Tesamorelin vs Tirzepatide
§ 01 — Attributes
TesamorelinEgrifta
TirzepatideMounjaro / Zepbound
Summary
An FDA-approved growth-hormone-releasing hormone analogue for HIV-associated lipodystrophy, used off-label for visceral fat reduction and metabolic health.
A dual GIP and GLP-1 receptor agonist producing the largest sustained weight reductions of any drug currently licensed, averaging 20–22% body weight loss in clinical trials.
Mechanism
Tesamorelin is a stabilised GHRH analogue with a longer half-life than sermorelin. It selectively reduces visceral adipose tissue (VAT) while preserving subcutaneous fat and lean mass.
Tirzepatide activates both GIP and GLP-1 receptors, a combination that appears to amplify glucose-dependent insulin secretion, slow gastric emptying, and suppress appetite beyond what either pathway achieves alone.
Typical dose
1–2 mg subcutaneous daily
2.5 mg weekly, titrated up to 15 mg weekly
Half-life
~26 minutes
~5 days
Administration
Subcutaneous
Subcutaneous once weekly
Regulatory status
approved
approved
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