Tesamorelin
The visceral-fat GHRH.
- Lyophilised powderFormat
- 10–20 daysVial coverage
- 2 mL BAC waterReconstitution
What it is, in plain language
Tesamorelin is a stabilised analogue of GHRH (growth-hormone releasing hormone), originally developed for HIV-associated lipodystrophy and approved by the FDA (Egrifta) for visceral-fat reduction. Among the GHRH compounds, it is the most clinically validated for targeting visceral adipose tissue specifically.
In research contexts it is studied for visceral-fat reduction, GH/IGF-1 elevation, cognitive function in aging, and metabolic-syndrome models. Effects on subcutaneous fat are modest — Tesamorelin is specifically a visceral-fat compound, not a general fat-loss tool.
Tesamorelin is the most clinically validated GHRH for visceral adipose tissue — and the literature uses extended cycles for a reason.
How it works
Binds the GHRH receptor in the pituitary, producing pulsatile GH release. Molecular stabilisation (an N-terminal trans-3-hexenoic acid group) extends half-life modestly compared to native GHRH, supporting once-daily dosing.
What the literature shows
Multiple clinical trials in HIV-lipodystrophy populations have reported significant reductions in visceral adipose tissue at the 2 mg/day dose. Improvements in cognitive function in aging adults have been reported in smaller studies.
Effects on subcutaneous fat are modest — Tesamorelin is specifically a visceral-fat compound, not a general fat-loss tool. The 26-week trial protocol is the standard the literature is built on; shorter cycles routinely under-deliver on the primary outcome.
Protocol reference
Common research-grade reference figures. Not medical advice — every protocol must be reviewed against the latest published literature and your study design.
Standard 12+ weeks on, 4 weeks off. The visceral-fat literature consistently uses extended cycles (26+ weeks in clinical trials) — shorter cycles under-deliver on the primary outcome. Annual ceiling: 1–2 extended cycles. Pairs with MOTS-c for parallel metabolic work; can be combined with Ipamorelin in some protocols.
2 mL BAC → 10 mg/mL. Draw 0.1 mL = 1 mg; 0.2 mL = 2 mg.
Lyophilised vial: room temperature short-term, refrigerator long-term. Reconstituted: refrigerate; use within 28 days when reconstituted with bacteriostatic water.
Common questions
How is Tesamorelin different from CJC-1295?
Detailed answer coming soon. In the meantime, see the mechanism and protocol sections above, or email hello@aeonco.com.au.
Why is it specifically a visceral-fat compound?
Detailed answer coming soon. In the meantime, see the mechanism and protocol sections above, or email hello@aeonco.com.au.
What is the standard 26-week protocol?
Detailed answer coming soon. In the meantime, see the mechanism and protocol sections above, or email hello@aeonco.com.au.
Can Tesamorelin be combined with Ipamorelin?
Detailed answer coming soon. In the meantime, see the mechanism and protocol sections above, or email hello@aeonco.com.au.
Why are extended cycles necessary?
Detailed answer coming soon. In the meantime, see the mechanism and protocol sections above, or email hello@aeonco.com.au.