Neurological & CognitiveInvestigational (Phase 2)S

ARA-290

Cibinetide

Non-erythropoietic peptide studied for neuropathic and inflammatory indications.

Observational report only — live community data. Not medical advice. Does not recommend doses, protocols, or treatments.
Studies cited
2
Research grade
S
Community score
233

Trend index

Trackers
4,868

Overview

About ARA-290

Non-erythropoietic peptide studied for neuropathic and inflammatory indications.

Category
Neurological & Cognitive
Regulatory status
Investigational (Phase 2)
Also known as
Cibinetide
Self-reports
6

Community

What 6 users report

6 community reports

Positive 33% · Neutral 67% · Negative 0%

Most reported benefits

Appetite
6

Most reported side effects

Injection site irritation
4

Dose distribution

Median: 2000+ mcg · Most common: 2000+ mcg

0–25
0
25–50
0
50–100
0
100–200
0
200–400
0
400–600
0
600–1000
0
1000–2000
0
2000+
6

Commonly stacked with

Research

Cited research (1)

PubMed

ARA 290, a nonerythropoietic peptide engineered from erythropoietin, improves neuropathic symptoms in patients with sarcoidosis

Dahan et al., 2013

Source
Wiki study page →

Help

Frequently asked

What do PeptIQ users report about ARA-290?

This page summarizes 6 anonymized self-reports from PeptIQ users who track ARA-290, including commonly reported effects and co-tracked peptides. These are observational patterns, not clinical outcomes.

What research is cited for ARA-290?

1 sources are linked on this page, including PubMed articles, clinical trial registries, and FDA labels where applicable. Citations describe published research — not recommendations.

Is ARA-290 safe to use?

This wiki does not assess safety or recommend use. ARA-290 is listed as Investigational (Phase 2). Consult a licensed clinician for personal medical decisions.

What are the purported benefits and uses of ARA-290?

Research, primarily in animal models, suggests ARA-290 may have a wide range of therapeutic potentials due to its ability to promote angiogenesis (formation of new blood vessels), stimulate collagen synthesis, and modulate inflammatory responses.

Source

What is the legal status of ARA-290?

ARA-290 is not approved by the FDA for any human use. There is no legal basis for selling it as a drug, food, or dietary supplement in the United States. The FDA has classified ARA-290 as a Category 2 bulk drug substance, which explicitly prohibits licensed compounding pharmacies from using it in compounded medications.

Source

What are the known or theoretical side effects and risks of ARA-290?

The safety and effectiveness of ARA-290 have not been thoroughly evaluated in humans through rigorous clinical trials. This lack of human data means that safe dosages, short-term side effects, and long-term health consequences are largely unknown.

Source

What is the current state of research on ARA-290?

While there are over 200 published studies on ARA-290, the vast majority are animal or in vitro (cell) studies. These preclinical studies consistently show positive results across various tissue types. However, there is a significant lack of comprehensive human clinical trial data.

Source