In this guide
What is Prostamax?
Prostamax is a lab-made peptide, a short chain of four amino acids, that people inject hoping to help an enlarged prostate, chronic prostatitis or urinary symptoms such as a weak stream and waking at night to urinate.
It comes from a Russian research program led by Vladimir Khavinson, whose group calls these short peptides bioregulators and names each one after the organ it is meant to target. The group's 2001 patent describes the chain lysine, glutamic acid, aspartic acid and proline, written Lys-Glu-Asp-Pro or KEDP, with the formula C20H33N5O9 and a molecular weight of about 487.5. The patent presents it as a lab-made successor to Prostatilen, an older preparation extracted from animal prostate tissue. [1], [2], [3] The molecule studied in the published papers is the “free acid” form, H-Lys-Glu-Asp-Pro-OH, with no chemical cap on its end. [4]
The Russian company Geropharm and the Tomsk Institute of Pharmacology presented Prostamax in 2009 as a new peptide drug “in joint development”, and Geropharm's 2015 pipeline still listed it under urology. We found no registration, trial permit or later news. [5], [6] Today it is sold mostly as 20 mg vials of freeze-dried powder labeled for research, and the developer institute's own catalogue of lab-made peptide capsules does not include it. [7], [8] FDA told one US seller in June 2026 that its Prostamax is an unapproved new drug. [9]
The name covers several unrelated products. A registered medicine in Uzbekistan sold as Prostamax is a rectal suppository made from prostate extract. A Ukrainian capsule sold as Prostamax is a saw palmetto supplement. Libidon, often sold beside it, is a capsule of natural prostate peptides. None of them is the four-amino-acid peptide this guide covers. [10], [11], [12]

One name, several products
- Prostamax (KEDP) research vials and pens
- What it is: Lab-made Lys-Glu-Asp-Pro, 20 mg vials of powder or prefilled pensRoute: Injection: subcutaneous in practice; into a muscle in the patentWebsite schedule: Most often 500 mcg–1 mg once dailyHuman data: Patent case series only
- Italian blend (RESIFLEXIN Plus)
- What it is: Capsules listing KEDP, KEDG and KE (Vilon) with arginine and plant extractsKEDP amount: Not statedHuman data: None
- Not Prostamax (KEDP)
- “Prostamax” suppositories (Uzbekistan): Registered medicine: 50 mg prostate extract, rectal“Prostamax” capsules (Ukraine): Saw palmetto supplementLibidon: Natural prostate peptide complex (A-16), 10 mg per capsuleProstatilen: Preparation extracted from animal prostate tissue; the patent’s ‘prototype’
Amounts are as stated by each product; no public test shows what any research vial contains.
Only the lab-made KEDP peptide is Prostamax in this guide; the other products are different substances with their own evidence.
Typical Prostamax Protocols
| Example | Amount each time | Frequency | Total per day | Duration |
|---|---|---|---|---|
| Low | 100–200 mcg | Once daily | 100–200 mcg | 10–20 days, repeated every 3–6 months Described by its source as common anecdotal practice that has not been validated [13] |
| Mid | 750 mcg (0.75 mg) | Once daily | 750 mcg | 10–20 days Protocol website [14]; the same 750 mcg a day appears in public forum reports [16], [17] |
| High | 2 mg (2,000 mcg) | Once daily | 2 mg | 10 days, 2–3 courses a year with 4–6 months between A pen maker's protocol quoted by a Ukrainian seller: 20 clicks of 100 mcg [15] |
The most common pattern in the reviewed sources is 500 mcg to 1 mg once a day by injection. Sources split on how long to keep going: some describe a 10–20-day course repeated a few times a year, and a copied template describes a continuous 8–12-week run that steps up from 500 mcg (see the intramuscular table below). [14], [18], [7], [19], [20]
- Titration Changing the amount in steps
- Short-course pages use one fixed amount. The copied 8–12-week template starts at 500 mcg a day for two weeks, moves to 750 mcg for two weeks and then 1 mg. Another page starts at 500 mcg and raises it to 1 mg “based on tolerance”, and one goes on stepping up to 3 mg a day by week 7. No study has tested any of these steps. [19], [18], [21]
- Breaks and cycles
- Short courses are followed by a break: 3–6 months in two sources and 4–6 months in the pen protocol, so about 2–4 courses a year. The 8–12-week template does not describe a break. [13], [18], [15], [7]
- Timing
- Most pages give no time of day; one says any consistent time. Community education groups mention morning injections. [7]
Read the units: mcg means micrograms, and 1 mg equals 1,000 mcg. A 20 mg vial holds 20,000 mcg, so the vial size is a stock, not a dose. Each amount here is for one injection, and each schedule gives one injection a day, so the amount and the daily total are the same number. How mcg converts to syringe units.
Before you compare any of these numbers, four cautions. First, urinary symptoms and a raised PSA (prostate-specific antigen, a blood test used to check the prostate) can come from an enlarged prostate, infection or prostate cancer, so they need a medical check first; Prostamax has never been tested on PSA or cancer (see the risks). [22], [23] Second, do not stop or change prescribed prostate medicines on your own. Third, the men in the developers' patent examples received it into a muscle in amounts that were never reported one by one, and no side-effect collection was described, so the injected amounts in these tables are untested. [1] Fourth, a rat abstract suggests it can lower male-hormone activity, the opposite of what some “sexual function” marketing implies. [24]
Each row is a complete schedule from one source, so its amount and duration belong together. Low, mid and high are alternatives, not steps to move through. These schedules come from protocol websites and a seller's pen instructions rather than clinical trials; the cited references give the full details.
What about intramuscular injection, the route used in the patent?
| Example | Amount each time | Frequency | Total per day | Duration |
|---|---|---|---|---|
| Patent patient examples | 0.01–100 mcg per kg of body weight (0.7–7,000 mcg for a 70 kg man) | Once daily | 0.7–7,000 mcg at 70 kg | 10–40 days, depending on severity The inventors' human examples; individual doses were not reported [1] |
| Short course | 500 mcg, raised to 1 mg if tolerated | Once daily | 500 mcg–1 mg | 10–20 days, then 3–6 months off (2–4 courses a year) Protocol website [18] |
| Stepped course | 500 mcg (weeks 1–2), 750 mcg (weeks 3–4), then 1 mg | Once daily | 500 mcg–1 mg | 8–12 weeks Protocol website [19]; the same template is copied on several other pages [7], [25], [26], [27] |
The patent range is so wide (a 10,000-fold spread) that almost every website amount fits inside it. That makes it a boundary, not a guide: it does not say which amount any patient received or which amount worked. [1]
In community education groups, three traditions show up. The most common is roughly 500–750 mcg a day by subcutaneous injection for 30–60 days, repeated a few times a year. A second applies a general rule used for every bioregulator, 1–2 mg a day for 20–30 days, which one educator said was worked out from capsule products rather than injection studies. A third uses a short 10-day course once or twice a year. None of the educators cited a Prostamax dosing study, and their daily amounts differ about tenfold.
Where protocols differ: products, routes, units and course length ↓
Where these numbers come from
The subcutaneous rows each come from one source that publishes a complete schedule: PeptideInsight for the low row (100–200 mcg a day for 10–20 days, repeated every 3–6 months, described as anecdotal and not validated), Lux BioPure for the mid row (0.75 mg once daily for 10–20 days) and a Ukrainian seller quoting a pen maker's protocol for the high row (2 mg once daily for 10 days, 2–3 courses a year with 4–6-month breaks). [13], [14], [15]
The intramuscular table gives the patent's range, which the inventors used in their chronic prostatitis and prostate adenoma examples, then a short course from Peptides Institute and the stepped course from Peptides.ID. The same 500 → 750 → 1,000 mcg template, with the same syringe-unit arithmetic, appears on PeptideDosages (the earliest dated copy, first published in March 2026), PeptideDosing.ca, Research Protocols and Research Stacks, so it counts as one source copied several times. PeptideDosages calls the route subcutaneous in its introduction and intramuscular in its chart. [1], [18], [19], [7], [25], [26], [27]
Thirty-four dosing pages were compared and grouped by where their numbers seem to come from. The recurring 500 mcg–1 mg a day pattern is cross-checked by Lux BioPure, Peptides Institute and PeptideMind's summary card. [14], [18], [20]
Excluded from the typical comparison: oral amounts of 10–40 mg a day, because no capsule stating its Prostamax content could be traced; 5–10 mg a day for 10 days from a seller with no source; 1–5 mg a day for 10 days from a page that cites an unrelated study; a 12-week climb to 3 mg a day; a page that gives the wrong amino-acid sequence; and a summary that presents a rat dose as a human protocol. [28], [29], [30], [31], [21], [32], [33]
What is Prostamax commonly used for?
People usually look into Prostamax because of prostate symptoms: a weak or stop-start stream, dribbling, needing to go often, waking at night to urinate, or pelvic pain that has been called chronic prostatitis. In community education groups, most are men in their late 50s to 70s, and some want to protect the prostate as they age. A smaller group hopes it will lower a raised PSA.
The developers' patent describes the peptide as “regulating prostate functions” and tested it in chronic prostatitis and prostate adenoma, the older term for benign enlargement. FDA's 2026 warning letter quotes a seller's claims that it reduces prostate inflammation and helps BPH and bladder control. The sections below describe what was measured; they do not show that Prostamax treats or prevents any of these conditions. [2], [9]

An enlarged prostate (BPH) and urinary symptoms
Benign prostatic hyperplasia (BPH) is growth of the prostate that is not caused by cancer. It can make it hard to start or empty, weaken the stream and cause frequent, urgent or night-time urination, and it sometimes leads to urinary retention, where the bladder cannot empty. [22] The patent reports that 19 men with early-stage adenoma urinated faster and less often during the day after 10–40 days of injections, and a second company's patent reports that 16 men felt better on suppositories. Neither reported results for its comparison group or was published in a journal. See what those reports can and cannot show. [2], [34]
Approved medicines for BPH already exist, including alpha blockers, 5-alpha reductase inhibitors and the phosphodiesterase-5 inhibitor tadalafil. [22], [35]
Chronic prostatitis and pelvic pain
Prostatitis covers several conditions: chronic prostatitis or chronic pelvic pain syndrome, acute and chronic bacterial infection, and inflammation found by chance without symptoms. [36] The patent's larger example was 35 men aged 23–45 with chronic prostatitis who had not done well on usual treatment; it reports that pain disappeared in 64% and urination improved after 10–40 days. In rats, the peptide reduced scarring in a surgical prostatitis model and lowered an inflammation score in infected rats. [2], [37], [1]
Shrinking the prostate
The idea that Prostamax shrinks the prostate rests on two sources. In one rat study, glands enlarged with a drug (sulpiride) were 24% lighter and 40% smaller in volume after 60 days of the peptide, but the printed dose is a thousand times higher than the same group used a year earlier. The patent's prostatitis example says ultrasound showed a smaller prostate, without numbers. No study measured prostate size in men with BPH in a way that can be checked. [38], [2]
Lowering PSA
No study has measured Prostamax and PSA. Neither patent reports PSA. [2], [34] PSA can rise with BPH, prostatitis or cancer, and a product that lowered it would not show which one is present. Why that matters.
Sexual function and libido
Prostamax is often filed under “hormonal and sexual health”. The patent reports that sexual function improved in men with chronic prostatitis and that about 37% of men in each example noted better libido, but these were questionnaire answers without a comparison. [2] A rat abstract from the drug's developers found the opposite direction for hormones: smaller seminal vesicles, which the authors called an anti-androgenic effect. [24] See the hormone question.
Other uses you may come across
Some pages describe Prostamax as an anti-aging peptide because it loosened packed DNA in white blood cells from very old people, in the laboratory. Others claim it reduces prostate cancer risk, or cite “more than 10,000 patient-years” of safe use. We found no data for either claim. [39], [32], [40]
Where do Prostamax protocols differ?
The recurring 500 mcg–1 mg a day is easy to summarize. The disagreements start when a page mixes up products, routes or units. Here is what varies and why it matters.
Which Prostamax is the number for?
Check this first. The lab-made peptide is sold as 20 mg vials or prefilled pens. The Uzbek Prostamax is a 50 mg suppository of prostate extract, the Ukrainian Prostamax is saw palmetto, and Libidon capsules contain 10 mg of a natural prostate “peptide complex”. Their amounts cannot be compared with Prostamax amounts. [7], [15], [10], [11], [41] One page even prints the wrong sequence, Lys-Asp-Glu-Leu, and another shows an unrelated chain of amino acids. [32], [40]
Micrograms, milligrams and a thousandfold spread
Published daily amounts run from 100 mcg to 10 mg for injections and up to 40 mg a day for capsules that nobody could trace to a product. Even the research is inconsistent: the suppository patent gives 0.3–1.0 mg per suppository in its claim and 0.3–1.0 mcg in its patient example, and a 2014 rat study prints a dose a thousand times higher than the same group's 2013 study. [13], [30], [28], [34], [38], [37] The figure below puts the human and website numbers on one scale.

Daily amounts span more than 10,000-fold
From the developers' patents
- Patent patient range (70 kg man)
- 0.7–7,000 mcg a day for a 70 kg man (patent range, into a muscle).
- Suppository patent: example
- 0.3–1.0 mcg a day in the suppository patent example.
- Suppository patent: claim
- 300–1,000 mcg a day in the suppository patent claim.
1,000-fold conflict in the same patent.
From websites and sellers
- Website low (subcutaneous)
- 100–200 mcg a day (website low, subcutaneous).
- Most common website pattern
- 500–1,000 mcg a day (most common website pattern).
- Pen protocol
- 2,000 mcg (2 mg) a day (pen protocol).
- Seller claim (10 days)
- 5,000–10,000 mcg (5–10 mg) a day (seller claim, 10 days).
- Capsule claims (no traceable product)
- 10,000–40,000 mcg (10–40 mg) a day (capsule claims, no traceable product).
Animal doses are not shown and cannot be converted to human doses. Daily amounts; one injection a day unless stated.
Amounts cannot be compared across sources: they span more than 10,000-fold, and one patent contradicts itself 1,000-fold.
Is the number for one dose or the whole day?
5 mg twice a day is 10 mg for the day. Most pages give one daily injection, so the dose and the daily total match. Twice-daily use appears only in forum posts, including one person who reported 5 mg twice a day for 20 days. [42] Pens count in clicks: at 100 mcg a click, 20 clicks is 2 mg. [15]
Into a muscle or under the fat?
The inventors injected their patients into a muscle, and several websites say intramuscular only. Most forum users and community education groups use subcutaneous injection (into the fatty layer under the skin). Forum users argue about which works better, with no data either way. [2], [19], [43] How routes compare.
How many days, and how often is a course repeated?
Courses range from 10 days (pen protocol, several websites and one community education tradition) through 10–40 days (patent), 30–60 days (a community education tradition) to 8–12 weeks (the copied stepped template), and one member of a community education group reported about three months without a break. Repeats range from every 3–6 months to “2–3 courses a year”. [15], [1], [19], [18] These are conventions, not results from a trial comparing course lengths; nothing shows that a longer course works better.
Do sources start low and step up?
Some do. The copied template climbs from 500 to 1,000 mcg over four weeks, one page climbs to 3,000 mcg by week 7, and one page raises the amount by tolerance. Short-course pages and the pen protocol use one fixed amount. The only person-level titration we found in community education groups started at 500 mcg for three days, moved to 800 mcg a day and then to 1 mg every other day. [19], [21], [18], [15]
Are there capsules?
Many pages give capsule doses of 10–40 mg a day, and some say a Russian capsule holds about 20 mg of peptide. We could not find any such capsule: the developer institute's catalogue does not list Prostamax, and the prostate capsule it does sell, Libidon, is a natural extract. An Italian blend lists KEDP with two other peptides but does not state the amount. [28], [29], [44], [45], [8], [12], [46]
How do micrograms convert to syringe units?
Injection pages often give amounts as “units” on an insulin syringe. A U-100 syringe holds 100 units per millilitre, so units measure volume, not an amount of Prostamax. How much peptide each unit holds depends on how much water was added to the vial.
For example, a 20 mg vial mixed with 2 mL of water holds 10 mg per mL, so each unit holds 100 mcg: 500 mcg is 5 units, 750 mcg is 7.5 units and 1 mg is 10 units. This is the example the stepped template uses. The same 750 mcg from a 20 mg vial mixed with 3 mL is about 11 units. Doserly's reconstitution calculator works this out for any vial and shows each step. [7], [21]
Source-by-source comparison
Unit key: 1 milligram (mg) = 1,000 micrograms (mcg). A 20 mg vial mixed with 2 mL gives 10 mg per mL, or 100 mcg per syringe unit.
Stepped template (one lineage)
PeptideDosages, Peptides.ID, PeptideDosing.ca, Research Protocols and Research Stacks give 500 mcg in weeks 1–2, 750 mcg in weeks 3–4 and 1 mg from week 5, over 8–12 weeks, from a 20 mg vial with 2 mL. PeptideDosages calls the route subcutaneous in its introduction and intramuscular in its chart; Research Stacks also describes 10–20-day cycles that cannot contain its own 12-week table. In March 2026 PeptideDosages also listed 5–10 mg a day for 5–10 days; that line has since been removed. [7], [19], [25], [26], [27]
Short courses
PeptideInsight: 100–200 mcg a day under the fat for 10–20 days, repeated every 3–6 months. Lux BioPure: 0.75 mg a day for 10–20 days, or 0.5–1 mg a day. Peptides Institute: 500 mcg to 1 mg into a muscle for 10–20 days, 3–6 months off. The Peptide Catalog: about 1–2 mg a day for 10–20 days, described as self-reported community practice. CalcMyPeptide: 1–2 mg a day for about 10 days. A Ukrainian seller's pen: 2 mg a day for 10 days, 2–3 courses a year. Everything Peptide: 1–5 mg a day for 10 days. Celexir: 5–10 mg a day for 10 days. [13], [14], [18], [47], [48], [15], [31], [30]
Other schedules
Dosage Peptide: 500 mcg rising every two weeks to 3 mg a day in weeks 7–12. MyPeptideMatch: 200 mcg a day for 10 days, 4–6 months between courses. PeptideMind's card gives 500 mcg–1 mg a day, while its FAQ says 500 mcg to 20 mg, “most often cited around 10-20 mg daily”. Peptide Initiative repeats the patent's 0.01–100 mcg/kg. [21], [32], [20], [40]
Capsule claims
PeptaBase gives 20–40 mg a day by mouth; Peptide Database and Peptibase 10–20 mg a day; PeptScope says each capsule holds about 20 mg of peptide. None names a product with a label stating its Prostamax content. [28], [29], [45], [44]
Errors found
MyPeptideMatch prints the sequence as Lys-Asp-Glu-Leu. Peptide Initiative displays KGDG-KGDG-DLKDGA and claims “>10,000 patient-years” of follow-up without a source. Everything Peptide cites PubMed 21267487 as Prostamax research; it is a study of telomerase in HeLa cells. Peptide Database prints a molecular weight of 473 instead of 487.5. PeptideTrace lists the 2013 rat dose in its dosing summary. PeptideInfo and PeptideInsight say there is no human use, missing the patent's examples. [32], [40], [31], [29], [33], [49], [13]
What happens when you stop Prostamax?
No study has followed people after stopping. The patent says the effect was “prolonged” without giving a follow-up time, and no report describes withdrawal effects or a rebound. [2]
Public forum accounts point both ways, and each is one person:
- One user said the benefit of a 3-week course lasted about six months; he then started a prostate supplement. [16]
- Another, who also took tadalafil, said morning trickling came back soon after his 3-week course and he reordered. [16]
- In another thread, a user said his BPH symptoms returned when he ran out for several weeks. [43]
- A user whose PSA rose while taking it reported only a small fall, from about 15 to about 13, about six weeks after stopping, and said he would have it checked. [43]
The end of a course is a sensible time to review symptoms and any PSA results with a clinician, especially if any prescribed medicine was changed along the way.
Do injected and other forms of Prostamax behave the same way?
No one has measured this for any route. A subcutaneous injection is absorbed from the fatty layer under the skin; an intramuscular injection is absorbed from muscle, which usually has a richer blood supply. Those are different starting points, so the same amount by each route would not necessarily give the same exposure. For Prostamax, nobody has measured either one.
Bioavailability is how much of a dose reaches the blood in the form being measured. For Prostamax it is unknown for every route. Computer models from the developer's group predicted that the peptide could fit some transporter proteins in the gut and elsewhere, while another of their papers noted that it did not bind strongly to the transporter most common in prostate tissue. Predictions are not measurements of absorption. [50], [51]
How long does Prostamax last in the body?
Nobody knows. No study has measured its half-life, its blood levels or how quickly it is broken down, in people or animals. Pharmacokinetics, the study of how the body absorbs and clears a substance, has simply not been done for Prostamax.
What about suppositories, capsules and nasal sprays?
- Suppositories. A second Russian company patented a rectal suppository of the peptide in 2017 and reports 16 men with BPH; its unit conflict is described above. It is a patent, not a product we could find on sale. [34]
- Capsules. No capsule stating its Prostamax content could be verified, and an Italian blend does not state the amount. [8], [46]
- Nasal sprays and pens. One South African seller lists pens and nasal sprays; no data exist for either. [52]
Should it be injected near the prostate?
No source describes injecting near or into the prostate, and the patients in the patent received injections into a muscle elsewhere in the body. The idea that each bioregulator acts on its own organ comes from pieces of rat tissue grown in a dish, and in those experiments Prostamax also acted on brain and skin tissue. [2], [53], [54]
Free acid or amide: is every vial the same molecule?
The papers describe the free acid, H-Lys-Glu-Asp-Pro-OH, and the patent's synthesis example made its acetate salt. [4], [2] Research vials rarely state the form, and no public test shows what any vial contains or how much.
How should Prostamax be stored, and how long does it last?
There is no stability study for any Prostamax product. What exists are seller and website instructions:
- Powder, before mixing. Several pages say to keep the freeze-dried (lyophilized) powder frozen at −20 °C (−4 °F) for long-term storage, or refrigerated for short periods. [25], [21]
- After mixing. Once the powder is mixed with liquid (reconstituted), pages say to refrigerate it at 2–8 °C (36–46 °F), but their “use within” times range from 14 days to 30 days, and some simply say to follow the product's instructions. None cites a stability test. [14], [25], [47], [18], [7]
- Pens. The Ukrainian pen seller says to keep pens at 2–8 °C. [15]
- Suppositories. The 2017 patent says its suppositories are “stable on storage” but gives no shelf life for the public. [34]
Health Canada warns that unauthorized injectable peptides may not have been made or stored safely, and cold storage cannot tell you what is in a vial (see product quality). [55]
What do we actually know about Prostamax in people?
Very little. The only human data are three small patient series described in two patents: two from the developers in 2001 and one from a second company in 2017. None was published in a journal or described as randomized (assigned by chance) or blinded (hiding who got what), and none described how side effects were collected. ClinicalTrials.gov has no Prostamax study. [1], [34], [56]
Some evidence-review websites, and an earlier version of this guide, said there were no human data. The patent examples do exist and can be read; they are simply weak evidence. [49], [13]

What did the patent examples report?
| Report | What was reported | What it cannot establish |
|---|---|---|
| Chronic prostatitis, 2001 patent | 35 men aged 23–45 whose symptoms had not settled on usual treatment received 0.01–100 mcg per kg into a muscle once a day for 10–40 days; 14 similar men had usual treatment. Pain disappeared in 64.0% and eased in 32.7%. Frequent urination stopped troubling 87.5%. Sexual function recovered in 44.4% of those with problems and improved in 41.8%. Average urine flow rose from 17.3 to 23.5 mL per second. Blood counts and blood chemistry showed “no significant deviations”. | Whether Prostamax caused the change. The control group's results are not given, individual doses are not given, and several percentages cannot be whole numbers of 35 men. [1], [2] |
| Prostate adenoma (BPH), 2001 patent | 19 men aged 51–67 with stage I–II adenoma received the same range for 10–40 days; 17 similar men had usual treatment. Daytime urination fell from 8.4 to 6.3 times, average flow rose from 11.3 to 17.5 mL per second, and 37.3% reported better libido. | The same limits. Night-time urination barely changed (3.1 to 2.6 times). No symptom score such as the IPSS and no PSA were reported. [1], [2] |
| BPH suppositories, 2017 patent | 16 men aged 50–63 with stage I–II BPH used rectal suppositories once a day for 10–40 days; a comparison group of 5 similar men took other medicines. Questionnaires showed improvement; in 4 men on the highest dose and longest course, ultrasound showed the adenoma about 10–13% smaller; 52% reported better libido. | Anything about dose: the patent gives the amount per suppository as both 0.3–1.0 mg and 0.3–1.0 mcg. The comparison group's results are not given. [34] |

The only human data: three patent case series
- Chronic prostatitis · 2001 patent
- People: 35 men aged 23–45 treated; 14 on usual treatmentRoute: Into a muscle, 0.01–100 mcg/kg once daily, 10–40 daysPublished in a journal: ○ NoRandomized: − Not describedBlinded: − Not describedControl group results reported: ○ NoIndividual doses reported: ○ NoSide effects collected: − Not describedPSA measured: ○ No
- Prostate adenoma (BPH) · 2001 patent
- People: 19 men aged 51–67 treated; 17 on usual treatmentRoute: Into a muscle, same range, 10–40 daysPublished in a journal: ○ NoRandomized: − Not describedBlinded: − Not describedControl group results reported: ○ NoIndividual doses reported: ○ NoSide effects collected: − Not describedPSA measured: ○ No
- BPH suppositories · 2017 patent
- People: 16 men aged 50–63 treated; 5 on other medicinesRoute: Rectal, once daily, 10–40 days; dose printed as 0.3–1.0 mg and 0.3–1.0 mcgPublished in a journal: ○ NoRandomized: − Not describedBlinded: − Not describedControl group results reported: ○ NoDose clearly stated: ○ No (1,000-fold conflict)Side effects collected: − Not describedPSA measured: ○ No
Registered clinical trials of Prostamax: 0 (ClinicalTrials.gov, searched 24 Sep 2026)
70 treated men, all in patents: none published in a journal, none described as randomized or blinded, and no trial registered.
Why are these reports so hard to judge?
Patents are written to claim an invention, not to test it. In the 2001 examples, the men were already taking or had taken other treatments, the patent describes results only “before” and “after” in the treated men, and the 14 and 17 control patients appear only as a sentence. Symptoms like these vary over time, so a before-and-after change without a comparison group says little. [2]
The numbers also do not quite add up. For example, 64.0% of 35 men would be 22.4 men, and 37.3% of 19 would be 7.1. That suggests the percentages were worked out on different groups than described. None of this means the reports are false; it means they cannot be checked. [2]
Were there other studies in people?
Not with Prostamax given to people. Several papers used white blood cells from very old volunteers, but the cells were treated in the laboratory; the volunteers never received the peptide. [39], [57] A 2010 dissertation on prostate disease in older men tested Prostamax only on rat tissue in a dish. [58] The older clinical papers on prostate peptides describe Prostatilen, an animal extract, and cannot be counted for the lab-made peptide. [59], [60]
A 2012 paper often cited as Prostamax evidence in human prostate cells actually tested a different peptide, Vesugen (Lys-Glu-Asp). [61]
What do the urinary measures mean?
- Urine flow rate (uroflowmetry) measures how fast urine comes out, in mL per second. Weaker flow is typical of BPH, but a single test varies with how full the bladder is.
- Daytime and night-time urination are counts from the patient's own diary or recall.
- The IPSS (International Prostate Symptom Score) is a standard seven-question score doctors use for BPH symptoms. None of the Prostamax reports used it.
- Prostate size is measured by ultrasound. Only the suppository patent gives a number, for 4 men. [34]
What the reports did not measure is what matters most over years: symptom scores, PSA, urinary retention, the need for surgery and side effects.
How might Prostamax work?
The developers' idea is that short peptides act as tissue-specific signals that switch genes on or off in their target organ. For Prostamax, that means prostate cells. The experiments below test pieces of that idea. They are preclinical (in rats, tissue pieces, cells and test tubes), and nearly all come from the developer's network and its commercial partner.

Does it act only on the prostate?
Not in the developers' own experiments. At 0.05 ng per mL, Prostamax increased the growth of small pieces of rat prostate kept alive in a dish (explants) by about 25%, and fewer prostate cells stained for p53, a protein that can halt damaged cells. [62], [53] But in the same program it reduced the growth of pieces of deep brain tissue by 28% in young rats and 23% in old rats, and it stimulated skin tissue. [63], [53], [54] In the patent, it also increased the growth of bladder tissue from chick embryos by 23%. [2] So its effects in a dish are not limited to the prostate, and what a slower-growing brain explant means in a living body is unknown.
What happened in rats with prostatitis?
- Infection model (patent). Rats with prostatitis caused by E. coli bacteria received 0.1 mcg by subcutaneous injection daily for 10 days. The average inflammation score was 1.81 on Prostamax, 2.36 with salt water and 2.91 without treatment, but 7 of 11 rats still had prostatitis in both the Prostamax and salt-water groups. [2]
- Surgical model, 2013. In 60 rats with chronic prostatitis caused by surgery (without infection), 20 mcg per kg into a muscle for 15 days reduced scarring: the area of collagen fibers fell more than 2.5-fold and the gland's density returned to normal, similar to a prostate extract and a saw palmetto product. The operated glands had not grown larger in this model, so it could not test shrinkage. [37]
What happened in rats with an enlarged prostate?
In a 2014 study, 40 rats were given sulpiride, a drug that raises the hormone prolactin and more than doubled the size of the side lobes of their prostates. Adding the peptide into a muscle every day for 60 days made those lobes 24% lighter and 40% smaller in volume than in rats given sulpiride alone. The paper prints the dose as 20 mg per kg, a thousand times the 20 mcg per kg the same group used in 2013, and the discrepancy is unexplained. [38]
Does it affect male hormones?
Possibly, and in the opposite direction to the marketing. A 2011 conference abstract from the Tomsk team and Geropharm tested 20 and 40 mcg per kg in rats and mice. The seminal vesicles, glands that depend on male hormones, were 23.5–42.9% lighter relative to body weight, which the authors describe as an “anti-androgenic” effect (androgens are male hormones such as testosterone). The same abstract reports an 84% rise in urine output at 40 mcg per kg, less swelling in an inflammation test and 54–60% lower pain responses. [24]
This is one abstract without hormone blood tests, group sizes or a stated route, so it is a signal, not a finding. A 2010 dissertation also describes Prostamax as having anti-androgenic effects, without data. [58] It is not a steroid or a hormone itself.
Does it reduce inflammation?
In a blinded 2011 study in 90 rats funded by Geropharm, only the highest dose tested, 1,000 mcg per kg into the belly cavity, reduced paw swelling (by 23% at 2 hours and 19% at 4 hours). The standard anti-inflammatory drug diclofenac almost completely blocked it. [64]
What does it do to chromatin in white blood cells?
Chromatin is DNA wound around packaging proteins. In white blood cells from people aged 75–88, grown in the laboratory, Prostamax loosened tightly packed chromatin, which the developers treat as reversing an aging pattern. [39], [4] In a 2012 study in cells from people aged 75–86, it also doubled sister-chromatid exchanges from 5.9 to 12.0 per cell. [57] The authors read that as chromatin opening up. Toxicologists have long used a rise in these exchanges as a sign that a substance may damage DNA, so the finding needs a safety explanation that no study has provided. [65]
A 2009 paper sometimes cited for this effect reports results for copper and cadmium only in its abstract, not for Prostamax. [66]
Does it bind DNA?
That is the proposed mechanism, but it has been shown only in test tubes and computers. In a test tube, Prostamax and other short peptides changed the temperature at which DNA strands separate, and a computer model predicted a binding site on DNA. Neither shows the peptide reaching DNA inside a living prostate. [67], [68]
What are the risks and unanswered questions?
Is Prostamax safe?
Its safety in people has not been established. The chronic prostatitis example reports only that repeated blood counts and blood chemistry showed “no significant deviations”, with no description of how side effects were looked for, and the courses lasted 10–40 days. [2]
The patent's animal tests found no deaths or organ damage in mice given single doses of 1–5 mg per kg, in rats given up to 3 mg per kg daily for 90 days, or in rats given up to 1 mg per kg daily for six months, all into a muscle. No lethal dose was found. These were the inventors' own tests, reported briefly, and no long-term cancer study has been done. [1]
Could it hide prostate cancer or confuse a PSA test?
This is the most important practical risk. PSA is a protein made by normal and cancerous prostate cells. It can rise with prostate cancer, BPH or prostatitis, and temporarily after infection, a biopsy, vigorous cycling or ejaculation. [23] A raised PSA is a reason for medical assessment, not for a trial of a peptide.
No study has measured what Prostamax does to PSA, in either direction. [2], [56] Two things are known from other medicines: finasteride lowers PSA by about half, so doctors double the reading to interpret it, and a confirmed rise on finasteride still needs checking. [69] Any product that changed PSA without that kind of correction could make a reading harder to interpret.
In public forums and community education groups, people describe starting Prostamax to bring a raised PSA down, including one spouse who ordered it for her husband during an active urology workup. One public forum user's PSA rose while he took it and had fallen only to about 13 some six weeks after he stopped. [43] In one community education group, a member whose enlarged prostate turned out to be cancer urged others to get checked first.
Could it lower male-hormone activity?
Possibly. The only animal data on hormone-dependent organs found smaller seminal vesicles in rats, which the authors called anti-androgenic, and no study measured testosterone or other hormones. [24] Whether this happens in men, and whether it matters for sexual function, fertility or people on testosterone therapy, is unknown.
What problems have actually been reported?
Very few, and none formally. One public forum user reported “tremendous prostate pain” after using it, and another said he was “peeing all day” on his second day at about 1 mg a day. [43], [16] No one in the community education groups reviewed described side effects from Prostamax, but few reported any structured checks, so their silence says little about safety. No published case report of harm was found.
Could product quality change the risk?
Yes. Research vials are sold without the testing required for medicines, and in community education groups members reported that certificates of analysis were rare, that few labs test bioregulators and that one vial arrived without its vacuum seal. Pages disagree about the molecule, and at least two print the wrong sequence. [32], [40] Health Canada warns that unauthorized injectable peptides may cause infection or allergic reactions, may contain ingredients or contaminants not on the label and may not have been made or stored safely. [55]
When is it urgent?
Some urinary problems need prompt care whatever else you are taking. US health guidance says to tell a health professional right away if you cannot urinate at all; have painful, frequent and urgent urination with fever and chills; see blood in your urine; or have great discomfort or pain in your lower abdomen or urinary tract. [22]
Is Prostamax legal? Is it FDA-approved?
Checked September 24, 2026. Rules differ by country and change quickly. A “research use only” label does not make a product legal to sell or safe to use.
United States. Prostamax is not an FDA-approved medicine: a search of FDA's approved-drug database found no entry. [70] On June 17, 2026, FDA sent a warning letter to a US peptide seller stating that its “Prostamax” is an unapproved new drug under section 505(a) of the Federal Food, Drug, and Cosmetic Act, citing website claims about BPH and prostatitis. [9] It is not among the substances nominated for pharmacy compounding (list updated May 14, 2026), not on FDA's list of compounding substances that may pose significant safety risks, and not in the compounding regulation's list of allowed bulk substances. [71], [72], [73]
Canada. Health Canada's August 1, 2025 advisory names Prostamax among unauthorized injectable peptide drugs seized from a seller. It is the only Health Canada record for Prostamax, including archived records. Selling unauthorized drugs is illegal in Canada. [55], [74], [75]
Australia. Prostamax is not named in the June 2026 Poisons Standard, and the Therapeutic Goods Administration's (TGA's) 2026 warnings on unapproved peptides do not name it. A live search of the Australian Register of Therapeutic Goods could not be completed. The TGA says unapproved peptide products “have not been assessed by the TGA for safety, quality or effectiveness”, and personal importation is permitted only if products are clearly and accurately labelled; labelling is one condition, so a well-labelled vial is not automatically legal to import. [76], [77], [78]
United Kingdom. A search of UK government sites, which include the medicines regulator (MHRA), found no record for Prostamax. [79]
Russia and elsewhere. We found no Russian medicine registration or supplement certificate for the lab-made peptide, but the Russian registers could not be searched. The medicine registered as Prostamax in Uzbekistan is a prostate-extract suppository, not KEDP. [6], [10]
Is Prostamax banned in sport? Does it show up on a drug test?
Prostamax is not named on the World Anti-Doping Agency's 2026 list or on the 2027 list that takes effect on January 1, 2027. Category S0 bans at all times any substance “with no current approval by any governmental regulatory health authority for human therapeutic use”, and the 2027 list adds “peptides” to its examples. WADA has not ruled on Prostamax specifically, so tested athletes should assume S0 can apply. [80], [81] No published anti-doping test for Prostamax was found.
Who should be especially cautious?
These groups have no safety data. That is a reason for caution, not proof of harm.
- Anyone with a raised or rising PSA, blood in the urine, or a prostate being investigated. Assessment comes first (see above). [23], [22]
- Anyone taking prescribed prostate medicines such as alpha blockers, finasteride or dutasteride, or tadalafil. In community education groups, two members stopped their alpha blocker during a self-directed course. Changes belong with the prescriber. [22]
- Anyone awaiting prostate surgery or other planned treatment. In one community education group, a member described a friend using it while waiting for surgery; no study has looked at it before or after surgery.
- Men on testosterone therapy or trying to conceive, because of the rat anti-androgenic signal and the lack of hormone data. [24]
- Young men with pelvic pain. Chronic pelvic pain has several causes, and in community education groups it has been suggested even for men in their early 20s. Prostamax has not been studied in young men beyond the patent example. [36]
- Children and teenagers, and anyone who is pregnant or breastfeeding. Never studied; this guide is written for adults.
- Competitive athletes. See the anti-doping section above. [80]
Has Prostamax been tested alongside other medicines?
No. The men in the patent examples had previously used other treatments, which the patent does not list. Nothing is known about combining Prostamax with alpha blockers such as tamsulosin, 5-alpha reductase inhibitors such as finasteride, tadalafil, testosterone, GLP-1 weight-loss medicines or other peptides. [2]
In public forum and community education group reports, it was often combined with a bladder bioregulator, tadalafil, weight loss or testosterone, which makes it impossible to say which one helped. [82], [16] Bring a complete list of everything you take to a pharmacist or doctor.
What should be monitored while using Prostamax?
No regulator has written a monitoring plan for Prostamax, and the vials are sold for laboratory research with no approved label. What exists is a record of what the patent examples measured and general guidance on prostate symptoms. It can help you prepare questions for a clinician; it is not a personal testing plan. [2]
What did the patent examples check?
- Urination: flow rate on uroflowmetry, time to maximum flow, daytime and night-time counts, and 5-point scores for straining and stream strength. [2]
- The prostate: examination by finger, prostate secretions in the laboratory and ultrasound. [2]
- Safety blood tests (chronic prostatitis example): full blood count, clotting tests, blood chemistry and urine tests before and after the course. [2]
- Sexual function and libido: by patient report. [2]
They did not report PSA, symptom scores such as the IPSS, hormone levels or side effects.
Which measures matter, and why?
| Why it matters | What studies measured or guidance says | Tracking category |
|---|---|---|
| Whether urinary symptoms change | Flow rate, daytime and night-time urination counts, straining and stream scores [2] | Other (urinary symptoms); Sleep (night-time waking) |
| Ruling out cancer and infection | PSA was not measured in any Prostamax report; it can rise with cancer, BPH or prostatitis, and several things raise it temporarily [23] | Other (PSA) |
| Hormone effects | Seminal vesicles shrank in rats; no hormone tests in any study [24] | Hormonal & Reproductive; Sexual Health |
| General safety | Blood counts, chemistry and urine tests in the chronic prostatitis example [2] | Tolerability |
| Pain in chronic prostatitis | Pain disappearance or easing by patient report [2] | Pain & Inflammation |
| Injection problems | Health Canada warns of infection and allergic reactions with unauthorized injectable peptides [55] | Tolerability |
In community education groups, the more careful educators insist on a PSA baseline (total, free and percent free) before a course, a repeat test 4–6 weeks after it, and stopping after two courses that change nothing. That is educator advice, not a tested plan. Because ejaculation, cycling, infection and a recent biopsy can raise PSA temporarily, tests are usually timed to avoid them. [23]
Health Canada advises anyone who has used an unauthorized injectable drug and has health concerns to consult a health care professional, and to report side effects. [55]
What do people in public communities report?
Public accounts are few, and all the readable first-hand ones are on Reddit. Most describe urinary symptoms, and almost none include a diagnosis, lab results or measured flow. [16], [17], [42], [43]
What do the positive reports look like?
- A user with long-standing dribbling and self-described prostatitis took 750 mcg a day by subcutaneous injection for 3 weeks and described a much better stream, with the effect lasting about six months, after which he started a prostate supplement. [16]
- Another took 750 mcg each morning for three weeks without any tests and went from four night-time trips to one, while also taping his mouth at night and drinking less overnight. [17]
- A man with BPH described less pain and one or no night-time trips after combining Prostamax with a bladder bioregulator. [82]
- The poster of one thread took 5 mg a day by subcutaneous injection and reported a wider stream within about five days; later in the thread he said the gland had not really shrunk but felt less tender. [43]
In community education groups, reports of benefit were also about flow, emptying, urgency and night-time trips, appearing from about one to five weeks into a course. About half of those accounts involved something else at the same time: a bladder bioregulator, tadalafil, large weight loss on GLP-1 medicines or testosterone therapy. Members' own summaries were modest, describing relief rather than a cure.
Does everyone notice a difference?
No. One user with BPH had no benefit from two months of injections and none from Libidon afterwards, and another in a second thread noticed nothing at 1 mg a day. [42], [43] In community education groups, one man felt no effect from a full course and credited his later improvement to losing weight, correcting his hormones and exercising; another took 2 mg a day for about three months with little change and no change on examination. Educators in one group say that no noticeable change is the most likely outcome for this class of peptides.
Someone who said he was starting a course and would report back never posted again, a common pattern that leaves outcomes unknown. [83]
What about unwanted effects?
Two public reports: severe prostate pain in one user and heavy urination on day two in another, both brief and without follow-up. See the risks. [43], [16] The more worrying pattern is not a side effect but a decision: using Prostamax to bring down a raised PSA, or stopping a prescribed medicine, instead of getting checked.
What do community education groups teach?
Educators disagree more than they agree. One group describes Prostamax as the only prostate bioregulator and as made from prostate tissue; in fact it is lab-made, and several prostate extract products exist. Another lists it as a way to act on DHT (a potent male hormone) without androgenic side effects, which the rat data do not support. Claims that it relaxes the muscles of the urinary tract or lowers PSA have no study behind them. More careful lessons stress that the research comes from one institute, that extract and lab-made products are often confused, and that a PSA baseline and a stop rule are essential. [1], [24]
Some lessons reuse seller text or carry purchase links, so enthusiastic lessons are not independent evidence.
How can you judge a prostate story?
Ask: Was there a diagnosis, and was PSA checked before and after? What else changed: a new or stopped medicine, tadalafil, weight loss, evening drinking, testosterone? Was flow or night-time urination counted the same way before and after? Which product, how much and by which route? What happened months later?
These selected discussions are not a survey of all users, a response rate or a substitute for controlled studies. Symptoms vary from week to week, and people are more likely to post when something seems to work.
How does Prostamax compare with Pancragen, Crystagen and Epitalon?
Prostamax belongs to a family of very short peptides from the same Russian program, and some share most of its chain. Pancragen has the same first three amino acids (Lys-Glu-Asp) with a different fourth, and Crystagen is Prostamax's last three (Glu-Asp-Pro). Epitalon is the best-known member of the family. The table compares what each one is and how much has been tested in people.
| Compound | What it is | How it is taken | How often | Human evidence | Approval status |
|---|---|---|---|---|---|
| Prostamax (this guide) | Four amino acids (Lys-Glu-Asp-Pro, KEDP), promoted for the prostate [1] | Injection: into a muscle in the patent, mostly subcutaneous in practice [1], [14] | Websites: once daily for 10–20 days, or 8–12 weeks stepping up [14], [19] | Patent case series (54 men) plus a second patent (16 men); none published in a journal [1], [34] | Not approved; FDA called one seller's product an unapproved new drug in 2026 [9] |
| Pancragen | Four amino acids (Lys-Glu-Asp-Trp) from the same program, promoted for the pancreas [84] | Capsules by mouth; vials by subcutaneous injection, according to protocol websites [85], [86] | Capsules 1–2 times a day for a month, repeated after 4–6 months [85] | Four small reports from the developer's network, one with a placebo [84], [87] | Supplement in Russia; not an approved medicine [85], [88] |
| Crystagen | Three amino acids (Glu-Asp-Pro) from the same program, promoted for the thymus [89] | Capsules by mouth; vials by subcutaneous injection, according to protocol websites [90], [91] | Capsules 1–2 times a day for a month, repeated after 3–6 months [90] | Two small reports on immune blood tests without a placebo [89], [92] | Supplement in Russia; not an approved medicine [90], [93] |
| Epitalon | Four amino acids (Ala-Glu-Asp-Gly) made in a lab, modeled on a pineal extract [94] | Websites: subcutaneous injection; studies: into a muscle and other routes [95], [96] | Websites: 5 mg once daily for 20 days, then 4–6 months off [95] | A few small studies from the same network, measuring melatonin and vision [96], [97] | Not approved; FDA advisers voted 7 to 4 in July 2026 to add it to the pharmacy compounding list; FDA has not decided [98] |
The real differences are small. All four come from one research network, all rest on small reports without independent repetition, and none has a registered trial with results. Pancragen and Crystagen at least have registered capsule products with stated amounts; Prostamax does not. No study has compared Prostamax with any of them, or with the approved BPH medicines, in people. Prostatilen, Libidon and Vitaprost, which people often mention alongside Prostamax, are animal prostate extracts with no Doserly guide (see the common questions).
Common questions about Prostamax
Is Prostamax the same as Prostatilen, Libidon or Vitaprost?
No. Prostamax is a single lab-made peptide (Lys-Glu-Asp-Pro). Prostatilen is a preparation extracted from animal prostate tissue, which the Prostamax patent names as the product it was designed to replace; Libidon capsules contain a natural prostate “peptide complex”. Research and reviews of those extracts cannot be counted for Prostamax, and a medicine sold as Prostamax in Uzbekistan is itself a prostate extract. [2], [12], [41], [10] See what Prostamax is.
Can Prostamax shrink an enlarged prostate?
It has not been shown in people. One rat study with an unexplained dose found smaller drug-enlarged glands, and the suppository patent reports about 10–13% smaller adenomas in 4 men without a proper comparison. In a public forum, one man taking 5 mg a day said his gland “hasn't really shrunk”. By contrast, US health guidance describes 5-alpha reductase inhibitors, an approved medicine type, as helping stop the growth of or shrink the prostate. [38], [34], [43], [22] See how it might work.
Does Prostamax lower PSA?
No study has measured it. Neither patent reports PSA, and no trial exists. If PSA is raised, the cause needs to be found first: it can come from BPH, prostatitis or cancer, and a lower number on any product does not rule out cancer. [2], [23] See the PSA risk.
Does Prostamax raise testosterone? Is it a steroid?
It is not a steroid or a hormone; it is a four-amino-acid peptide. No study measured testosterone. The only related animal data point the other way: in a rat abstract, seminal vesicles shrank, which the authors called an anti-androgenic effect. [3], [24] See the hormone question.
Is Prostamax a pill or an injection?
In practice, an injection. It is sold as vials of powder to mix with sterile water or as prefilled pens. Capsule doses printed online could not be traced to any product, and a suppository exists only in a patent. [7], [15], [8], [34] See the protocol tables.
How long does Prostamax take to work?
There is no reliable answer. The patent examples measured results after 10–40 days. Public forum users describe changes from about five days to three weeks, and community education group members from about one to five weeks, often while doing other things at the same time. [2], [43], [16] See what people report.
Can Prostamax replace tamsulosin, finasteride or tadalafil?
The reviewed evidence gives no reason to think so. Those medicines are approved treatments for BPH; Prostamax has only patent case series and has never been compared with them. Any change to a prescribed medicine should be agreed with the prescriber. [22], [35], [2] See who should be cautious.
Is it legal to buy Prostamax?
It depends on the country. It is not approved as a medicine in the United States, where FDA has called one seller's Prostamax an unapproved new drug, and Health Canada lists it among seized unauthorized injectable peptides. A “research use only” label does not make a product legal or safe. [9], [55] See the dated legal-status summary.
Glossary
Plain explanations of the route, dosing and research terms used in this guide. Underlined terms in the text link here.
- Adverse event
- A harmful or unwanted medical event reported after someone used a treatment. A report alone does not prove the treatment caused it.
- Alpha blocker
- A type of prescription medicine, such as tamsulosin, that relaxes the muscles of the bladder neck and prostate so urine flows more easily. It is a standard treatment for BPH.
- Amino acid
- A small chemical building block. Chains of amino acids make up peptides and proteins.
- Androgen (anti-androgenic)
- Androgens are male hormones such as testosterone and DHT. An anti-androgenic effect is one that lowers their activity, for example by shrinking organs that depend on them.
- Animal study
- Research in animals such as rats or mice. It shows what a substance does in a living body, but results in people can differ.
- Bioavailability
- How much of a dose reaches the bloodstream in a usable form. It depends heavily on the route. For Prostamax it has not been measured by any route.
- Bioregulator
- The name a Russian research group uses for very short peptides it believes act on particular tissues. It is a marketing and research label, not a regulatory category.
- Blinded
- A study design in which participants, and often researchers, do not know who got the treatment and who got the comparison, so expectations cannot sway the results. None of the Prostamax reports describes blinding in people.
- BPH (benign prostatic hyperplasia)
- Growth of the prostate that is not caused by cancer. It is common with age and can weaken the urine stream and cause frequent or night-time urination. Older papers call it prostate adenoma.
- Cell study (in vitro)
- Research on cells grown in a dish. It gives early clues about biology, but it is far from proof of benefit in people.
- Chromatin
- DNA wound around packaging proteins inside the cell nucleus. Tightly packed chromatin keeps genes switched off; loosened chromatin lets them be read.
- Compounding
- A pharmacy making a medicine for an individual patient from raw ingredients. In the US, pharmacies may only compound with bulk ingredients on FDA's allowed lists; Prostamax is not on them.
- Controlled trial
- A study that compares people who receive a treatment with a similar group who do not, often receiving a placebo instead. Randomly assigning people to each group makes the comparison fairer.
- Course and cycle
- A course is the period of repeated use, such as 10 days. A cycle is a course plus a planned break before any further use.
- Daily total
- All the amounts given in one day, added together. For example, 5 mg twice daily is a 10 mg daily total.
- Dose (amount each time)
- The amount given on one occasion. A protocol lists both the dose and how often it is given.
- Explant
- A small piece of tissue kept alive in a dish. Researchers measure how far cells grow out from its edge to compare treatments.
- 5-alpha reductase inhibitor
- A type of prescription medicine, such as finasteride or dutasteride, that blocks the conversion of testosterone to DHT and can shrink an enlarged prostate. It lowers PSA by about half.
- Half-life
- The time it takes for the measured level of a substance in the blood to fall by half. It is not the same as how long an effect lasts. Prostamax's has not been measured.
- Intramuscular (IM)
- Injected into a muscle. The patent's patients received Prostamax this way.
- Investigational
- Still being studied and not approved by a regulator, such as the FDA, to treat any condition.
- Freeze-dried (lyophilized)
- Dried by freezing and removing the water, leaving a powder. Prostamax vials are sold this way and mixed with liquid before injection.
- mcg and mg
- Micrograms and milligrams. 1 mg equals 1,000 mcg. Prostamax protocols use both, so check which one a page means.
- Oral
- Taken by mouth, as a capsule, tablet or liquid.
- Peptide
- A short chain of amino acids. Prostamax is a chain of four, called a tetrapeptide.
- Pharmacokinetics
- How the body absorbs, moves, breaks down and removes a substance. For Prostamax, no data exist in any species.
- Placebo
- A dummy treatment with no active ingredient, used as a comparison in studies. No Prostamax study used one.
- Preclinical research
- Studies done before research in people: cell studies, tissue cultures, test-tube experiments and animal studies.
- Prostatitis
- Inflammation of the prostate. It includes chronic prostatitis or chronic pelvic pain syndrome, bacterial infections and inflammation found without symptoms.
- PSA (prostate-specific antigen)
- A protein made by prostate cells and measured in a blood test. It can rise with prostate cancer, BPH or prostatitis, and briefly after ejaculation, cycling or a biopsy.
- Reconstitution
- Mixing a freeze-dried powder with a liquid so it can be measured and injected. The amount of liquid sets how much peptide each unit holds.
- Rectal
- Given into the rectum, for example as a suppository that melts at body temperature.
- Research use only
- A label on products sold for laboratory research. It does not mean a product is approved, tested for human use or legal to sell as a medicine.
- Sister-chromatid exchange
- A swap of DNA between the two copies of a chromosome made when a cell divides. Toxicologists have used a rise in these swaps as a sign that a substance may damage DNA.
- Seminal vesicles
- Two small glands behind the bladder that make most of the fluid in semen. Their size depends on male hormones, so researchers weigh them to judge hormone activity in rats.
- Subcutaneous (SC)
- Injected into the fatty layer just under the skin. This is the route most people who use Prostamax describe.
- Syringe units
- Markings on an insulin syringe that measure volume. On a U-100 syringe, 100 units equal 1 mL. The amount of drug per unit depends on the vial's concentration.
- Titration
- Adjusting a dose in steps, usually starting lower and increasing if needed.
- Uroflowmetry
- A test that measures how fast urine flows, in millilitres per second, while a person urinates into a special device.
- WADA
- The World Anti-Doping Agency, which publishes the list of substances banned in sport.
Explore more of the research
Go deeper into the experiments behind the claims.
Across this guide, the citations include 12 original scientific papers on Prostamax: two rat studies, six cell and tissue-culture studies, one test-tube chemistry study and three computer-modelling papers. None reports a study in people. The two patent families, two conference abstracts and three dissertation summaries are counted separately. Paper counts are not counts of independent research teams: nearly all come from one research network and its commercial partner.
Rats and mice · 2 papers, 2 abstracts, 2 patents
What do the patent's animal experiments claim?
Model: Mice and rats given the peptide into a muscle for toxicity; rats with E. coli prostatitis given 0.1 mcg by subcutaneous injection for 10 days; 18 rats aged 24 months given 0.1 mcg for 10 days.
Finding: No deaths or pathology at single doses up to 5 mg/kg in mice, or daily doses up to 3 mg/kg for 90 days and 1 mg/kg for 6 months in rats; average prostatitis score 1.81 versus 2.36 with salt water; in old rats, a marker of fat oxidation fell in the liver and an antioxidant enzyme rose in the brain.
Limit: Inventor data in a patent, briefly reported; 7 of 11 rats still had prostatitis in both the treated and salt-water groups.
Does it reduce scarring in surgical prostatitis?
Model: 60 rats with chronic prostatitis caused by surgery; 20 mcg/kg into a muscle for 15 days, compared with a prostate extract and a saw palmetto product.
Finding: Collagen area fell more than 2.5-fold and gland density returned to normal, similar to the comparison products.
Limit: The model did not enlarge the gland; the abstract's claim of more sexual activity has no data in the paper.
Does it shrink a drug-enlarged prostate?
Model: 40 rats given sulpiride for 60 days, with or without the peptide into a muscle daily.
Finding: Side-lobe mass 24% lower and volume 40% lower than with sulpiride alone; less gland lining under the microscope.
Limit: Dose printed as 20 mg/kg, a thousand times the group's 2013 dose; inconsistent wording about the saw palmetto group.
Does it change hormones, pain and urine output?
Model: Rats and mice at 20 and 40 mcg/kg.
Finding: Less carrageenan swelling, 54–60% lower pain responses, seminal-vesicle weights 23.5–42.9% lower, urine output up 84%.
Limit: Conference abstract only; no hormone tests, route or group sizes.
Does it reduce paw swelling?
Model: 90 rats, blinded, 10–1,000 mcg/kg into the belly cavity before an agar injection.
Finding: Only 1,000 mcg/kg reduced swelling (23% at 2 hours, 19% at 4 hours); diclofenac almost fully blocked it.
Limit: Conference abstract; funded by Geropharm.
What did the suppository patent test in animals?
Model: 60 rabbits given a single rectal dose of 5 mg/kg; rabbits with enlarged prostates.
Finding: No deaths; the chosen formulations were described as the most effective.
Limit: Company patent; its examples mix up rats and rabbits.
Tissue pieces in a dish · 2 papers, 3 dissertations
Does it make prostate tissue grow?
Model: Small pieces of prostate from young and old rats kept alive in a dish, with 0.05 ng/mL of peptide.
Finding: Growth of prostate pieces increased compared with untreated pieces.
Limit: Tissue growth in a dish is not prostate repair in a living animal.
Is the effect specific to the prostate?
Model: Rat tissue pieces from several organs treated with each of six short peptides.
Finding: Prostamax raised prostate growth by 25 ± 4% and lowered p53 staining in prostate tissue (0.19 versus 0.73), but lowered the growth of deep brain tissue by about 28%.
Limit: Developer-group paper; fewer p53-positive cells is not automatically healthy.
What happened to brain and skin tissue?
Model: Rat brain and skin tissue pieces from young and old animals.
Finding: Brain tissue growth fell by 28 ± 5% (young) and 23 ± 3% (old); skin tissue was stimulated, including from old rats.
Limit: Dissertation summaries; not peer-reviewed papers.
Why was it studied for hormones?
Model: Rat prostate tissue pieces in a doctoral dissertation on prostate disease in older men.
Finding: Prostamax stimulated prostate tissue; the author says it was chosen for its anti-androgenic effects.
Limit: No data for the anti-androgenic statement; the patients in the dissertation did not receive Prostamax.
Does it make bladder tissue grow?
Model: Bladder pieces from chick embryos.
Finding: Growth increased by 23% at 20 ng/mL.
Limit: Bird embryo tissue in a patent example.
White blood cells, DNA and computer models · 4 cell papers, 1 test-tube study, 3 modelling papers
Does it loosen chromatin in old people's cells?
Model: White blood cells from people aged 75–88 grown in the laboratory with several short peptides.
Finding: Prostamax loosened tightly packed chromatin near the center of chromosome 1.
Limit: Abstract only; the donors did not receive the peptide.
Does it change chromatin melting?
Model: Human white blood cells in the laboratory; heat measurements of chromatin.
Finding: Melting peaks shifted by 2.9 °C and 1.0 °C; the paper names the free acid form.
Limit: Abstract only.
What happened to chromosome exchanges?
Model: White blood cells from 5 people aged 75–86, cultured with 0.01 mcg/mL.
Finding: Sister-chromatid exchanges doubled (5.9 to 12.0 per cell) and active ribosome-gene regions rose (0.95 to 2.5).
Limit: The authors did not examine whether the rise signals DNA damage.
Did copper and cadmium experiments test Prostamax?
Model: Human white blood cells with metals and Prostamax.
Finding: The abstract reports metal effects only.
Limit: No Prostamax result is stated.
Does it change DNA in a test tube?
Model: DNA melting with short peptides.
Finding: KEDP changed the temperature at which DNA strands separate.
Limit: Test tube only.
What do computer models predict?
Model: Docking of short peptides to DNA and to transporter proteins.
Finding: A predicted DNA binding sequence (“attc”); likely fits for LAT1, LAT2 and PEPT1 transporters in one paper, weak LAT1 binding in another.
Limit: Predictions; nothing was measured.
How this guide was researched
This guide is built from a thorough review of the sources cited throughout it: published scientific studies, patents, conference abstracts, dissertation summaries, trial-registry searches, regulatory documents, product registers, official labels and published protocol descriptions. We also reviewed public online forums and community education groups where people describe their own experiences with Prostamax.
The guide cites 98 sources, including 16 original scientific papers. Each type of source answers a different question. Studies show what researchers measured. Protocol descriptions show how Prostamax is typically used. Personal accounts show what individual people experienced. Every numbered citation links to its entry below, labeled by source type.
How this guide was made
Research and drafting were AI-assisted. Every cited source was checked against the original, and the guide was reviewed and edited by Doserly before publication. It has not had an independent clinical review, and Doserly does not currently have medical reviewers. Doserly makes a medication and health-tracking app and runs Doserly Academy, both of which are promoted in this guide. Read our editorial policy for how guides are researched, updated and corrected.
This guide is for educational purposes. It summarizes what the reviewed sources report so the research is easier to understand; it is not medical advice. For a deeper dive, or to check any point for yourself, go straight to the cited sources.
Explore the sources
These are the documents cited in this guide. Studies, patents, product pages, website advice and personal accounts answer different questions. A source being listed does not mean every statement on its page is endorsed.
Showing 98 sources
- 01
Тетрапептид, регулирующий функции предстательной железы, фармакологическое средство на его основе и способ его применения (Tetrapeptide regulating prostate functions, a pharmaceutical based on it and its method of use; RU2177802C1) ↗
Patent (human examples and animal data)
Full text reviewed (Russian original).
Result detail: Claims Lys-Glu-Asp-Pro and its salts by injection at 0.01–100 mcg per kg at least once daily for 10–40 days. Example 6: 35 men aged 23–45 with chronic prostatitis given the peptide into a muscle, with 14 conventionally treated men as controls. Example 7: 19 men aged 51–67 with stage I–II prostate adenoma (BPH), with 17 controls. Control results and individual doses are not reported, and no side-effect collection is described. Animal data: mice (single doses of 1–5 mg/kg, 78 mice) and rats (up to 3 mg/kg daily for 90 days, 48 rats; up to 1 mg/kg daily for 6 months, 56 rats) with no deaths or pathology reported; E. coli prostatitis in rats (0.1 mcg by subcutaneous injection daily for 10 days). Inventor data, not peer reviewed.
- 02
Tetrapeptide regulating prostate functions and its compositions and uses (EP1353939B1; same family as RU2177802 and WO2002066497) ↗
Patent (English text of the same examples)
Full text reviewed; used for English wording of Examples 6 and 7.
Limitation: Several percentages in Example 6 cannot be whole numbers of the 35 men (for example 64.0% of 35 is 22.4 people), and the English claims print one unit as “pg/kg”, a typo for mcg/kg.
- 03
PubChem Compound Summary for CID 9848296, Prostamax ↗
Chemical database
Record reviewed: H-Lys-Glu-Asp-Pro-OH (free acid), formula C20H33N5O9, molecular weight 487.5 g/mol.
- 04
[The influence of the peptide bioregulator prostamax on heterochromatin of human lymphocytes in situ] ↗
Cell study
Original abstract reviewed (English version of the journal abstract): names Prostamax as H-Lys-Glu-Asp-Pro-OH; the peptide shifted chromatin melting peaks in human white blood cells in the laboratory by 2.9 °C and 1.0 °C.
- 05
IV Российский симпозиум «Белки и пептиды»: новые разработки (IV Russian Symposium “Proteins and Peptides”: new developments) ↗
Company statement
Page reviewed (Russian): Geropharm and the Tomsk Institute of Pharmacology presented Prostamax as a new peptide drug “in joint development”.
- 06
Группа компаний «ГЕРОФАРМ»: общая презентация 2015 (Geropharm group: company presentation 2015) ↗
Company statement
Presentation reviewed (Russian): its product pipeline lists “Простамакс – Урология” (Prostamax, urology) as an original product in development; the development stage is not stated. No later registration was found.
- 07
Prostamax 20mg Vial Dosage Protocol ↗
Protocol source
Page checked 24 Sep 2026: 500 mcg a day in weeks 1–2, 750 mcg in weeks 3–4 and 1 mg from week 5, from a 20 mg vial mixed with 2 mL (750 mcg = 7.5 units); calls the route subcutaneous in its introduction and intramuscular in its chart; mixed vials refrigerated at 2–8 °C. A “5–10 mg for 5–10 days” line seen in March 2026 is no longer on the page.
- 08
Цитогены: пептиды Хавинсона (Cytogens: Khavinson peptides; institute product catalogue) ↗
Developer catalogue
Page reviewed (Russian): the current catalogue of lab-made peptide capsules does not include Prostamax.
- 09
Warning Letter: Wholesale Peptide (MARCS-CMS 729447) ↗
Regulator
Letter reviewed: FDA states that the seller’s “Prostamax” and “Gonadorelin” are unapproved new drugs under section 505(a), quoting website claims about BPH, prostatitis and bladder control.
- 10
Простамакс суппозитории ректальные 50 мг (Prostamax rectal suppositories 50 mg): medicine certificate record ↗
Medicine register (different product)
Record reviewed (Russian): a registered medicine sold under the trade name Prostamax whose nonproprietary name is “prostate extract”, made by AO Cytomed (Russia) and classed as a BPH medicine. It is not the lab-made Lys-Glu-Asp-Pro peptide.
- 11
Простамакс капсули (Prostamax capsules, Ukraine): pharmacy directory entry ↗
Product listing (different product)
The page blocked direct access when rechecked; its saw palmetto (Serenoa repens) content was recorded by two separate research passes and in an earlier version of this guide, so it is cited only to explain the name confusion.
- 12
Цитомаксы: пептиды Хавинсона (Cytomaxes: Khavinson peptides; natural extract catalogue, including Libidon) ↗
Developer catalogue
Page reviewed (Russian): Libidon is listed as a natural peptide complex from prostate tissue sold as a dietary supplement, not the lab-made Prostamax peptide.
- 13
Prostamax: Research Evidence & Safety Profile ↗
Protocol source
Page checked 24 Sep 2026; source of the low subcutaneous row: “Anecdotal protocols commonly suggest subcutaneous injection of 100-200 ug daily for 10-20 days”, repeated every 3–6 months, “not validated”. Its claim of 200 mcg oral capsules has no traceable product, and it says there is no human use, missing the patent examples.
- 14
Prostamax: Research Overview & Mechanism ↗
Protocol source
Page checked 24 Sep 2026; source of the mid subcutaneous row: 0.75 mg once daily for 10–20 days by subcutaneous injection; also lists 0.5–1 mg daily; mixed vial refrigerated at 2–8 °C and used within 14 days.
- 15
Prostamax: Khavinson peptide for prostate (injection pen) ↗
Protocol source
Page checked 24 Sep 2026; source of the high subcutaneous row: the pen maker’s protocol of 20 clicks (2 mg) once daily by subcutaneous injection, 1 click = 100 mcg, one 20 mg pen for a 10-day course, 2–3 courses a year with 4–6-month breaks; stored at 2–8 °C.
- 16
Peptide for enlarged prostate? ↗
Community accounts
Thread read in full: one user describes 750 mcg a day by subcutaneous injection for 3 weeks with less dribbling and effects lasting about 6 months while later taking a prostate supplement; another improved with Prostamax plus tadalafil but trickling returned; another reports “peeing all day” on day 2 at about 1,000 mcg a day.
- 17
Peptide Prostamax ↗
Community account
Thread read in full: 750 mcg each morning for three weeks with a steadier stream and fewer night-time trips, while also taping the mouth at night and drinking less overnight; no diagnosis or tests.
- 18
Prostamax: Research Profile & Guide ↗
Protocol source
Page checked 24 Sep 2026; source of the short intramuscular row: 500 mcg to 1 mg into a muscle daily for 10–20 days, starting at 500 mcg and increasing to 1 mg “based on tolerance”, 3–6 months between cycles, 2–4 cycles a year; mixed solution used within 14–30 days. Its oral line (“10–20 mg orally once or twice daily”) has no traceable product.
- 19
Prostamax ↗
Protocol source
Page checked 24 Sep 2026; source of the stepped intramuscular row: 500 mcg once daily in weeks 1–2, 750 mcg in weeks 3–4, 1 mg in weeks 5–8 and beyond, over 8–12 weeks. Describes the free acid (H-Lys-Glu-Asp-Pro-OH).
- 20
Prostamax ↗
Protocol source
Page checked 24 Sep 2026: its summary card gives 500 mcg–1 mg a day, while its FAQ says “roughly 500 mcg to 20 mg per day, most often cited around 10-20 mg daily” for 10–20 days.
- 21
Prostamax 20mg Dosage Chart & Cycle Guide ↗
Protocol source
Page checked 24 Sep 2026: subcutaneous, 500 mcg rising every two weeks to 1,000, 2,000 and then 3,000 mcg once daily in weeks 7–12; 20 mg vial with 3 mL; powder at −20 °C, mixed vial refrigerated and not frozen.
- 22
Enlarged Prostate (Benign Prostatic Hyperplasia) ↗
Health information (government)
Page reviewed: symptoms, complications such as urinary retention, when to seek care right away, and medicine types (alpha blockers, 5-alpha reductase inhibitors and phosphodiesterase-5 inhibitors).
- 23
Prostate-Specific Antigen (PSA) Test ↗
Health information (government)
Page reviewed: PSA can rise with prostate cancer, BPH or prostatitis; infection, biopsy, vigorous exercise such as cycling and ejaculation can raise it temporarily; finasteride and dutasteride lower it.
- 24
Специфическая фармакологическая активность простатотропного пептидного препарата «Простамакс» (Specific pharmacological activity of the prostate-targeting peptide drug Prostamax) ↗
Animal study (conference abstract)
Full abstract reviewed (Russian).
Result detail: Rats and mice at 20 and 40 mcg/kg: less swelling in a carrageenan test at 20 mcg/kg; pain responses reduced by 54–60% in a writhing test; seminal-vesicle weight coefficients reduced by 23.5–42.9% (strongest at 20 mcg/kg), which the authors call anti-androgenic; urine output up 84% at 40 mcg/kg. Limitation: Abstract only; no hormone levels measured; route and group sizes not stated; a Geropharm employee is a co-author.
- 25
Prostamax 20mg Vial Dosage Protocol ↗
Protocol source
Page checked 24 Sep 2026: the same 500 → 750 → 1,000 mcg steps by injection into a muscle; powder refrigerated or frozen at −20 °C; mixed vial refrigerated and used within 2 weeks.
- 26
Prostamax ↗
Protocol source
Page checked 24 Sep 2026: lists 500, 750 and 1,000 mcg levels from the same template without week assignments.
- 27
Prostamax ↗
Protocol source
Page checked 24 Sep 2026: copies the 500 → 750 → 1,000 mcg steps to week 12 while also describing 10–20-day cycles.
- 28
Prostamax ↗
Protocol source
Page checked 24 Sep 2026: 20–40 mg a day by mouth, 1–2 times daily with food, for 10–30 days, 1–2 times a year; no product or source given for the capsule.
- 29
Prostamax ↗
Protocol source
Page checked 24 Sep 2026: oral capsules, 10–20 mg daily for 10–20 days; prints a molecular weight (473 Da) that does not match the peptide’s 487.5.
- 30
Prostamax ↗
Protocol source
Page checked 24 Sep 2026: “typical protocol 5–10 mg daily for 10 days”, with no source for the amount.
- 31
Prostamax Dosage Protocol: Reconstitution & Titration Guide ↗
Protocol source
Page checked 24 Sep 2026: 1–5 mg a day for a 10-day course, then months off; mixed vial used within 28 days. Cites PubMed 21267487 as a Prostamax paper; that record is an unrelated study of telomerase in HeLa cells.
- 32
Prostamax Dosing Protocol: 20 mg Vial ↗
Protocol source
Page checked 24 Sep 2026: 200 mcg daily for 10 days, 4–6 months between courses; prints the sequence as Lys-Asp-Glu-Leu, which is not Prostamax, and gives three different water volumes.
- 33
Prostamax ↗
Evidence summary website
Page checked 24 Sep 2026: presents the 2013 rat dose (20 mcg/kg into a muscle) in its dosing summary; that is an animal dose, not a human protocol.
- 34
Фармацевтическая композиция для лечения заболеваний предстательной железы в виде ректального суппозитория (Pharmaceutical composition for prostate diseases in the form of a rectal suppository; RU2640931C1) ↗
Patent (human example and animal data)
Full text reviewed (Russian).
Result detail: 1.0 g suppositories containing the tetrapeptide with dimethyl sulfoxide. Claim 1 gives 0.0003–0.0010 g (0.3–1.0 mg) of peptide per suppository, while Example 6 prints 0.0003–0.0010 mg (0.3–1.0 mcg), a 1,000-fold conflict. Example 6: 16 men aged 50–63 with stage I–II BPH, once daily for 10–40 days, versus 5 men on other medicines; assessed by questionnaire; about 10–13% smaller adenoma on ultrasound in 4 men on the highest dose and longest course; libido up in 52%. Rabbits given a single 5 mg/kg rectal dose had no deaths. Says the suppositories are “stable on storage”.
- 35
CIALIS (tadalafil) tablets: prescribing information ↗
Official label (tadalafil)
Label reviewed: tadalafil is FDA-approved for the signs and symptoms of BPH as well as erectile dysfunction.
- 36
Prostatitis: Inflammation of the Prostate ↗
Health information (government)
Page reviewed: the four types of prostatitis, including chronic prostatitis or chronic pelvic pain syndrome and bacterial forms.
- 37
Experimental studying of the drug efficiency Prostamax in the therapy of chronic aseptic prostatitis and its complications ↗
Animal study
Full text reviewed.
Result detail: 60 male rats with surgically caused chronic prostatitis (without infection); from day 30, 15 days of Prostamax 20 mcg/kg into a muscle, versus Samprost (a prostate extract) 20 mcg/kg and a saw palmetto extract 50 mg/kg by stomach tube. In this model the operated glands did not grow larger than at baseline; they became denser and more scarred. Prostamax lowered density to baseline and cut the area of collagen fibers more than 2.5-fold versus operated controls, similar to the comparison products. Limitation: The abstract says sexual activity increased, but the paper shows no data for it; a Geropharm employee is a co-author.
- 38
Experimental Study of Efficiency of Tertapeptide Lysil-Glutamyl-Aspartyl-Proline Using the Model of Benign Prostatic Hyperplasia ↗
Animal study
Full text reviewed.
Result detail: 40 ten-month-old male rats given sulpiride for 60 days to enlarge the prostate (more than doubling the mass of its side lobes). Adding the peptide daily into a muscle for 60 days lowered side-lobe mass by 24%, the weight coefficient by 25% and volume by 40% versus sulpiride alone. Limitation: The dose is printed as 20 mg/kg, 1,000 times the 20 mcg/kg of the same group’s 2013 study, and the paper’s wording about the saw palmetto comparison group is inconsistent.
- 39
Effects of short peptides on lymphocyte chromatin in senile subjects ↗
Cell study
Original abstract reviewed: in white blood cells from people aged 75–88 grown in the laboratory, Prostamax loosened tightly packed chromatin near the center of chromosome 1. The donors were not given the peptide.
- 40
Prostamax ↗
Protocol source
Page checked 24 Sep 2026: copies the patent’s 0.01–100 mcg/kg range, displays an unrelated sequence (KGDG-KGDG-DLKDGA) and claims “>10,000 patient-years” of follow-up without a source.
- 41
Либидон 60 (Libidon): пептид для предстательной железы ↗
Product page (different product)
Page checked 24 Sep 2026 (Russian): each capsule contains 10 mg of “peptide complex A-16, peptides of the prostate gland”, an extract, not Prostamax.
- 42
Any experiences with PROSTAMAX? ↗
Community accounts
Thread read in full: a user with BPH reports no benefit from 2 months of injections and none from Libidon; another claims continuing benefit from 5 mg twice a day for 20 days.
- 43
Longterm BPH treated with Prostamax peptides ↗
Community accounts
Thread read in full: the original poster reports 5 mg once daily by subcutaneous injection with a wider stream within about 5 days and later says the gland “hasn’t really shrunk”; replies include no effect at 1 mg a day, one report of “tremendous prostate pain”, one user whose PSA rose on the peptide and fell only from about 15 to 13 after stopping, and one who says symptoms returned during several weeks without it.
- 44
Prostamax ↗
Protocol source
Page checked 24 Sep 2026: says “each capsule contains approximately 20 mg of active peptide” for a Russian capsule course, without a label.
- 45
Prostamax ↗
Protocol source
Page checked 24 Sep 2026: 10–20 mg daily by mouth or under the tongue; says it is “approved in Russia as supplement” without a product identifier.
- 46
NANOPEP RESIFLEXIN® Plus (dietary supplement) ↗
Product page (blend)
Page reviewed: capsules combining “Peptide Bioregulator KEDP”, KEDG and KE (Vilon) with arginine and plant extracts, sold for male reproductive function. The label lists amino-acid amounts rather than the amount of each peptide, so the Prostamax content per capsule is not stated.
- 47
Prostamax Dosage Chart: 10-20 Day Course Protocol (2026) ↗
Protocol source
Page checked 24 Sep 2026: about 1–2 mg a day, subcutaneous or into a muscle, for about 10–20 days, following the bioregulator “course” convention; says the figures are self-reported, not clinically established; mixed vial used within 28 days.
- 48
Prostamax ↗
Protocol source
Page checked 24 Sep 2026: “typical research dose 1-2 mg/day” for vials, about a 10-day course.
- 49
Prostamax ↗
Evidence summary website
Page checked 24 Sep 2026: “No human dose is established”; also says the evidence is animal and laboratory only, which misses the patent’s human examples.
- 50
Feasibility of Transport of 26 Biologically Active Ultrashort Peptides via LAT and PEPT Family Transporters ↗
Computer-modelling study
Full text reviewed: KEDP scored among the likelier fits for LAT1, LAT2 and PEPT1 transporters in computer models. No uptake was measured.
- 51
Transport of Biologically Active Ultrashort Peptides Using POT and LAT Carriers ↗
Review with computer modelling
Full text reviewed: in its docking models Prostamax (spelled “Prostomax”) did not show strong binding to the LAT1 transporter, although prostate tissue has a lot of LAT1.
- 52
Prostamax peptide (South Africa) ↗
Seller page
Page checked 24 Sep 2026: sells pens at 0.5, 0.75 or 1 mg a day and also lists nasal sprays; no stability or absorption data for either form.
- 53
Зависимость тканеспецифического действия пептидов от количества аминокислот, входящих в их состав (Tissue-specific action of peptides depends on the number of amino acids they contain) ↗
Tissue-culture study
Full text reviewed (Russian).
Result detail: Prostamax raised the growth index of rat prostate tissue pieces by 25 ± 4% and lowered the share of tissue staining for p53 (0.19 versus 0.73 in controls). In the same program it slowed the growth of tissue from deep brain structures by about 28%.
- 54
Влияние аминокислот, природных и синтетических пептидов на культуру ткани кожи молодых и старых крыс (Effect of amino acids and natural and synthetic peptides on skin tissue cultures from young and old rats) ↗
Tissue-culture study (dissertation)
Full dissertation summary reviewed (Russian): Prostamax also stimulated skin tissue pieces from young rats and was the only four-amino-acid peptide active in skin from old rats.
- 55
Unauthorized injectable peptide drugs seized and sold by Canada Peptide may pose serious health risks ↗
Regulator
Advisory reviewed: Prostamax is named in the list of seized unauthorized injectable peptide drugs; the advisory warns that such products may cause infection or allergic reactions and may not have been made or stored safely.
- 56
ClinicalTrials.gov searches for prostamax, KEDP, Lys-Glu-Asp-Pro, Khavinson and “bioregulator peptide prostate” ↗
Registry search
Searched through the registry’s data service; no Prostamax study (the sequence search returns only unrelated amino-acid matches).
- 57
[Deheterochromatinization of the chromatin in old age induced by oligopeptide bioregulator (Lys-Glu-Asp-Pro)] ↗
Cell study
Full text reviewed (Russian).
Result detail: White blood cells from people aged 75–86, cultured with Prostamax at 0.01 mcg/mL: sister-chromatid exchanges rose from 5.9 to 12.0 per cell and active ribosome-gene regions from 0.95 to 2.5. The authors read this as chromatin opening up; the safety meaning of a doubled exchange rate was not examined.
- 58
Клиническая нейроиммуноэндокринология возраст-ассоциированной патологии предстательной железы (Clinical neuroimmunoendocrinology of age-related prostate disease) ↗
Tissue-culture study (dissertation)
Full dissertation summary reviewed (Russian): Prostamax was tested only on rat prostate tissue pieces in a dish; the author says it was chosen for its “anti-androgenic effects” without presenting data for them. The patients in this work did not receive Prostamax.
- 59
[The use of prostatilen in treating patients with chronic prostatitis] ↗
Related product (extract)
Title record reviewed; shows the older prostate-extract product Prostatilen has its own clinical literature, which does not apply to lab-made Prostamax.
- 60
Peptides and Ageing ↗
Review (developer)
Original abstract reviewed: describes clinical use of peptide preparations extracted from animal organs, including prostate; it does not describe lab-made Prostamax.
- 61
Peptides tissue-specifically stimulate cell differentiation during their aging ↗
Cell study (different peptide)
Original abstract reviewed: the prostate cells in this study were treated with Vesugen (Lys-Glu-Asp), not Prostamax, so it is not Prostamax evidence.
- 62
[The tissue-specific effect of synthetic peptides-biologic regulators in organotypic tissues culture in young and old rats] ↗
Tissue-culture study
Original abstract reviewed: at 0.05 ng/mL, Prostamax increased the growth of small pieces of prostate from young and old rats kept alive in a dish.
- 63
Влияние олигопептидов и аминокислот на культуры тканей молодых и старых крыс (Effect of oligopeptides and amino acids on tissue cultures from young and old rats) ↗
Tissue-culture study (dissertation)
Full dissertation summary reviewed (Russian): Prostamax reduced the growth of tissue from deep brain structures by 28 ± 5% in young rats and 23 ± 3% in old rats.
- 64
Оценка противовоспалительной активности пептидов Простамакс и Кортаген на модели химического отека стопы крыс (Anti-inflammatory activity of Prostamax and Cortagen in a rat paw-swelling model: a good laboratory practice study) ↗
Animal study (conference abstract)
Full abstract reviewed (Russian).
Result detail: 90 male rats in a blinded study; peptides injected into the belly cavity at 10, 100 or 1,000 mcg/kg an hour before an agar injection into the paw. Only 1,000 mcg/kg Prostamax reduced swelling (23% less at 2 hours, 19% less at 4 hours); diclofenac almost completely blocked it. Commissioned and funded by Geropharm.
- 65
Molecular mechanisms of sister-chromatid exchange ↗
Review
Original abstract reviewed: sister-chromatid exchange itself is usually error-free, but because most kinds of DNA damage increase it, it has been used in laboratory toxicology tests as an indicator of possible DNA-damaging substances.
- 66
Microcalorimetric study of human blood lymphocytes culture at presence of copper, cadmium and prostamax ↗
Cell study
Original abstract reviewed: it reports copper and cadmium effects on chromatin but states no result for Prostamax.
- 67
The interaction of amino acids, peptides, and proteins with DNA ↗
Test-tube study
Original abstract reviewed: the short peptides KE, AEDG and KEDP changed the melting temperature of DNA in a test tube.
- 68
Short Peptides Regulate Gene Expression ↗
Computer-modelling study
Full text reviewed: a docking table predicts that Prostamax binds the DNA sequence “attc”. A prediction, not an experiment.
- 69
PROSCAR (finasteride) tablets: prescribing information ↗
Official label (finasteride)
Label reviewed: finasteride lowers PSA by about 50%, so PSA values are doubled when interpreting them after six months of use, and any confirmed rise should be evaluated.
- 70
Drugs@FDA search (openFDA): prostamax and prostamaks ↗
Regulator search
No approved product under either spelling in the brand-name, generic-name or active-ingredient fields.
- 71
Bulk Drug Substances Nominated for Use in Compounding Under Section 503A of the FD&C Act (Categories 1–3) ↗
Regulator
Document searched 24 Sep 2026; Prostamax, KEDP and Lys-Glu-Asp-Pro not listed.
- 72
Certain Bulk Drug Substances for Use in Compounding that May Present Significant Safety Risks ↗
Regulator
Page checked; Prostamax not named.
- 73
21 CFR 216.23: Bulk drug substances that can be used to compound drug products in accordance with section 503A ↗
Regulation
Checked; a full-text eCFR search for “prostamax” returns no results.
- 74
Health Canada Recalls and safety alerts search: prostamax (including archived records) ↗
Regulator search
One result: the 1 August 2025 advisory above.
- 75
Think twice before injecting peptides bought online: unauthorized products can seriously harm you ↗
Regulator
Advisory checked: a general warning on unauthorized injectable peptides; does not name Prostamax.
- 76
Therapeutic Goods (Poisons Standard—June 2026) Instrument 2026 (F2026L00633) ↗
Regulator
Full instrument text searched; no entry for Prostamax or Lys-Glu-Asp-Pro. A live search of the Australian Register of Therapeutic Goods could not be completed.
- 77
Understanding your responsibilities when importing, compounding and supplying unapproved peptide products ↗
Regulator
Page checked (archived copy, July 2026): unapproved peptide products “have not been assessed by the TGA for safety, quality or effectiveness”. Does not name Prostamax.
- 78
TGA warning on the risks of importing unapproved peptide products ↗
Regulator
Page checked (archived copy, July 2026): personal importation is permitted only if goods are clearly and accurately labelled; poorly labelled products make it “impossible to verify their contents”. Does not name Prostamax.
- 79
GOV.UK search: prostamax, prostamaks and KEDP ↗
Regulator search
The search service returned no results for any of the three terms.
- 80
World Anti-Doping Code International Standard: Prohibited List 2026 ↗
Sport rules
Document reviewed; Prostamax not named; category S0 quoted.
- 81
World Anti-Doping Code International Standard: Prohibited List 2027 ↗
Sport rules
Document reviewed; Prostamax not named; S0 examples now include “peptides”.
- 82
Prostate health ↗
Community account
Thread reviewed: a user with BPH reports less pain and fewer night-time trips after Prostamax combined with a bladder bioregulator (Vesilute), following an influencer protocol.
- 83
Any experiences with PROSTAMAX? ↗
Community discussion
Thread read in full: a user starting a course calls it cheap with “nearly no side effects” and promises to report back; no follow-up was posted.
- 84
Тетрапептид, регулирующий уровень глюкозы при сахарном диабете, фармакологическое средство на его основе и способ его применения (Tetrapeptide regulating blood glucose in diabetes mellitus; RU2242241C1) ↗
Patent (human example and animal data)
Full text of the Russian original reviewed.
Result detail: Claims H-Lys-Glu-Asp-Trp-NH2 at 0.1–30 mcg/kg at least once daily. Example 8: 36 diabetes inpatients; 16 given 10 mcg into a muscle daily for 10 days and 4 given 100 mcg tablets twice daily, versus 16 given salt-water injections as placebo; insulin dose lowered in 8 of 16 versus 0 of 16. Alloxan-rat examples. States the peptide has no toxicity, without methods. Inventor data, not peer reviewed.
- 85
Панкраген® (Pancragen) capsules 0.2 g: description based on the manufacturer-approved instruction ↗
Product label
Full text reviewed (Russian): 100 mcg peptide complex AKS-P (lysine, glutamic acid, aspartic acid, tryptophan) per 0.2 g capsule; adults 1–2 capsules 1–2 times daily with meals for 1 month; repeat after 4–6 months; not for use in pregnancy or breastfeeding; store dry and dark at 2–25 °C; shelf life 5 years. Also lists 0.275 g capsules and tablets.
- 86
Pancragen Research, Dosing & Protocols ↗
Protocol source
Page checked; source of the mid and high injection rows (1 mg or 2 mg once daily for 10–20 days, repeated every 4–6 months). Sells the free-acid form; its “up to 40%” glucose claim has no traceable source.
- 87
Эффективность пептидного препарата Панкраген у пожилых больных сахарным диабетом 2 типа (Efficacy of the peptide preparation Pancragen in elderly patients with type 2 diabetes) ↗
Human trial (randomized, open)
Full text reviewed (Russian).
Result detail: 60 screened; 30 adults aged 60–74 on glibenclamide randomized: 16 added 100 mcg by mouth twice daily for 3 weeks, 14 continued glibenclamide alone. Fasting glucose 9.4 to 8.5 mmol/L versus 9.1 to 9.0; glucose after a sugar drink fell 1.1–1.3 mmol/L more (between-group p<0.05); HOMA 8.5 to 6.9 versus 7.8 to 7.5. No placebo or blinding.
- 88
Drugs@FDA search (openFDA): pancragen, pankragen and pancragene ↗
Regulator search
No approved product under any of the searched names (brand and generic name fields).
- 89
Peptide substance revealing an immunogeroprotective effect, pharmaceutical composition on its base and the method of its application (US8057810B2) ↗
Patent (human series and animal data)
Full text reviewed (US grant and WO publication).
Result detail: Claims H-Glu-Asp-Pro-OH (C14H21N3O8, 359.33 without counter-ion; acetate salt) at 0.01–100 mcg/kg at least once daily. Examples: rat thymus and spleen tissue, mouse macrophages, a human thymus epithelial cell line, lymphocytes from 95 people aged 75–88, irradiated rats (0.5 mcg per rat daily for 10 days), toxicity in male mice, rats and guinea pigs, and 38 older adults versus 32 controls given 10 mcg or 5 mg intramuscularly daily for 10 days (82% versus 56%). Inventor data, not peer reviewed; no allocation method; per-dose group sizes not given.
- 90
Свидетельство о государственной регистрации RU.77.99.88.003.R.002096.08.25: БАД «КРИСТАГЕН®» (state registration certificate for the dietary supplement Crystagen) ↗
Supplement registration
Scanned certificate reviewed (Russian); read from a seller-hosted copy, not the live register.
Result detail: Tablets (0.215 g and 0.08 g) and capsules (0.215 g) registered as a dietary supplement; adults 1–2 tablets or capsules 1–2 times daily with meals for one month, repeated after 3–6 months; contraindications: individual intolerance, pregnancy, breastfeeding, tendency to bowel disorders (tablets); shelf life 3 years; store dry, protected from light, at 2–25 °C.
- 91
Crystagen Dosing Guide: Half-Life, Reconstitution & Protocol ↗
Protocol source
Page checked; describes about 1–2 mg a day for about 10 days for vials and warns not to convert capsule counts into vial milligrams.
- 92
Отчет о результатах клинического изучения биологически активной добавки к пище Кристаген (Report on the clinical study of the dietary supplement Crystagen) ↗
Human report
Full scanned report reviewed page by page (Russian).
Limitation: Unpublished and manufacturer-linked; 40 adults on 1–3 capsules (0.1 mg each) 2–3 times daily for 15–20 days versus 30 on usual care; no random assignment or blinding described; one “before treatment” column for both groups; its CD8 table values are identical to the patent’s.
- 93
Drugs@FDA search (openFDA): crystagen, kristagen, cristagen and thymalin ↗
Regulator search
No approved product under any of the searched names.
- 94
FDA Evaluation of Epitalon-Related Bulk Drug Substances: Epitalon (Free Base) and Epitalon Acetate (Pharmacy Compounding Advisory Committee briefing document) ↗
Regulator
Full document reviewed.
Key points: Epitalon and epithalamin are different substances; both forms not well characterized; limited water solubility; supplier storage statements only; no pharmacokinetic, acute-toxicity or 2-year cancer studies; theoretical cancer concern from telomerase; three human studies found, none in insomnia; FDA proposed not adding either form to the 503A list.
- 95
Epitalon Dosage Chart – Epithalon Protocol ↗
Protocol source
Page checked; 5 mg once daily for 20 days, 4–6 months off; reconstituted: refrigerate and follow product use-by instructions.
- 96
[Normalizing effect of the pineal gland peptides on the daily melatonin rhythm in old monkeys and elderly people] ↗
Human study (randomized, small)
Full Russian text reviewed.
Result detail: Epitalon 10 mcg into a muscle daily at 10 a.m. for 10 days (15 people) versus epithalamin 10 mg every third day, five times (15) and salt water (10). In 12 Epitalon recipients with low pineal function, 3 a.m. blood melatonin rose from 20 to 49 pg/mL. Sleep not measured; blinding not described.
- 97
Pineal-regulating tetrapeptide epitalon improves eye retina condition in retinitis pigmentosa ↗
Human study (not randomized)
Full text reviewed.
Limitation: About 116 patients on 5 mcg per eye daily for 10 days versus 46 on usual care; not randomized; the 90% figure is the authors' combined judgment; side-effect checking not described. (A different PubMed number, 12195243, is sometimes cited for this study; it is an unrelated case report.)
- 98
Pharmacy Compounding Advisory Committee, July 24, 2026 (official FDA livestream recording) ↗
Regulator (meeting recording)
Voting segments reviewed from the recording's captions: 7 yes, 4 no, 1 abstention for Epitalon free base, and the same for Epitalon acetate; 6 yes, 7 no, 1 abstention for each form of emideltide (DSIP). Not certified minutes.
No matching sources
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Updates and corrections
Updated September 24, 2026. This is a full rewrite of Doserly's Prostamax guide. The previous version said no human data or animal prostate studies had been found; this version adds the patent's patient examples, the second company's suppository patent, the 2013 and 2014 rat studies and the 2011 abstracts, including the anti-androgenic signal in rats. It corrects the description of the 2009 laboratory paper, whose abstract reports no Prostamax result, replaces evidence-review websites with primary sources, and adds the June 2026 FDA warning letter and the 2025 Health Canada advisory. It also removes the “5–10 mg for 5–10 days” website line, which is no longer on its source page, explains the products that share the name, and adds PSA and hormone cautions, dated legal status, storage, monitoring, stopping, a comparison table and a searchable source list. The date describes this revision, not a fresh check of every source.
Found an error or a relevant study we missed? Report a correction with the guide title, the specific passage and a supporting source if available. Please leave out personal health records. See our editorial policy for how we handle attribution, evidence limits and corrections.