Research use only.  Educational reference. Not medical advice. Not for human consumption.
📈 GHRH Analog

Tesamorelin (10 mg Vial) Dosage Protocol

Tesamorelin is a synthetic analog of growth-hormone-releasing hormone (GHRH) studied for visceral adipose tissue reduction. Approved internationally for HIV-associated lipodystrophy. This page covers the 10 mg vial.

⚡ Quickstart Highlights

Vial size
10 mg
Reconstitution
3 mL BAC water → 3.33 mg/mL
1 U-100 unit =
33.3 mcg
Frequency
Once daily

Dosing & Reconstitution Guide

Route: Subcutaneous  |  Frequency: Once daily  |  Half-life: ~25 minutes (effects last hours)

Standard Approach (3 mL = 3.33 mg/mL)

Reconstituting with 3 mL bacteriostatic water produces a concentration of 3.33 mg/mL. Volume per dose changes with concentration; mg dose itself does not change between vial sizes.

Phase / ProtocolDoseU-100 UnitsVolumeDoses per vial
Week 1 (titration)1 mg30 units0.30 mL10 doses
Weeks 2–12+ (maintenance)2 mg60 units0.60 mL5 doses

Reconstitution Steps

  1. Wipe the vial stopper and BAC water vial with alcohol; let dry.
  2. Draw 3 mL of bacteriostatic water into a sterile syringe.
  3. Inject slowly down the inside glass wall of the peptide vial. Do not aim at the powder.
  4. Gently swirl until fully dissolved. Do not shake.
  5. Label with reconstitution date. Refrigerate at 2–8°C; use within 28 days.

Supplies Needed

Estimates for an 8-week and 12-week cycle at 2 mg per dose, once daily (7 doses/week).

Item8-Week Cycle12-Week Cycle
Tesamorelin (10 mg) vials12 vials17 vials
Insulin syringes (U-100)5684
Bacteriostatic water (10 mL)4 × 10 mL6 × 10 mL
Alcohol swabs1 × 100-pack2 × 100-pack

Protocol Overview

Tesamorelin is the only GHRH analog with dedicated visceral-fat-reduction research. The selectivity for visceral over subcutaneous fat is unusual — most metabolic compounds reduce both. Cycle lengths in HIV-lipodystrophy trials ran 26 weeks; most research-grade protocols run 12–24 weeks.

Effects are gradual — visceral fat measurements typically show change at week 12 with continued reduction through week 26.

Dosing Protocol

Two common dosing intensities:

Cycle structure: 12–24 weeks continuous daily dosing. Visceral fat reduction continues to accumulate through the cycle. Some protocols extend to 52 weeks for sustained effect.

Timing: Evening dosing (pre-bed, within 1h of sleep) aligns with the natural overnight GH pulse. Avoid eating for 1–2 hours after.

Stacking: Sometimes combined with ipamorelin (Tesamorelin + Ipamorelin blend) for amplified GH pulse alongside visceral-fat-targeting effect.

Bloodwork cadence: Fasting glucose and HbA1c every 12 weeks — tesamorelin can mildly worsen glucose tolerance.

Storage Instructions

StateTemperatureDuration
Lyophilized−20°C (−4°F)Up to 24 months, dry & dark
Reconstituted2–8°C (35–46°F)Up to 28 days, protect from light

Important Notes

⚠ Research Use Only: Tesamorelin is approved internationally for HIV-associated lipodystrophy. Use outside this indication is investigational.

How This Works

Tesamorelin is a 44-amino-acid synthetic GHRH analog. A trans-3-hexenoic acid modification at the N-terminus extends bioactive half-life enough for once-daily administration. It binds GHRH receptors on anterior pituitary somatotrophs, stimulating endogenous pulsatile GH release.

Because the action is upstream of GH itself, resulting GH and IGF-1 elevations follow physiological pulsatile patterns rather than the steady-state seen with exogenous GH. Studied effects include selective visceral adipose tissue reduction without comparable effect on subcutaneous fat.

Potential Benefits & Side Effects

Potential Benefits

Side Effect Profile

Lifestyle Factors

Injection Technique

References

1
Falutz J et al. 'Tesamorelin in HIV-infected patients with abdominal fat' — JCEM, 2010 View source ↗
2
Stanley TL et al. 'Tesamorelin on visceral and liver fat in HIV' — JAMA, 2014 View source ↗
3
Stanley TL et al. 'Tesamorelin on NAFLD in HIV' — Lancet HIV, 2019 View source ↗