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Harm-reduction information only — not medical advice. In crisis or experiencing adverse effects, contact a healthcare professional or your local emergency services immediately.

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Anabolic Steroids/Hormones Human clinical data

Testosterone Undecanoate (Oral)

Jatenzo · Andriol · Oral TU

18.4 hours
Half-life
158–396 mg
Typical dose
Oral, 2×/day
Frequency
Ongoing (TRT)
Cycle length

Oral testosterone (Jatenzo/Andriol) with low lymphatic bioavailability; dosed twice daily with food.

Key takeaways

  • Approved oral testosterone (Jatenzo/Andriol); lymphatic absorption bypasses first-pass liver metabolism.
  • Only ~7% bioavailability and fat-dependent — taken twice daily with food.
  • ~18-hour half-life; the label runs 158–396 mg twice daily, titrated to serum testosterone.
  • Boxed warning for blood-pressure increases; BP monitoring is built into the label.
🚧 Expanded guide coming soon. This compound has PK data and a source — a full overview, mechanism, and dosing guide is pending editorial review.

Reported dosing protocols

Protocols reported in research literature and clinic/community use — informational context, not a dosing recommendation.

Use case Dose Route Frequency Duration
TRT (Jatenzo label) 237 mg start; 158–396 mg titrated Oral, with food Twice daily Ongoing

Pharmacokinetic summary

Model tier
Advanced (t½ + Cmax + Tmax + F)
Half-life
18.4 hours
Cmax
600 ng/dL
Tmax
0.2 days
Bioavailability
7%
Typical dose
158–396 mg

Harm reduction

Aromatizes
Yes
DHT derivative
No
Hepatotoxicity
mild
Injection frequency
Oral, 2×/day

Frequently asked questions

Why is the oral dose so much higher than injectable?

Only about 7% of an oral dose reaches circulation, and that only with dietary fat driving lymphatic uptake. The milligram numbers aren't comparable to injections; titration goes by measured serum testosterone, not by dose.

Is oral testosterone undecanoate liver-toxic like 17-alpha-alkylated orals?

No. The undecanoate ester absorbs through the lymphatics, skipping first-pass hepatic metabolism, which is exactly why it avoids the hepatotoxicity of methyltestosterone-style orals. The dataset's mild hepatotoxicity flag reflects label monitoring, not structural liver risk.

Does timing relative to meals matter?

Yes. Absorption depends on meal fat content, so the label ties every dose to food. Taking it fasted cuts exposure substantially and makes serum levels inconsistent from day to day.

References

Related compounds

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