve fiber density, pain scores, and autonomic function. It also shows promise for metabolic effects including improved insulin sensitivity and reduced inflammatory markers.

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Innate Repair Receptor
Selectively activates the EPOR/CD131 heterodimer on non-hematopoietic cells — triggering tissue-protective JAK2/STAT5 and PI3K/AKT signaling.
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Nerve Fiber Regeneration
Clinical data shows increased intraepidermal nerve fiber density in diabetic neuropathy — direct evidence of peripheral nerve regeneration.
📉
Anti-Inflammatory
Reduces macrophage-mediated inflammation and inflammatory cytokine production in multiple tissue types through IRR-mediated pathways.
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Metabolic Improvement
Improves pancreatic beta-cell survival and insulin sensitivity through IRR activation in metabolic tissues — independent of erythropoietic effects.
Dosing Protocol

Dosing Schedule

Parameters documented in published preclinical and clinical research.

⚠️ Research use only. The following documents parameters from published preclinical and clinical research. Not medical advice. Not for human consumption. Consult a licensed healthcare professional before any use.
PhaseDoseFrequencyDurationNotes
Clinical4 mg3× weekly SubQ4–12 weeksDose and schedule from published sarcoidosis and neuropathy trials.
Working dose4–8 mg3× weekly8–12 weeksSubQ abdomen or thigh. Clinical trials used 4 mg 3× weekly most commonly.
Maintenance4 mg2× weeklyOngoingLower-frequency maintenance after initial treatment course.
Off cycle4–8 weeksCycle off and reassess nerve and pain outcomes.
Safety Profile

Safety & Side Effects

✓ Generally Well Tolerated
Phase 2 clinical trial data in diabetic and sarcoidosis neuropathy
No erythropoiesis — no thrombosis or polycythemia risk
Documented peripheral nerve fiber regeneration in humans
Excellent tolerability in published clinical trials
⚠ Potential Concerns
Not FDA-approved — research compound status
Limited long-term safety data beyond 12-week trials
Subcutaneous administration required — no oral formulation
Production and quality control variable in research suppliers
⚠️
Research use onlyThis page is an educational reference. None of this constitutes medical advice. Consult a qualified professional before any use. All compounds are for research purposes only.
Evidence Base

Academic References

  1. [1]
    Brines M, et al. (2008). Nonerythropoietic, tissue-protective peptides derived from the tertiary structure of erythropoietin. Proc Natl Acad Sci USA. 105(31):10925–30. PubMed ↗
  2. [2]
    Dahan A, et al. (2013). ARA 290, a synthetic erythropoietin mimetic, reduces pain in patients with fibromyalgia. Pain. 154(9):1526–33. PubMed ↗
  3. [3]
    Culver DA, et al. (2017). Pilot study of ARA 290, an erythropoietin analog, in sarcoidosis-associated small-fiber neuropathy. Sarcoidosis Vasc Diffuse Lung Dis. 34(2):103–13. PubMed ↗
  4. [4]
    Heij L, et al. (2015). ARA290 treatment improves symptoms in patients with sarcoidosis. Sarcoidosis Vasc Diffuse Lung Dis. 32(3):237–45. PubMed ↗
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