PT-141 vs Tesamorelin
§ 01 — Attributes
PT-141Bremelanotide
TesamorelinEgrifta
Summary
A melanocortin receptor agonist FDA-approved as Vyleesi for hypoactive sexual desire disorder (HSDD) in premenopausal women. Increasingly used off-label by men for libido and arousal.
An FDA-approved growth-hormone-releasing hormone analogue for HIV-associated lipodystrophy, used off-label for visceral fat reduction and metabolic health.
Mechanism
PT-141 (bremelanotide) activates central melanocortin receptors (MC3R/MC4R) rather than the vascular pathway targeted by PDE5 inhibitors like sildenafil. It acts on the brain's sexual-arousal circuitry.
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
1.75 mg subcutaneous on demand
1–2 mg subcutaneous daily
Half-life
~2 hours (effects persist longer)
~26 minutes
Administration
Subcutaneous, Intranasal
Subcutaneous
Regulatory status
approved
approved
Cheapest in stock
£20 · £2.0/mg via Peptides UK
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Offers tracked
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