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FOXO4-DRI (10 mg)
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ARA 290 Peptide (15mg)

$46.00

ARA 290 peptide represents a promising therapeutic peptide with demonstrated benefits in clinical studies of diabetic neuropathy and chronic neuropathic pain.

Description

ARA 290 Peptide

ARA 290 peptide is a synthetic 11-amino acid peptide derived from the tissue-protective domain of erythropoietin (EPO), specifically engineered to retain neuroprotective and tissue-protective properties while eliminating erythropoietic activity. This innovative therapeutic agent activates the innate repair receptor (IRR), also known as the common β-receptor (CD131), which plays a crucial role in tissue protection, repair, and regeneration processes.

Chemical structure & Properties

  • Molecular Formula: C59H95N17O22
  • Molecular Weight: 1,382 Da
  • Sequence: 11 amino acids derived from erythropoietin’s tissue-protective domain
  • Half-life: Approximately 6-8 hours following subcutaneous administration
  • Stability: Stable in lyophilized form, requires refrigeration when reconstituted

Key Highlights

  • Mechanism of Action: Selectively activates the Innate Repair Receptor (IRR / CD131), initiating cell survival pathways, lowering inflammation, and building cellular resilience against oxidative and hyperglycemic damage.

Clinical Applications and Research Benefits

Neurological Applications

Diabetic Neuropathy: Clinical studies demonstrate ARA-290’s efficacy in treating:

  • Peripheral diabetic neuropathy with significant pain reduction
  • Improvement in nerve conduction velocities and sensory function
  • Enhanced quality of life measures and functional capacity
  • Reduction in diabetes-related complications

Mechanism: ARA 290 peptide protects against hyperglycemia-induced neural damage, promotes nerve regeneration, and improves microvascular circulation to peripheral nerves.

Chronic Neuropathic Pain: Research indicates potential benefits in:

  • Sarcoidosis-associated neuropathy with 40% average pain reduction
  • Post-herpetic neuralgia and viral-induced neuropathy
  • Chemotherapy-induced peripheral neuropathy
  • Complex regional pain syndrome

Regulatory Disclaimer: ARA 290 peptide is an investigational peptide without FDA or EMA approval. The following data reflects Phase II research parameters, not medical guidelines.

Clinical Trial Dosing Protocols

Protocol Type Dose & Route Duration Primary Indications Studied
Pivotal Phase II (Standard)

4 mg (4,000 mcg) / day

 

(Subcutaneous)

28 consecutive days Diabetic neuropathy, Sarcoidosis small-fiber neuropathy
Extended Phase II

4 mg / day

 

(Subcutaneous)

Up to 12 weeks Diabetic macular edema
Early Pilot Studies

2 mg

 

(IV, 3x / week)

4 weeks Small-fiber neuropa
  • Route Rationale: 4 mg SC daily achieves tissue receptor (IRR) binding levels comparable to IV administration, making SC the preferred delivery route for outpatient clinical research.

Administration & Handling Guidelines

  • Injection Sites: Subcutaneous rotation across the abdomen, anterior thighs, or upper arms.

  • Reconstitution: Reconstitute lyophilized powder using sterile or bacteriostatic water.

  • Storage & Stability: Keep reconstituted solutions refrigerated at 2°C–8°C (36°F–46°F); use within 30 days.

Conclusion

ARA 290 peptide represents a promising therapeutic peptide with demonstrated benefits in clinical studies of diabetic neuropathy and chronic neuropathic pain. Its unique mechanism of action through innate repair receptor activation offers distinct advantages in neurological applications without the cardiovascular risks associated with traditional erythropoietin therapy.

The current evidence base includes positive Phase II clinical trial results with excellent safety profiles. However, the investigational status and need for Phase III studies necessitate careful consideration and medical supervision for any therapeutic application. Patients interested in ARA-290 therapy should engage in thorough discussions with qualified healthcare providers and explore participation in clinical trials or expanded access programs.

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