Tesamorelin
Tesamorelin is a stabilized synthetic analog of GHRH, FDA-approved as Egrifta for HIV-associated lipodystrophy (excess visceral fat). It reduces visceral adipose tissue by 15–20% via sustained GH/IGF-1 elevation. Off-label interest for body composition, anti-aging, and cognitive function — particularly given data suggesting IGF-1 may support hippocampal function. Unlike CJC-1295, it has a defined clinical evidence base from placebo-controlled trials.
Evidence
Moderate evidence
Safety
Unknown safety profile
Clinical Status
Approved
Research Sync
Feb 19, 2026
Dosing
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Pharmacology
Evidence Score
Scores estimated from study counts. Exact breakdown computed after research sync.
Plain-English Snapshot
Tesamorelin is currently categorized as a peptide compound.
Evidence is moderate (71/100): promising signal from 99 indexed studies, but context and population still matter.
Safety scoring is incomplete. Start conservatively and monitor carefully.
Core mechanism
Stabilized GHRH analog binding pituitary GHRH receptors; stimulates GH/IGF-1 production, reducing visceral fat via lipolysis
Practical Context
Strongest current signals
- Level A: Body composition, hepatic fat, metabolic, and safety outcomes of Tesamorelin, a GHRH analogue, in HIV-associated lipodystrophy: A meta-analysis of randomized controlled trials.
- Level B: Effects of Tesamorelin on Neurocognitive Impairment in Persons With HIV and Abdominal Obesity.
- Level B: Effect of tesamorelin on visceral fat and liver fat in HIV-infected patients with abdominal fat accumulation: a randomized clinical trial.