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 unitsModel 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
| Date | Tesamorelin · Relative timing (relative units) |
|---|---|
| W1 | 0 relative units |
| W2 | 2.12886e-39 relative units |
| W3 | 2.12886e-39 relative units |
| W4 | 2.12886e-39 relative units |
| W5 | 2.12886e-39 relative units |
| W6 | 2.12886e-39 relative units |
| W7 | 2.12886e-39 relative units |
| W8 | 2.12886e-39 relative units |
| W9 | 2.12886e-39 relative units |
| W10 | 2.12886e-39 relative units |
| W11 | 2.12886e-39 relative units |
| W12 | 2.12886e-39 relative units |
| W13 | 2.12886e-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
- Tesamorelin — 2 mg, every-day
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.