Tesamorelin (Egrifta)
An FDA-approved GHRH analog that reduces deep belly (visceral) fat in people with HIV-related lipodystrophy.
- Evidence
- Extensive clinical research
- Half-life
- ~30 min
- Sources
- 3 cited
Is tesamorelin FDA-approved?
FDA-approved since 2010 for excess belly fat in HIV lipodystrophy.
Is tesamorelin banned in sport?
Banned in sport by the World Anti-Doping Agency (WADA).
Overview
Tesamorelin is a stabilized form of growth-hormone-releasing hormone (GHRH). It prompts the pituitary to release more of your own growth hormone. In a 26-week phase 3 trial in people with HIV and excess belly fat, visceral fat dropped about 15%, versus a 5% rise on placebo. It's also been studied for fatty liver in people with HIV.
How it works
It binds GHRH receptors in the pituitary, which releases growth hormone in its natural pulses. Growth hormone then raises IGF-1 and helps break down visceral fat.
How long does tesamorelin stay in the body?
About 26–38 minutes, but growth hormone and IGF-1 stay raised much longer.
What it's studied for
- Visceral fat in HIV lipodystrophy
- Fatty liver in HIV
- Body composition
Reported side effects
- Joint pain, muscle pain
- Injection-site redness or itching
- Swelling in hands and feet
- Higher blood sugar
Related: HGH (Somatropin), Sermorelin, Ipamorelin, CJC-1295.
Sources
The studies and prescribing labels this page is written from.
- Metabolic effects of a growth hormone-releasing factor in patients with HIV. N Engl J Med, 2007 PubMed
- Effect of tesamorelin on visceral fat and liver fat in HIV: a randomized trial. JAMA, 2014 PubMed
- Egrifta SV (tesamorelin) prescribing information. DailyMed DailyMed