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Prostamax

Also called KEDP; Lys-Glu-Asp-Pro

A four-amino-acid bioregulator peptide studied in prostate tissue and cellular-aging experiments. It is not an established treatment for prostatitis or an enlarged prostate.

Overview

What it is

A synthetic tetrapeptide of lysine, glutamic acid, aspartic acid and proline.

How it works

In cells from donors aged 75 to 86, it loosened DNA packaging (chromatin). That is not DNA repair or reversed aging.

What the research shows

In 60 rats with induced non-bacterial prostate inflammation, it reduced swelling and inflammatory cells, but prostate size did not change significantly. A Russian patent describes improvements in 35 prostatitis and 19 prostate adenoma patients, without randomization or blinding.

Studied for

  • Prostate inflammationrats
  • Chromatin in older donors' cellslab
  • Prostatitis and BPHpatent reports

Safety and regulatory status

Safety and side effects

No reliable human side-effect, interaction or long-term data. Do not stop prescribed prostate treatment. Seek prompt care for inability to urinate, blood in urine, severe lower abdominal pain, or painful urination with fever.

Regulatory status

Not approved by the FDA for any use.

Mixing and dosing reference

Reference information only. Read before using this section.
Reference information only. Not instructions. These mixing and dosing figures summarize published studies and third-party protocols so you can understand the research. They are not medical advice, not a recommendation that anyone use any substance, and not a treatment plan. They do not apply to Research Products, which are for laboratory research only and must never be used in humans or animals. Never self-administer any compound. Only a licensed healthcare professional who has evaluated you can decide whether a medication is appropriate and how it should be used.

Prostamax (20 mg Vial) Dosage Protocol

Vial
20 mg Prostamax
Add diluent
2 mL
Concentration
10 mg/mL
1 unit (U-100)
100 mcg in 0.01 mL
Route
Intramuscular
How often
Once per day (intramuscular).
Typical range
500 mcg–1 mg once daily (gradual titration).
Cycle length
8–12 weeks; optional extension to 16 weeks.

Standard / Gradual Approach

Phase / WeekDaily Dose (mcg / mg)Units (per injection) (mL)
Weeks 1–2500 mcg (0.5 mg)5 units (0.05 mL)
Weeks 3–4750 mcg (0.75 mg)7.5 units (0.075 mL)
Weeks 5–81,000 mcg (1 mg)10 units (0.10 mL)
Weeks 9–12 (optional extension)1,000 mcg (1 mg)10 units (0.10 mL)

How to mix

  1. Draw 2.0 mL bacteriostatic water with a sterile syringe.
  2. Inject slowly down the vial wall; avoid foaming.
  3. Gently swirl/roll until dissolved (do not shake).
  4. Label and refrigerate at 2–8 °C (35.6–46.4 °F), protected from light; follow product-specific use-by instructions.
Dosing details
  • Start: 500 mcg (0.5 mg) daily; increase by ~250 mcg every 2 weeks as tolerated.
  • Target: 1 mg daily by Weeks 5–8.
  • Frequency: Once per day (intramuscular).
  • Cycle Length: 8–12 weeks; optional extension to 16 weeks.
  • Timing: Any consistent time; rotate injection sites among large muscle groups.
Storage
  • Lyophilized: Follow the exact product’s labeled storage temperature and expiration instructions; keep the vial dry and protected from light.
  • Temperature changes: Do not assume refrigeration or freezing extends a product’s expiration date without validated evidence.
  • Reconstituted: Refrigerate at 2–8 °C (35.6–46.4 °F); follow product-specific use-by instructions and avoid freeze–thaw cycles.
  • Allow vials to reach room temperature before opening to reduce condensation uptake.
Administration technique
  • Intramuscular administration guidance from clinical best‑practice resources.
  • Clean the vial stopper and skin with alcohol; allow to dry completely.
  • For IM injection, use a 22–25 gauge, 1–1.5 inch needle inserted at 90° into a large muscle (deltoid, vastus lateralis, or gluteus).
  • Aspiration before IM injection is no longer routinely recommended for most sites.
  • Inject slowly and steadily; wait briefly before withdrawing.
  • Rotate sites systematically to avoid muscle irritation or fibrosis.
  • Alternative (SC): If subcutaneous route is preferred, use a 23–25 gauge, 5/8 inch needle at 45° into fatty tissue.
Important notes
  • Use new sterile insulin syringes or appropriate IM syringes; dispose in a sharps container.
  • Rotate injection sites among large muscle groups (deltoid, vastus lateralis, gluteus) to reduce local irritation.
  • Inject slowly; wait a few seconds before withdrawing the needle.
  • For volumes ≤10 units, use 30‑ or 50‑unit syringes for better precision.
  • Document daily dose and site rotation to maintain consistency.

Protocol source: PeptideDosages.com

Common questions

Does Prostamax shrink the prostate?

Not shown; prostate size did not change significantly in the rat study.

Do human-cell studies mean it works in people?

No. They show biological activity, not patient benefit.

Is prostatitis the same as BPH?

No. One is inflammation, the other is non-cancerous enlargement.

Related in Hormones and Reproductive Health

Sources and further reading (4)
  1. Dzhokhadze TA, et al. KEDP and chromatin in older-donor cells. Georgian Med News, 2012.
  2. Borovskaya TG, et al. Prostamax in experimental chronic aseptic prostatitis. Mod Res Inflamm, 2013.
  3. NIDDK. Prostatitis; Enlarged prostate (BPH).
  4. Source summary: PeptideDosages.com research overview (rewritten for NVO).
Educational information only. This content summarizes published research for general education. It is not medical advice, not a recommendation to use any substance, and not an instruction for human or animal use. It does not describe any Research Product sold on this site.