CalcMyPeptide
Growth Hormone SecretagogueAlso known as: Egrifta

Tesamorelin

GHRH analog FDA-approved (Egrifta) for HIV-associated lipodystrophy; reduces visceral adiposity.

Half-Life
~26-38 minutes
Dose Range
1-2 mg/day
Frequency
1× daily
Vial Sizes
2 mg

🔬 Mechanism of Action

Tesamorelin is a synthetic analog of the full GHRH(1-44) molecule with a trans-3-hexenoic acid modification for enhanced stability. It is the only GHRH analog that is FDA-approved (as Egrifta) for HIV-associated lipodystrophy — the pathological accumulation of visceral adipose tissue.

Tesamorelin stimulates pulsatile GH release from pituitary somatotrophs, leading to increased IGF-1 levels and reduction in visceral fat. Clinical trials demonstrated a 15-18% reduction in visceral adipose tissue. It is increasingly used off-label for body composition optimization in non-HIV populations.

Source: FDA Label (Egrifta), PMID: 20947872

📜Background & History

Tesamorelin (Egrifta) is an FDA-approved synthetic GHRH analog developed by Theratechnologies for lipodystrophy in HIV patients. It is the only GHRH analog approved for human use in the United States. A modified version of native GHRH with the addition of a trans-3-hexenoic acid group for protease stability, it has a longer half-life (~30 min) than native GHRH (~7 min). Clinical trials showed 15–18% reduction in visceral adipose tissue — the most consistent pharmacological reduction of visceral fat demonstrated in clinical trials.

🎯 Research Use Cases

  • HIV-associated lipodystrophy (FDA approved, Egrifta)
  • Visceral adiposity reduction independent of HIV status (off-label research)
  • GH/IGF-1 elevation with physiological pulsatile pattern preservation
  • Cognitive benefits in mild cognitive impairment (Phase II trial data)

💉 Dosing Protocol

Typical Dose1-2 mg/day
Frequency1× daily
Half-Life~26-38 minutes
Common Vial Sizes2 mg

🧪 Reconstitution Example

Vial
2 mg
Water
2 mL
Concentration
1 mg/mL
Per Unit (100u syringe)
10 mcg
Dose of 1000 mcg = 100 units on a 100-unit insulin syringe

⚠️Safety & Considerations

FDA-approved (Egrifta) for HIV lipodystrophy. Generally well-tolerated. May cause injection site reactions, joint pain, and peripheral edema. Contraindicated with active malignancy, pregnancy, and disrupted hypothalamic-pituitary axis. May affect glucose metabolism.

Interactions & Contraindications

GH/IGF-1 elevation affects glucose metabolism — monitor blood glucose. Contraindicated with active malignancy. Not for use in pregnancy. Simvastatin and other glucocorticoids may reduce efficacy.

🔗Synergies & Common Stacks

+ Ipamorelin

Tesamorelin (GHRH analog) + Ipamorelin (GHRP) creates the same synergistic mechanism as Mod GRF + Ipamorelin, with tesamorelin's longer half-life offering slightly more convenience.

+ AOD-9604

Tesamorelin reduces visceral fat via GH stimulation; AOD-9604 directly targets adipose tissue lipolysis. Complementary fat loss mechanisms.

Tesamorelin dosing guide infographic showing dose range 1-2 mg/day, half-life ~26-38 minutes, and reconstitution example
Tesamorelin dosing quick reference — 1-2 mg/day, 1× daily

Frequently Asked Questions

Is Tesamorelin FDA-approved?
Yes — Tesamorelin is FDA-approved as Egrifta for HIV-associated lipodystrophy. It is the only FDA-approved GHRH analog. Off-label use for body composition is common but not officially approved.
What is the Tesamorelin dose?
FDA-approved dose: 2 mg subcutaneously once daily. Some off-label protocols use 1 mg daily. Inject on an empty stomach, preferably at bedtime to align with natural GH pulses.

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