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

Vialox (pentapeptide-3, GPRPA): what the evidence says

At a glance

What it is: a synthetic pentapeptide (Gly-Pro-Arg-Pro-Ala) sold in "Botox-like" wrinkle serums as a nicotinic acetylcholine receptor blocker. UNVERIFIED the receptor mechanism; it comes from supplier material.

What the evidence says: we found no independent, peer-reviewed randomized trial of this ingredient on its own. Claims mostly come from ingredient suppliers.

Biggest risks: topical use is generally low-risk; injecting it has no safety data at all.

Rating

Human Human evidence Very limited (topical only)
Animal Animal / lab evidence Supplier and lab data (not peer-reviewed) UNVERIFIED
Regulatory Cosmetic ingredient, not a drug · not on FDA's 503A or 503B bulk-substance category lists and not on FDA's compounding safety-risk page R1, R2, R3 · not named by WADA R4
Established human dose No

Evidence verdict: Wrinkles (topical): Unknown (no peer-reviewed study found) · Injection: Unknown (zero human data)

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: cosmetic-peptide studies are usually small, short, funded by the maker and test blends rather than one ingredient. A general dermatology review notes that cosmeceutical peptides are not tested as rigorously as drugs. R5

What is it?

Related pages: syn-ake, argireline, snap-8, leuphasyl.

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 dosing studies — Topical Cosmetic concentrations not reviewed — — —

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

  1. R1 FDA, 503A bulk drug substances categories list (updated May 14, 2026). https://www.fda.gov/media/94155/download
  2. R2 FDA, 503B bulk drug substances categories list (updated Mar 21, 2025). https://www.fda.gov/media/94164/download
  3. R3 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
  4. R4 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
  5. R5 Lupo MP, et al. Dermatol Ther. 2007. PMID 18045359

Disclaimer

This page is for education and harm reduction, not medical advice or a recommendation to use Vialox (pentapeptide-3, GPRPA). This is a cosmetic ingredient. Injecting cosmetic peptides has no human safety data. Report problems to FDA MedWatch (https://www.fda.gov/safety/medwatch).