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oralanabolic

Dimethandrolone Undecanoate

DMAU11β-methyl-19-nortestosterone-17β-undecanoate
600
Anabolic Ratio
200
Androgenic Ratio
1.5d
Half-Life

Novel investigational compound under active clinical development (NIH/Los Angeles Biomedical Research Institute) as a once-daily oral male contraceptive. Uniquely combines androgenic and progestogenic activity — meaning a single agent can fully suppress spermatogenesis without requiring a progestin co-agent. Not available outside clinical trials.

Mechanism of Action

11β-methyl-19-nortestosterone undecanoate. Potent AR and progesterone receptor (PR) agonist. Complete azoospermia achieved via dual AR + PR-mediated LH/FSH suppression in all Phase I subjects. No aromatization. No 5α-reduction to a more active metabolite. Oral bioavailability improved by undecanoate ester and fat absorption.

Dimethandrolone Undecanoate molecule
Molecular structure

Typical Dosing

100 mg
low / week
200 mg
moderate / week
400 mg
high / week

⚠ Warning Flags

  • Investigational only — not approved; not available outside clinical trials
  • Long-term human safety data not yet established

Effect Profile

Muscle Protein Synthesis
7High
Nitrogen Retention
7High
Strength Gains
7High
Red Blood Cell Production
4Low
Fat Loss
5Moderate
Glycogen Storage
6Moderate
Recovery Speed
7High
Collagen Synthesis
4Low

Side Effect Profile

Hormonal Suppression
8Very High
Estrogenic Effects
2Minimal
Androgenic Effects
5Moderate
Cardiovascular Strain
5Moderate
Liver Stress
3Low
Insulin Resistance
3Low
Mood Changes
4Low
Prostate Risk
2Minimal

Research Studies

Dimethandrolone undecanoate shows promise as a male oral contraceptive agent

Ayoub R, et al. · 2017

PubMed

Phase I clinical trial: 28-day oral DMAU at 400 mg/day significantly suppressed LH, FSH, and testosterone in all subjects, with no serious adverse events — the most promising oral male contraceptive candidate to date.

Daily oral dimethandrolone undecanoate in men: pharmacokinetics and reversibility of suppression of the hypothalamic-pituitary-testicular axis

Thirumalai A, et al. · 2019

PubMed

Extended 28-day study confirmed DMAU's complete and reversible gonadal suppression; serum testosterone recovered to normal within 90 days of cessation, demonstrating reversibility important for contraceptive use.