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

Suprefort (pancreas peptide complex): what the evidence says

At a glance

What it is: an oral capsule product sold as one of the Khavinson "Cytomax" natural peptide complexes, said to be extracted from young animal pancreas (product code A-1). UNVERIFIED the product code, the source tissue and the manufacturing method; these come from Nova's spec and seller descriptions, not from a primary source we could open.

What the evidence says: a PubMed search on Oct 27, 2026 found no study naming Suprefort. The closest records concern the synthetic tetrapeptide pancragen, such as a pancreatic-cell culture study; that is a different product. R1

Biggest risks: unknown. Animal-tissue extracts carry a theoretical risk of allergy and contamination, and the contents of a given capsule are not standardized. UNVERIFIED no safety data were found.

Rating

Human Human evidence None found
Animal Animal / lab evidence Only related Khavinson-group reviews R1
Regulatory Not FDA-approved · not on FDA's 503A or 503B bulk-substance category lists and not on FDA's compounding safety-risk page R2, R3, R4 · not named by WADA R5
Established human dose No

Evidence verdict: Any health use: Unknown (no peer-reviewed human trial found naming this product)

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: there is nothing specific to this product to grade. Claims for it rest on the wider Khavinson peptide-bioregulator literature, which comes mostly from one research group in St. Petersburg and has not been independently replicated in Western randomized trials.

What is it?

A dietary-supplement-style capsule of a tissue-derived peptide mixture, marketed alongside the synthetic tetrapeptide pancragen. Related pages: pancragen.

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
No study found — — — — No PubMed record names this product (searched Oct 27, 2026) —

Full reference list (PubMed, CT.gov, FDA and WADA checked Oct 27, 2026)

  1. R1 Khavinson VKh, et al. Bull Exp Biol Med. 2013. PMID 23486591
  2. R2 FDA, 503A bulk drug substances categories list (updated May 14, 2026). https://www.fda.gov/media/94155/download
  3. R3 FDA, 503B bulk drug substances categories list (updated Mar 21, 2025). https://www.fda.gov/media/94164/download
  4. R4 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
  5. R5 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 Suprefort (pancreas peptide complex). 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).