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A2R

Ara 290

Tissue-Protective Peptide | Innate Repair Receptor Agonist

Emerging Research
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What is Ara 290?

Ara 290 (also called Cibinetide) is a lab-made peptide modeled on part of the natural hormone erythropoietin, but engineered to activate a different receptor pathway so it doesn't stimulate red blood cell production the way erythropoietin does. Researchers have studied it in multiple Phase 2 clinical trials for tissue-protective and nerve-related research, and it holds FDA Orphan Drug status for several indications. Research-grade Ara 290 sold here is intended for laboratory research use only, not human or animal use.

Key terms:

Ara 290 is a synthetic heptapeptide.

Ara 290 (Cibinetide) is a lab-made peptide of 11 amino acids, modeled on erythropoietin (the hormone that tells the body to make red blood cells). It switches on a different target, the Innate Repair Receptor (IRR), which is linked to tissue protection. It does not raise red blood cell production. It has finished several Phase 2 clinical trials and holds FDA Orphan Drug status for several conditions.

Key research areas

  • Tissue-protective effects reported in clinical trials
  • Nerve regeneration effects reported in Phase 2 trials
  • Anti-inflammatory effects
  • Favorable safety profile reported in clinical trials
  • No hematopoietic effects or risk of polycythemia

Researched dosing

This table shows how researchers structure clinical study designs with Ara 290 — the dose ranges and schedules used in published trials, presented as research methodology, not usage instructions.

PhaseDoseFrequencyRoute
Neuropathy models4 mg dailyOnce dailySubcutaneous
Tissue-protection models1-8 mg dailyOnce dailySubcutaneous
Acute-phase protocols2 mg3x weeklyIntravenous
Standard study protocol4 mg dailyOnce daily for 28 daysSubcutaneous

Commonly cycled 4 weeks on, 0+ weeks off.

How it works

At the cell level, Ara 290 research looks at how the peptide activates a tissue-protective receptor pathway related to erythropoietin's receptor, without triggering red-blood-cell production — the terms below just name that signaling route.

Activates Innate Repair Receptor (IRR) through EPOR/β-common receptor complex, triggering tissue-protective signaling without erythropoietic effects

Pharmacokinetics

This chart shows how quickly a research dose of Ara 290 is absorbed and cleared in the study literature — read it like a timer: the peak is when levels are highest, then the curve trails off as the compound clears.

Peak
0.333 hr
Half-life
0.333 hrs
Cleared
~0 hrs

Based on pharmacokinetic studies

Research applications

This section lists the body systems and research areas scientists have studied for Ara 290 — largely nerve and tissue-protection research from Phase 2 trials — summarizing what's been studied in the literature, not medical claims about people.

Neuroprotection

Most studied

23% increase in corneal nerve fiber area demonstrated in clinical trials, with sustained improvement in neuropathic pain. Significant nerve regeneration and metabolic improvements in Type 2 diabetes patients with peripheral neuropathy. Crosses blood-brain barrier to provide neuroprotection in stroke and traumatic brain injury models.

Anti Inflammatory

Well studied

Activates tissue-protective signaling pathways that reduce inflammation in multiple tissue types.

Tissue Repair

Early research

Studied for effects on tissue repair and wound healing through IRR activation in preclinical and clinical research.

Autoimmune

Early research

Modulates immune response through EPOR/β-common receptor complex without erythropoietic effects.

Dosage reference

Doses used in research
4 mg
Frequency in studies
Once daily
Handling
Reconstituted solution — research use only; not for administration
Timeline reported in studies
Initial effects: 7-14 days, Peak benefits: 4-6 weeks, Sustained effects: 6+ months
Storage
Powder: -80°C long-term, 4°C medium-term; Reconstituted: use immediately or refrigerate up to 24 hours
Cycle length
28 days standard protocol
Break between cycles
Variable based on indication, clinical trials used single 28-day cycles

Interactions

This list shows which other tissue-protective peptides and compounds researchers study alongside Ara 290, and flags pairings that call for extra caution in a research setting.

BPC-157 — synergistic TB-500 — synergistic Thymosin Beta-4 — compatible EPO (Erythropoietin) — compatible NAD+ — compatible Semaglutide — compatible Growth Hormone — compatible Anti-TNF Biologics — compatible

Reconstitution & storage

This is the standard laboratory method for turning freeze-dried Ara 290 powder into a liquid research solution, with extra care for light exposure.

  1. Allow vial to reach room temperature (15-20 minutes)
  2. Clean vial top with alcohol swab
  3. Slowly inject 1 mL sterile water into vial
  4. Gently swirl to dissolve (do not shake vigorously)
  5. Solution may appear slightly cloudy - this is normal
  6. Store the reconstituted solution refrigerated (2–8°C), labeled with the date and concentration, for laboratory research use only.

Lyophilized: -80°C long-term, 4°C medium-term, use within Extended when frozen

Reconstituted: 2-6°C, use within Up to 24 hours; use immediately when possible

Open the Ara 290 reconstitution calculator

Quality indicators

These are the manufacturing and lab-report checks researchers use to confirm an Ara 290 sample is pure and correctly identified — a quick sanity check against the Certificate of Analysis (COA), not a guarantee.

Pharmaceutical grade manufacturing - Clinical trial material manufactured under GMP conditions with full quality documentation

Proper peptide sequence verification - Correct 11-amino acid sequence (pGlu-Glu-Leu-Glu-Arg-Ala-Leu-Asn-Ser-Ser) with N-terminal pyroglutamate

Sterile lyophilized powder - Proper freeze-drying with excipients like sucrose or mannitol for stability and sterility

Light-sensitive formulation - Requires protection from light during storage, reconstitution, and administration

Clinical batch documentation - Certificates of analysis showing purity >95%, endotoxin levels <1 EU/mg, and sterility testing

Cloudy or discolored solution - Reconstituted solution should be clear to slightly cloudy and colorless - discoloration indicates degradation

What to expect

This timeline summarizes what the clinical trial literature reports at each study stage — research context for comparing studies, not a personal-results promise.

Week 1-2

Initial anti-inflammatory effects, potential mild improvement in pain symptoms

Week 2-4

Progressive nerve regeneration, improved tissue healing markers, enhanced wound healing if applicable

Week 4-6

Peak therapeutic effects, maximum nerve fiber density improvements, sustained pain relief

Month 2-6

Long-lasting benefits continue due to "molecular switch" effect, sustained tissue protection

Safety notes

This section covers Ara 290's regulatory status and handling notes — including its Orphan Drug designation and the medications it should not be studied alongside — reference context for laboratory researchers, not medical guidance.

  • Contraindicated with recent anti-TNF therapy (within 6 months) or EPO use (within 2 months)
  • Not recommended during pregnancy or in patients with BMI >34 kg/m²
  • Monitor for injection site reactions and rotate injection sites
  • Not FDA-approved; holds FDA Orphan Drug status for several indications
  • No anti-drug antibodies detected in human studies
  • No hematopoietic effects or risk of polycythemia unlike erythropoietin

Regulatory status

  • Not approved by the FDA for any indication.
  • Supplied and described for laboratory research use only — not for human or veterinary use.

Community data

Community Poll

How would you rate your overall experience with this peptide?

1284 votes · Community data

Community Insights

82%reported positive results
68%noticed effects within 2 weeks
91%would recommend to others

Based on data the community reported. Not clinical proof.

References

  1. Human islets (in vitro) · 100 nM · 48 hours

    Ara 290 protection against inflammatory damage in human pancreatic islets, supporting potential in diabetes treatment and transplantation.

  2. Human (9 patients) · 4 mg SC daily · 12 weeks

    Good safety profile and improved patient-reported outcomes in diabetic macular edema.

  3. Human (64 patients) · 1-8 mg SC daily · 28 days

    23% increase in corneal nerve fiber area at 4 mg dose in sarcoidosis-associated small fiber neuropathy. Significant nerve regeneration and pain reduction in moderate-severe cases.