Evidence review: Open Peptide Project (verified against primary PubMed, ClinicalTrials.gov & FDA records) · Last checked 2026-10-27. ← Back to Evidence Library

Gepon (Human Ezrin Peptide 1, HEP-1): what the evidence says

At a glance

What it is: a 14-amino-acid peptide (TEKKRRETVEREKE) from the hinge region of human ezrin, registered for human use in Russia since 2001 under the brand Gepon. R1, R2

What the evidence says: a review by its developers says it treats and prevents mucosal candidiasis, herpes zoster and infection-related diarrhea in people with HIV. R1 It reduced colitis in mice. R3

Biggest risks: unknown; no independent safety data found.

Rating

Human Human evidence Limited: clinical claims in a developer-authored review R1; small COVID-19 trial with no results R4
Animal Animal / lab evidence Mouse colitis, fibroblast studies R3, R2
Regulatory Not FDA-approved · not on FDA's 503A or 503B bulk-substance category lists and not on FDA's compounding safety-risk page R5, R6, R7 · not named by WADA R8
Established human dose No

Evidence verdict: Opportunistic infections in HIV: Limited (Russian clinical reports, reviewed by the developers) · Colitis/wound repair: animal and lab only

This page reports what studies used. It is not dosing advice.

Legend: HUMAN data · ANIMAL / LAB data · UNKNOWN · UNVERIFIED: not yet confirmed against a primary source

About the evidence: the human claims come mainly from a review written by the peptide's developers, which is a conflict of interest. UNVERIFIED the underlying Russian clinical publications.

What is it?

Related pages: LL-37, Thymosin alpha-1, KPV.

Does it work?

Is it safe?

Gray-market vials: extra risks

A gray-market vial has no quality control and no guarantee of identity, strength or sterility. We test retail vials blind under the Open Peptide Standard; see /tests/. A passing test covers one batch on one date and does not mean the compound is safe.

Is it legal?

Study details
Study details

These are amounts researchers used, not recommendations.

Study People / model Route Amount used Follow-up Reported Citation
Chulkina 2020 Mouse DSS colitis IP Per study Per study Less colitis PMID 32621844

Full reference list (PubMed, CT.gov, FDA and WADA checked Oct 26, 2026)

  1. R1 Holms RD, et al. Int J Mol Sci. 2021. PMID 34769119
  2. R2 Chulkina M, et al. Eur J Pharmacol. 2017. PMID 28668507
  3. R3 Chulkina MM, et al. Peptides. 2020. PMID 32621844
  4. R4 ClinicalTrials.gov NCT04627233, Shahid Beheshti University phase 1 HEP-1 COVID-19 trial, n = 20 estimated, status unknown, no results posted (CT.gov API v2, checked Oct 26, 2026). https://clinicaltrials.gov/study/NCT04627233
  5. R5 FDA, 503A bulk drug substances categories list (updated May 14, 2026). https://www.fda.gov/media/94155/download
  6. R6 FDA, 503B bulk drug substances categories list (updated Mar 21, 2025). https://www.fda.gov/media/94164/download
  7. R7 FDA, Certain bulk drug substances for use in compounding that may present significant safety risks (content current Apr 22, 2026). https://www.fda.gov/drugs/human-drug-compounding/certain-bulk-drug-substances-use-compounding-may-present-significant-safety-risks
  8. R8 WADA. The 2026 Prohibited List, full list checked; compound not named. https://www.wada-ama.org/sites/default/files/2025-09/2026list_en_final_clean_september_2025.pdf

Disclaimer

This page is for education and harm reduction, not medical advice or a recommendation to use Gepon (Human Ezrin Peptide 1, HEP-1). This compound is not FDA-approved. Any product sold under this name in the US is unregulated. Report problems to FDA MedWatch (https://www.fda.gov/safety/medwatch).