Earn points on every order · Free shipping on orders over $159 · New products in stock
← Back to Compound Library
Tissue Repair and Recovery

ARA-290 (Cibinetide)

A nerve-repair and anti-inflammatory peptide for neuropathy, burning, tingling, numb, or painful small nerves. Built from a piece of EPO (the red-blood-cell hormone), but deliberately stripped of the blood-building part; it repairs tissue without thickening your blood. One of the few peptides here with real human trial data.

Research referenceCommunity compiled
Research & reference information

This profile compiles research and community-sourced reference information for educational purposes. Information may evolve as research and community knowledge develop. It is not individualized medical advice.

Overview

A nerve-repair and anti-inflammatory peptide for neuropathy, burning, tingling, numb, or painful small nerves.

Built from a piece of EPO (the red-blood-cell hormone), but deliberately stripped of the blood-building part; it repairs tissue without thickening your blood.

One of the few peptides here with real human trial data.

What It Does

11-amino-acid peptide from the helix-B domain of erythropoietin. Selectively activates the Innate Repair Receptor (IRR), the EPOR/CD131 (β- common) heterodimer, not the classic EPO receptor.

Drives tissue protection, small-nerve-fiber regeneration, and resolution of inflammation, without stimulating erythropoiesis.

Reconstitution

Vial SizeBAC Water / SolventConcentration
10 mg+ 1.25 mL8 mg/mL
16 mg+ 2 mL8 mg/mL
Interactive tool

Reconstitution Calculator

Enter the vial amount and diluent volume to calculate concentration. If you already have a target amount, you can also convert it to liquid volume and syringe markings. This tool does not recommend a target amount.

Calculated concentration—Enter both values above.
Optional conversion

Enter a target amount you already have and select the syringe capacity.

Calculated draw—Enter concentration inputs and a target amount.

Mathematical reference only. The calculator does not determine an appropriate target amount. Syringe capacity only changes the maximum volume that fits.

Protocol

PhaseFrequencyAmountNotes
Week 1 (ramp)Daily SubQ2 mgCommon community start, assess tolerance before the full dose.
Weeks 2–4Daily SubQ4 mgThe trial dose. Phase 2 tested 1–8 mg/day; 4 mg was the therapeutic target and 8 mg gave no extra benefit, do not
OffAfter 28–Trials ran a single 28-day course. Reassess before repeating; no long-term dosing data exists. days
Cycle & Timing

a 28-day daily course (what the trials actually did), then reassess. Community practice repeats courses with a break rather than dosing continuously.

Timing

Daily SubQ, anytime; consistency matters more than time of day.

Evidence Context

Phase 2 human RCT data (sarcoidosis small-fiber neuropathy), unusually strong for this catalog, but single-institution and no Phase 3.

Population Considerations

Unisex, the IRR repair pathway is not sex-specific and trials enrolled both men and women at the same 4 mg dose; no cycle effect. Avoid in pregnancy (no data).

Handling & Stacking

Injection site
SubQ abdomen or thigh. Rotate. Bioavailability >85% SubQ.
Storage
  • Freeze-dried: -4°F.
  • Reconstituted: 36–46°F.
  • Best used within 28 days; protect from light.
  • There's no reliable community potency figure for ARA-290, a robust 11-aa peptide with no published data, so treat the vial as sterility-limited at ~28 days; a best-guess default, not a measured window.
Side effects
  • Well tolerated in trials.
  • Occasional mild injection-site reaction.
  • No rise in hemoglobin, hematocrit, reticulocytes, or blood pressure at 4 mg/day × 28 days; the key difference from EPO.
What to expect
  • Neuropathic pain and symptom scores improved over the 28-day course; structural nerve regrowth (corneal nerve fiber density) measurable by day 28.
  • Serum half-life is only minutes, the effect comes from receptor signalling, not blood levels, so don’t chase frequency.
  • Supply math at the 4 mg/day target: 16mg → 4 days/vial (7 vials per 28-day course) | 10mg → 2.5 days/vial (~11 vials).
  • At 2 mg/day, halve it.
Pairs well with
BPC-157 (broader tissue repair); KPV (additive anti-inflammatory); Alpha-lipoic acid / B12 (standard neuropathy support)
Avoid
Active malignancy (EPO-receptor biology, theoretical). Erythropoietin / ESA therapy (overlapping receptor pathway). Pregnancy, lactation.
Approved drug
  • Four drugs are FDA-approved for nerve pain: pregabalin (Lyrica), duloxetine (Cymbalta), tapentadol ER (Nucynta) and the 8% capsaicin patch (Qutenza).
  • Proven and prescribable, reasonable to try first.

Safety & Patient Education

Contraindications
Active malignancy, theoretical, via EPO-receptor pathway biology Concurrent erythropoietin / ESA therapy Pregnancy and lactation (no data)
Warnings
  • Not FDA-approved.
  • Holds orphan-drug designation for sarcoidosis-associated small-fiber neuropathy, but was never submitted for approval; development stalled after 2020 when the sponsor wound down All human data is Phase 2, single-institution (Netherlands), n ranging from under 40 to 64; no Phase 3 replication Longest human exposure studied is 28 days, long-term safety is unknown Interacts with EPO-receptor complexes and vascular endothelium, caution with pre-existing cardiovascular disease Vial quality varies, request a COA for each lot
Drug interactions
Erythropoietin / ESAs (epoetin, darbepoetin): overlapping receptor pathway; do not combine Immunosuppressants / biologics: ARA-290’s anti-inflammatory effect may confound response markers, coordinate monitoring, don’t replace prescribed therapy No known interaction with the other peptides in this guide
Labs
  • Compound-specific: CBC at baseline + end (confirm hematocrit/hemoglobin are unchanged, they should be).
  • CMP baseline.
  • Out of range?
  • A rising hematocrit is NOT expected on ARA-290, investigate another cause.
Stop criteria
Rising hematocrit or hemoglobin (unexpected, evaluate) New or worsening cardiovascular symptoms Persistent injection-site reaction beyond 7 days
Patient education
This treats nerve symptoms, not the underlying disease causing them; keep treating the root cause Give it the full 28 days; nerve regrowth is slow and the trial endpoints were measured at day 28 More is not better: 8 mg/day performed no better than 4 mg in trials Aseptic technique: swab the septum and site, single-use sterile needle every injection, never share vials Mark the date of first puncture; inspect for cloudiness or particulates before each use Sharps disposal in an FDA-cleared container
References
NCT02039687 (Phase 2b) · IOVS, corneal nerve fiber · PubMed · IRR mechanism · FSR webinar