Tesamorelin (Egrifta® / Egrifta SV®)
Tesamorelin makes the pituitary gland release the body's own growth hormone. It is approved for reducing fat around the internal organs in people with HIV and is also being studied in fatty liver disease and memory decline.
44 amino acids. Trans-3-hexenoic acid + GHRH(1-44)NH₂. An analog of growth hormone–releasing hormone. ~5136 Da.
FDA-approved (2010) — HIV-associated lipodystrophy. Phase III (n=412): −15.2% visceral fat over 6 months. A unique mechanism: acts through the GH axis, not through GLP-1. Being studied in MASH and cognitive decline.
Pituitary GHRH receptor → pulsatile secretion of endogenous GH → ↑IGF-1 → activation of hormone-sensitive lipase (HSL) → ↑lipolysis of visceral fat + ↑hepatic β-oxidation. Physiological feedback is preserved (unlike exogenous GH).
Studies used 2 mg SC once daily, every day, without titration, for courses of 26–52 weeks. Per the FDA label — strictly 2 mg/day.
Level A Human clinical trials. There are randomized controlled trials (RCTs), or the compound has been approved by a regulatory agency. The most reliable level. FDA-approved 2010. Many Phase III trials.
Honest caveat: FDA approval only for HIV lipodystrophy. MASH and cognition — off-label Phase II. Arthralgia 13%, edema 6%. Contraindicated in malignant neoplasms.
Research peptides are laboratory reagents (Research Use Only). They are not medicines and are not intended for use in humans or animals.