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In This Guide
  1. What is Tesamorelin?
  2. FDA Approval
  3. Visceral Fat Research
  4. Dosing
  5. Where to Buy

What is Tesamorelin?

Tesamorelin (trade name Egrifta) is a synthetic GHRH analogue — the full 44 amino acid sequence of human GHRH with a trans-3-hexenoic acid group attached. The modification significantly extends its half-life compared to endogenous GHRH while preserving full biological activity. It is FDA-approved for the reduction of excess abdominal fat in HIV-infected adults with lipodystrophy, making it one of the few research peptides with an actual FDA approval and Phase 3 clinical trial dataset.

Notable: Tesamorelin is one of the only growth hormone secretagogues with FDA approval and published Phase 3 clinical trial data specifically on visceral fat reduction. That body of evidence makes it particularly interesting for metabolic and body composition research.

FDA Approval and Clinical Data

EGRIFTA trials demonstrated statistically significant reductions in visceral adipose tissue (VAT) — the metabolically active fat around internal organs that is strongly associated with cardiovascular disease, insulin resistance, and metabolic syndrome. Key trial data:

Visceral Fat Research Context

Visceral fat is not just a cosmetic concern — it is metabolically active tissue that secretes inflammatory cytokines and free fatty acids, contributing to insulin resistance, cardiovascular disease, and systemic inflammation. Reducing visceral fat specifically (rather than subcutaneous fat) has outsized metabolic benefits. Tesamorelin's specific effect on visceral fat through GH optimization makes it a unique research tool compared to other body composition peptides.

Dosing Protocols

Available in 2mg, 5mg, and 10mg vials. Clinical dosing is 2mg daily subcutaneous injection. Research protocols vary; the FDA-approved protocol provides a reliable framework. Reconstitute with bacteriostatic water; administer subcutaneously.

Where to Buy Tesamorelin

UNYX Peptides carries Tesamorelin in multiple vial sizes, US-manufactured at GMP standards in Arizona. Given the high cost of synthesis for the full 44-amino acid sequence, domestic quality manufacturing is particularly important — overseas low-cost tesamorelin has significant risk of truncated sequences or incorrect synthesis.

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