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

Tesamorelin (20 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 20 mg vial.

⚡ Quickstart Highlights

Vial contents
20 mg Tesamorelin
Final volume
3 mL
Concentration
6.67 mg/mL
One U-100 unit
66.67 mcg in 0.01 mL

Dosing & Reconstitution Guide

20 mg vial calculations and four reconstitution steps

Phase 3 Research Schedule (3.0 mL = ~6.67 mg/mL)

Research PeriodDaily Dose (mg / mcg)Units (per injection) (mL)
Weeks 1–262 mg / 2000 mcg30 units (0.30 mL)

Frequency: Once daily by subcutaneous injection. Phase 3 trials evaluated 2 mg daily for 26 weeks, with extension data through 52 weeks. This research schedule is distinct from the current EGRIFTA SV label, which uses a different formulation and dose.

Reconstitution Steps

  1. Draw 3.0 mL bacteriostatic water with a sterile syringe.
  2. Inject slowly down the vial wall; avoid foaming.
  3. Gently swirl until dissolved. Do not shake.
  4. Label with the compound, concentration, and preparation date; refrigerate at 2–8 °C (35.6–46.4 °F), protected from light.

Storage note: Bacteriostatic water does not establish a universal use-by period. Follow the exact product label and formulation-specific stability instructions.

Important: This guide is for educational purposes only and is not medical advice.

Supplies Needed

Supply calculations below use the displayed 2 mg once-daily research amount for 8, 12, and 16 weeks.

ItemQuantity
Peptide vials (Tesamorelin, 20 mg each)8 weeks: 6 vials (112 mg total)
12 weeks: 9 vials (168 mg total)
16 weeks: 12 vials (224 mg total)
U-100 insulin syringes8 weeks: 56 syringes
12 weeks: 84 syringes
16 weeks: 112 syringes
Bacteriostatic water (10 mL bottles)Use 3.0 mL per vial.
8 weeks: 18 mL → 2 bottles
12 weeks: 27 mL → 3 bottles
16 weeks: 36 mL → 4 bottles
Alcohol swabsTwo per administration.
8 weeks: 112 swabs — 2 boxes required (100 swabs each)
12 weeks: 168 swabs — 2 boxes required (100 swabs each)
16 weeks: 224 swabs — 3 boxes required (100 swabs each)

Sharps safety: Place used syringes directly into an appropriate sharps container and follow local disposal requirements.

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.

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 ↗