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Prostamax

Aliases: Lys-Glu-Asp-Pro

Last verified: 2026-09-23

Research chemicalLimited evidenceBioregulatorsLow interest

The short version

A prostate tetrapeptide — normalization of prostatic function and microcirculation; part of Russian "peptide" urology. Key fact: Human data are limited: small trials or case-series reports exist, without large randomized studies. Preclinical and small clinical series. Status: research chemical. Not approved in the West.

Identity & type

Molecular type
bioregulator
Origin
A prostate tetrapeptide — normalization of prostatic function and microcirculation; part of Russian "peptide" urology.

Mechanism of action

Gene-regulatory action on prostate cells; anti-inflammatory.

not confirmed in humans

Dosing & routes

Official / clinical context

No approved official document exists for Prostamax. Any protocols mentioned are to be read as information, not as a recommendation.

Regulator-approved labeling and published study designs — never a recommendation.

Community-reported practice

1–5 mg/day SC in courses. A prostate bioregulator: users report less nocturia and improved urinary flow; all anecdotal.

Unverified self-reports. Not medical advice. Not endorsement.

Expected effects (community)

A prostate bioregulator: users report less nocturia and improved urinary flow; all anecdotal.

Protocol — official vs community

Official / label

No approved protocol exists. Prostamax is a research peptide bioregulator with no registered drug product in any major market.

Duration:

Preclinical and small clinical series in Russian 'peptide urology'; no large randomized trials.

Community (anecdotal)

1–5 mg SC daily for 10–20 days.

Cycle:
1–2 courses per year.
Break:
Months between courses.

The regimen is the shared Khavinson course pattern; only the prostate-function targeting claim distinguishes it from the rest of the series.

Human evidence

Human data are limited: small trials or case-series reports exist, without large randomized studies. Preclinical and small clinical series.

Preclinical evidence

Preclinical and small clinical series.

Known risks

  • None reported.characterized
  • Unregulated injectable supply — sterility, purity and accurate dose not assuredtheoretical

Teal: characterized in clinical/labeling contexts. Amber: theoretical or reported outside controlled settings.

Unknowns & evidence gaps

  • Long-term human safety
  • Optimal dose and pharmacokinetics

Frequently asked questions

References

Systematic references are being expanded; verify sources directly before any decision.