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Tesamorelin (Visceral Fat)

GHRH analog approved for HIV-associated lipodystrophy. 2mg daily subcutaneous for visceral fat reduction — the documented clinical dose, typically run 12–26 weeks.

Model levels over time

relative units
Model details: Tesamorelin · relative timing

Compare timing and buildup for this compound. The values are not blood concentrations or a measure of strength.

Shows a relative timing scenario; absolute blood concentrations are not calibrated.

Timing assumptions and sources

Single EGRIFTA WR1.28mg SC dose in healthy subjects, same label study. Original2mg Egrifta26/38min values came after14days, not this single-dose WR formulation.

One 1 mg input peaks at 1 relative unit after a single dose. Other amounts scale proportionally; overlapping doses add when accumulation is on. Different compounds use separate relative scales.

Timing half-life used
0.1833333 hours
Absorption half-life assumed
0.06452204 hours
Reference amount for the relative scale
1 mg
  • The faster rate is inferred to match the 0.15 h source-scoped peak time; absorption half-life 0.06452204183467626 h is a mathematical shape parameter, not separately measured.
  • A single 1-unit input has a peak of 1 relative unit; scaling and repeated-dose addition are mathematical assumptions. This normalization is independent of the example dose.
  • Peak/Tmax/tail reconstruction gives AUC1.7866ng·h/mL versus1.172reported (+52.4%); do not call all endpoints reproduced.
  • Either explicitly identify WR in model scope or keep generic formulation relative; never relabel saved2mg inputs as1.28mg.
  • No additional F multiplier because peak includes availability.
  • Source variability is large; means of endpoints need not define one typical individual curve.
  • EGRIFTA WR US label March2025,12.3

    Healthy single1.28mgSC: Cmax3831pg/mL,Tmax.15h,t1/2 11min,AUCinf1172pg·h/mL. WR and SV are not substitutable; exposure at WR1.28mg resembles original Egrifta2mg.

  • Original EGRIFTA label2010,12.3

    Original2mgSC single dose peak2874.6pg/mL in healthy subjects;26min tail reported after14consecutive doses. OriginalSC F<4%, not50%.

tesamorelin-relative-timing-2026-10 · version 1

Model values over time. Rows are sampled dates; columns identify each output and its units.
DateTesamorelin · Relative timing (relative units)
W10 relative units
W22.12886e-39 relative units
W32.12886e-39 relative units
W42.12886e-39 relative units
W52.12886e-39 relative units
W62.12886e-39 relative units
W72.12886e-39 relative units
W82.12886e-39 relative units
W92.12886e-39 relative units
W102.12886e-39 relative units
W112.12886e-39 relative units
W122.12886e-39 relative units
W132.12886e-39 relative units

The chart uses a bounded time grid. Long horizons can miss brief peaks between samples; shorten the horizon to inspect more detail. Chart peaks are sampled values.

Protocol summary

Tesamorelin (Visceral Fat) · 12 weeks starting Oct 15, 26

  • Tesamorelin — 2.00 mg Every day, weeks 0–12

Protocol overview

Category
peptide stack
Duration
12 weeks
Compounds
1
Tags
fat-loss, visceral-fat, ghrh, tesamorelin, peptide

Compounds in this protocol

How to read this protocol

The chart shows available model curves over the 12-week example. Rows whose model is unavailable are retained for context but produce no curve. Read each model’s details for what its line represents; a plotted level does not predict treatment effects or establish a suitable dose.

The peak/trough explorer examines one complete model interval. The single-dose decline explorer is a separate one-dose scenario; it does not calculate this protocol's washout or a safe treatment-change date. The compound comparison shows available model outputs, not equivalent clinical effects.

Educational only. Not medical advice. These examples do not predict individual blood levels.