ImmuneInvestigationalEvidence tier: Human RCT

ARA-290 (Cibinetide)

Last updated October 21, 2026. Approval line checked October 21, 2026. No compounding source date is assigned.

FDA status

Investigational

Investigational. No FDA-approved cibinetide product is recorded for this entry. It has been studied in clinical trials.

ClinicalTrials.gov: cibinetide

Evidence tier

Human RCT. The tier is the highest indexed study type. It is not a safety rating and it is not an FDA approval. Confidence score 4/5. 59 PubMed citations indexed.

ARA-290 (Cibinetide) in the literature

ARA-290 is an 11-amino-acid non-hematopoietic peptide engineered from the helix B surface domain of erythropoietin that selectively activates a heterodimeric innate repair receptor (EPOR/β-common rece

What the literature studies

Immune Research

Evidence tier

Human RCT

Compounding record

Status not verified

Confidence
4/5

Regulatory record

Status not verified. No product-specific FDA primary source is recorded for this entry. FDA approval and compounding eligibility are not verified. Research information is not evidence of FDA approval. Approval, where applicable, is specific to a drug product, indication and route. Research information is not evidence of FDA approval. Approval, where applicable, is specific to a drug product, indication and route.

Regulatory source not verified; no checked date is assigned.

Regulatory context and verification limits are documented below.

Questions

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