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Recovery / Nerve Protocol

ARA-290 · 5ML

ARA-290 is a non-erythropoietic EPO receptor agonist studied for neuroprotection, anti-inflammation, tissue repair, and peripheral nerve recovery. Physician-reviewed. Prescription required.

Recovery Neuroprotection Prescription Required
What It Is
ARA-2905ML

Mechanism of Action

ARA-290 is a synthetic peptide derived from the tissue-protective region of Erythropoietin. It was designed to retain EPO's cytoprotective and anti-inflammatory effects without stimulating red blood cell production. Its mechanisms involve activation of a distinct receptor complex that triggers tissue protection, anti-inflammation, and repair pathways.

This selectivity allows ARA-290 to deliver cytoprotective, anti-inflammatory, and repair-promoting effects without the hematopoietic side effects of full EPO. It has been studied in neuropathic pain, sarcoidosis, and tissue protection contexts. Individual outcomes may differ. This protocol is not intended to diagnose, treat, cure, or prevent any disease.

Mechanism Biological Effect
Activation of tissue-protective EPO receptor subunits Cytoprotection without erythropoiesis
Anti-inflammatory signaling Reduced cytokines & immune activation
Anti-apoptotic pathways (PI3K/Akt) Enhanced cell survival
Immunomodulation Lower chronic inflammation
Endothelial support Improved microvascular function
Repair/regeneration signals Tissue recovery
Candidate Profile

Who It's Designed For

Your physician will determine eligibility based on your complete health intake. The following profiles are commonly associated with ARA-290 protocol candidates in clinical practice:

Neuropathic Pain

Individuals with physician-confirmed neuropathic pain where ARA-290's TPR activation may be clinically relevant.

Nerve Recovery

Individuals recovering from peripheral nerve injury or damage under physician supervision.

Inflammatory Conditions

Individuals with chronic inflammatory conditions where non-erythropoietic EPO receptor activation may support tissue protection.

Recovery Protocol

Individuals with tissue damage or vascular compromise seeking physician-supervised cytoprotective support.

Determine your candidacy

A physician will review your intake and make eligibility determination within 24–48 hours.

Begin Your Protocol
Outcomes & Timeline

What the Clinical Literature Indicates

All outcome language below reflects what has been observed in clinical and preclinical settings. Individual outcomes may differ significantly. These are not guarantees.

Weeks 1–4
Early-stage signaling activity may be observed. Individual outcomes may differ. Physician monitoring recommended.
Weeks 4–8
In clinical and preclinical settings, progressive effects have been associated with continued administration. Results vary by individual.
Weeks 8–12
Sustained physician-supervised administration may support continued outcomes. Your physician will evaluate protocol continuation.
Dosing Overview

Protocol Structure

Dosing is determined individually by your assigned physician. The following represents typical ranges discussed in clinical literature. Do not self-administer or adjust dosing without physician guidance.

Typical Range

4 mg 3x/week

Administration

Subcutaneous injection

Duration

4–12 weeks (physician-determined)

Frequency

3x weekly (physician-determined)

These ranges are indicative only. Your physician will prescribe the specific dose and schedule appropriate for your clinical profile.

What's Included

Your Protocol Package

Physician consultation — Virtual intake review and protocol consultation with your assigned NP/MD

Valid prescription — Issued by your attending physician upon protocol approval

Pharmacy-dispensed compound — Dispensed by our licensed 503A compounding pharmacy partner

Follow-up check-in — Physician review at protocol midpoint; reorder pathway established

Clinical Considerations

Contraindications & Safety Notes

Your physician will review your complete health history before determining eligibility. The following are commonly reviewed clinical considerations.

History of thrombosis: EPO receptor activity reviewed carefully in thrombosis history contexts. Full disclosure required.
Pregnancy or lactation: Not indicated. Contraindicated.
Hematologic conditions: EPO receptor agonists reviewed carefully in polycythemia or clotting disorder contexts.
Current medications: Disclose all medications at intake.
FAQ

Common Questions

This compound is not FDA-approved as a drug. It is dispensed as a compounded medication through licensed 503A compounding pharmacies operating under FDA guidelines. All Verum Health protocols require a valid physician prescription.
After completing your HIPAA-secure health intake, a physician or NP will review your medical history, current medications, goals, and contraindications. If you're a candidate, a virtual consultation is scheduled — typically 15–20 minutes. Turnaround is 24–48 hours from intake submission.
Protocol stacking is reviewed on a case-by-case basis during your physician consultation. Any combination protocol is evaluated for safety and clinical appropriateness. Do not combine protocols without explicit physician guidance.
Reorders are managed through your patient portal. A follow-up physician check-in is required at protocol completion before continuation is authorized. Reorder notification is sent 10 days before your protocol completes.

Begin your ARA-290 protocol.

Complete your intake. Physician review within 24–48 hours.

Recovery / Nerve Protocol

ARA-290

Physician-reviewed. Pharmacy-dispensed. Prescription required before any order is fulfilled.


Typical range4 mg 3x/week
Duration4–12 weeks
Intake to Rx24–48 hours
Pharmacy503A Licensed

Begin Your Protocol
Starting price$160
4-Month Refills Included
Approved protocols include 4 months of refills. Auto-refill available after initial physician approval.
Request a Consultation

Prescription required. Results may vary. Individual outcomes may differ.

Frequently Asked Questions

What is ARA-290 used for?

ARA-290 (Cibinetide) is a tissue-protective peptide studied for neuropathic pain, small fiber neuropathy, and metabolic conditions. It activates the innate repair receptor (IRR) to reduce inflammation and promote tissue healing.

What conditions may benefit from ARA-290?

ARA-290 has been studied for peripheral neuropathy, sarcoidosis-related neuropathy, diabetic neuropathy, and metabolic syndrome. It is used off-label for pain and nerve repair.

Is ARA-290 safe?

ARA-290 has a favorable safety profile in clinical studies. As with all peptide protocols at Verum Health, it is prescribed and monitored by a licensed physician.

How is ARA-290 administered?

ARA-290 is available as a subcutaneous injectable at Verum Health. Protocol length and dosing are determined by your physician based on your condition and goals.