Ipamorelin vs Tesamorelin
§ 01 — Attributes
IpamorelinNNC 26-0161
TesamorelinEgrifta
Summary
A selective growth hormone secretagogue that stimulates pulsatile GH release from the pituitary without significantly affecting cortisol, prolactin, or appetite.
An FDA-approved growth-hormone-releasing hormone analogue for HIV-associated lipodystrophy, used off-label for visceral fat reduction and metabolic health.
Mechanism
Ipamorelin binds the ghrelin receptor (GHSR-1a) in the pituitary, triggering growth hormone release. Unlike earlier secretagogues such as GHRP-6, ipamorelin is highly selective and does not induce hunger or stimulate cortisol.
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.
Typical dose
200–300 mcg, 1–3 times daily (research protocols)
1–2 mg subcutaneous daily
Half-life
~2 hours
~26 minutes
Administration
Subcutaneous
Subcutaneous
Regulatory status
research-only
approved
Cheapest in stock
£21 · £4.2/mg via Peptides UK
Not yet listed
Offers tracked
3
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