library.onepin.app/proviron-mesterolone Peptide Education Library
Education only, not medical advice 21+ Every dose is an example to finalize with a licensed provider

OnePin Peptide Library · Hormonal

Hormonal Androgen Controlled substance Prescription drug

Proviron (Mesterolone)

Mesterolone

AndrogenOralDHT Derivative1-Methylated (not 17-alpha-alkylated)

Mesterolone, marketed as Proviron, is an orally active androgen derived from dihydrotestosterone (DHT). It is methylated at the 1-alpha position (NOT 17-alpha-alkylated like most oral AAS), which allows oral bioavailability without the classic 17-aa hepatotoxic profile. Developed by Schering in 1934 and introduced clinically in 1966, it remains medically approved in many countries (though not the US since 2006) for male hypogonadism, subfertility, and libido support.

Quick Start
Route
Oral
Start low
25mg
Frequency
1-3x daily
Timing
Take with food or fasted - absorption is adequate either way

Split daily dose into 2-3 evenly spaced doses given the ~12 hour half-life. Typically used throughout a testosterone-based cycle rather than as a standalone compound. Well-tolerated with minimal side-effect burden when used alone.

Start here. Every protocol below is ordered lowest-first. Begin at the smallest effective dose, hold about a week to assess tolerance, and step up only if needed.

Tiered Protocols · lowest first
Quick Start
Conservative start
25mg · Oral · 1-3x daily
Lowest starting point. Hold about a week to assess tolerance before stepping up.
25mg
1-3x daily
Intermediate
SHBG Reduction & Libido
25-50 mg · Oral · Daily
anecdotal · community
25-50 mg
Daily
Research
Male Infertility trial (null result)
75-150 mg/day · Oral · Daily for 6 months
human clinical trial · WHO Task Force 1989 (Int J Androl 12(4):254-264, PMID 2680994)
75-150 mg/day
Daily for 6 months
01

How it works

Mesterolone binds the androgen receptor (AR) with moderate affinity and produces direct androgenic effects similar to DHT. As a DHT derivative, it does not aromatize to estrogen and has no intrinsic estrogenic activity.

Mesterolone binds the androgen receptor (AR) with moderate affinity and produces direct androgenic effects similar to DHT. As a DHT derivative, it does not aromatize to estrogen and has no intrinsic estrogenic activity.

Its most useful pharmacologic feature is strong sex-hormone binding globulin (SHBG) affinity - it binds SHBG tightly, displacing testosterone and raising free (biologically active) testosterone from any co-administered testosterone base. This is why it is a common adjunct in cutting cycles rather than a standalone anabolic.

It also exhibits mild aromatase-competition activity, reducing estrogen conversion from aromatizable compounds (testosterone, methandrostenolone). This does not replace a dedicated aromatase inhibitor at higher testosterone doses but can reduce the required AI dose.

Unlike most oral AAS, mesterolone is 1-alpha-methylated rather than 17-alpha-alkylated. This unusual modification allows oral activity without significant hepatotoxicity - liver enzyme elevation is typically mild. HPT-axis suppression is dose-dependent but generally milder than other AAS.

02

What to expect

Early
Days 1–7

First week: libido effect often noticeable within 3-5 days. Mood may lift slightly. No visible physique change yet.

Mid
Weeks 2–4

Weeks 2-6: subtle muscle hardness improvement, sustained libido effect. Scale weight does not change significantly.

Later
Weeks 4–12

Weeks 7-12: stable effects throughout the cycle. Proviron is a 'background' compound - the benefit is cumulative but never dramatic.

03

Evidence

HumanPresent
AnimalPresent
In-vitroPresent
1989Mesterolone and idiopathic male infertility: a double-blind study. World Health Organization Task Force on the Diagnosis and Treatment of Infertility · WHO Task Force on the Diagnosis and Treatment of Infertility, International Journal of Andrology ↗peer reviewed
1987The effect of mesterolone on sperm count, on serum follicle stimulating hormone, luteinizing hormone, plasma testosterone and outcome in idiopathic oligospermic men · Aafjes JH, Vels JM, Andrologia ↗peer reviewed
1978The effects of mesterolone on the male accessory sex organs, on spermiogram, plasma testosterone and FSH · Comhaire F, Andrologia ↗peer reviewed
1984The effects of mesterolone, a male sex hormone in depressed patients (a double blind controlled study) · Itil TM et al, Progress in Neuro-Psychopharmacology & Biological Psychiatry ↗peer reviewed
04

Interactions & stacking

What's safe to combine, and what belongs in a separate pin.

Keep separate

05

Side effects & safety

Commonly reported

  • Accelerated hair loss in genetically predisposed users (strong DHT effect)
  • Oily skin and acne
  • Mild suppression of endogenous testosterone (dose-dependent)
  • Possible libido surge - sometimes excessive

Less common & notes

  • Prostate enlargement in susceptible users, mood changes, minimal lipid shift (milder than 17-aa orals), very rare hepatic stress markers.
  • Women: contraindicated due to virilization risk at any meaningful dose.
  • Rare: priapism (prolonged erection) at very high doses, exacerbation of prostatic disease.
06

Pharmacokinetics

Illustrative plasma concentration · 24 h
Half-life
~12 hours
Peak · Tmax
1-2 hours
Elimination
2-3 days
Activity
10-14 hours per dose - supports 2-3x daily dosing

Storage. Store at controlled room temperature (20-25°C / 68-77°F). Protect from moisture and light. Keep in original container. Keep out of reach of children and in a locked location - Schedule III controlled substance in the United States.

07

Regulatory status

Schedule III controlled substance in the United States under the Anabolic Steroids Control Act of 1990. FDA approval was withdrawn in 2006 for commercial reasons; the compound was never banned for safety. Remains medically approved in most of Europe, Asia, and Latin America under the Proviron brand (Bayer / Schering) for hypogonadism and subfertility. Possession or distribution without a valid prescription is a federal offense in the United States.

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The guide & community

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