ALarge randomized trials led to FDA approval for reducing HIV-associated belly fat.Large randomized trials in people show a benefit, or a regulator has approved it for a use.
FDA status
FDA-approved
Approved as Egrifta for HIV-associated lipodystrophy only, not for weight loss.
Sport (WADA)
Banned in sport
Prohibited at all times as a growth hormone–releasing factor (S2).
My experience
6/10 out of 10
How well it has worked for me, from 1 to 10. One person's experience, not evidence, and not a recommendation or dosing advice.Read my experience →
Sources for these ratings are cited in the guide below, mainly in Legal status.
At a glance
Sequence
Full 44–amino acid human GHRH sequence, with a hexenoyl (C6) group attached to the first amino acid (tyrosine)
Molecular weight
≈5,136 Da
Formula
C221H366N72O67S
Class
GHRH analog (prescription medicine)
Also known as
Egrifta · Egrifta WR · TH9507
Table of contents8 sections
What is tesamorelin?
Deep in your brain, a hormone called GHRH (growth hormone–releasing hormone) tells your pituitary gland when to release growth hormone. Tesamorelin is a lab-made version of GHRH. It has the same 44 amino acids, plus a small chemical “tail” added to one end [S1] that makes it more stable in the body [1].
Unlike most peptides on this site, tesamorelin is an approved prescription medicine. The US Food and Drug Administration (FDA) approved it in 2010 under the brand name Egrifta [2, S1]. It’s approved for one specific use: reducing excess belly fat in adults with HIV who have lipodystrophy, a change in where the body stores fat [S1].
Why does that matter? Some people on long-term HIV treatment build up visceral fat, the deep belly fat that wraps around the organs. That type of fat is linked to a higher risk of heart disease [3].
How does it work?
Instead of supplying growth hormone directly, tesamorelin works one step earlier. It binds the same receptors as the body’s own GHRH, prompting the pituitary gland to make and release more of its own growth hormone, in natural bursts [S1].
Growth hormone helps the body break down stored fat [S1], and it raises IGF-1, a related hormone that drives many of growth hormone’s effects. In a large trial, IGF-1 levels rose by about 81% [3].
The interesting part is where the fat loss happens. Tesamorelin mainly shrinks deep belly fat while leaving the fat just under the skin largely unchanged [4, 5].
What has research found?
These findings come from human trials, most of them randomized and placebo-controlled (compared with a dummy treatment).
Deep belly fat (the approved use)
The landmark trial: In 412 people with HIV, daily tesamorelin injections for 26 weeks shrank visceral fat by about 15%, while it grew by 5% on placebo. Blood fats improved too, with triglycerides falling sharply [3].
A second large trial: In 404 people, visceral fat fell about 11% at six months and about 18% for those who stayed on it for a year. Waist size and people’s satisfaction with how their belly looked also improved [4].
The big picture: A 2026 analysis that pooled four trials (909 people) confirmed less deep belly fat, smaller waists, less trunk fat, and slightly more lean body mass [6].
The catch: The benefits last only as long as treatment does. When people stopped, the belly fat came back [7].
Liver fat
Fatty liver disease is common in people with HIV, and tesamorelin may help. In a 2014 trial of 50 people, it reduced both belly fat and liver fat [8]. In a 2019 trial of 61 people with HIV and fatty liver disease, liver fat fell by about 37% in relative terms after a year. Over a third of treated patients (35%) got their liver fat back into the normal range, compared with just 4% on placebo [9]. It also worked in people taking modern HIV medicines called integrase inhibitors [10].
Muscle
Among people whose belly fat responded, tesamorelin also increased the size of trunk muscles and reduced the fat stored inside them [11].
Beyond HIV
Obesity: In 60 adults with abdominal obesity and lower-than-normal growth hormone, a year of tesamorelin reduced deep belly fat, triglycerides, and a marker of inflammation. It also slightly reduced the thickness of artery walls, an early sign of heart disease risk [5].
Thinking skills: In 152 older adults, some with mild memory problems, 20 weeks of tesamorelin improved “executive function,” skills like planning and switching between tasks, compared with placebo [1]. A 2025 trial in people with HIV, however, found no clear thinking benefit compared with usual care [12].
How strong is the evidence?
What we know so far
What we still don’t know
Large placebo-controlled trials show it reduces deep belly fat in people with HIV [3, 4]
Whether less belly fat means fewer heart attacks or strokes, because long-term heart safety hasn’t been established [S1]
Pooled analyses from 2026 confirm the main results [6, 13]
Long-term safety, the best dose, and how long benefits last [6]
It reduces liver fat in people with HIV and fatty liver disease [9]
Whether it improves liver health over the long term [9]
How well it works outside HIV, because those trials are still small [1, 5]
A few more things to keep in mind:
Benefits stop when treatment stops. Belly fat returns after people quit [7].
Results vary from person to person. People whose belly fat dropped the most also saw the biggest improvements in blood fats and blood sugar [14].
Funding varies. The drugmaker sponsored some trials [15], but trials funded by the US National Institutes of Health have found benefits too [9].
Safety: what we know
Common side effects: The most frequent are joint pain, redness and itching where it’s injected, pain in the arms or legs, swelling, and muscle aches [S1].
Fluid retention: Growth hormone effects can cause swelling, joint pain, or carpal tunnel syndrome [S1].
Blood sugar: Tesamorelin can affect how the body handles sugar, so the label advises monitoring [S1]. In trials, though, blood sugar generally didn’t worsen, including in a study of people with type 2 diabetes [3, 15].
IGF-1 levels: Because tesamorelin raises IGF-1, doctors monitor it. The effects of keeping IGF-1 high for many years are unknown [S1]. European regulators flagged possible links to cancer and diabetic eye disease as a concern [S2].
Who shouldn’t use it: People who are pregnant, have active cancer, or have a pituitary problem [S1].
Stopping treatment: More people stopped tesamorelin than placebo because of side effects [3, 6].
“Research” products: Tesamorelin sold online as a research chemical isn’t the regulated medicine, and what those products actually contain is uncertain [16].
Legal status
United States: An FDA-approved prescription medicine (brand name Egrifta, including the Egrifta WR formulation) for reducing excess belly fat in adults with HIV-associated lipodystrophy. It’s not approved for weight loss [S1].
Europe: Not approved. The company withdrew its European application in 2012, when the application also covered the UK, after regulators indicated that the benefits didn’t outweigh the risks [S2].
Sports: Banned at all times by the World Anti-Doping Agency (WADA) as a growth hormone–releasing factor [S3].
The bottom line
Tesamorelin is the most thoroughly tested peptide on this site. It’s an approved medicine backed by large, placebo-controlled trials, and it reliably reduces deep belly fat and liver fat in people with HIV. Early studies hint at more, from healthier arteries in people with obesity to sharper thinking in older adults.
The open questions are big ones: whether these changes add up to fewer heart attacks, how well tesamorelin works outside HIV, and what years of use mean for the body. Outside its approved use, sports medicine reviews still consider it investigational [17]. Those questions are exactly what makes tesamorelin worth watching.
References
Peer-reviewed sources indexed in PubMed, numbered in order of first citation. Study type is shown so you can judge how directly each source applies to humans.
1
Baker LD, Barsness SM, Borson S, et al. (2012). Effects of growth hormone–releasing hormone on cognitive function in adults with mild cognitive impairment and healthy older adults: results of a controlled trial. Arch Neurol, 69(11):1420-9.
Falutz J, Potvin D, Mamputu JC, et al. (2010). Effects of tesamorelin, a growth hormone-releasing factor, in HIV-infected patients with abdominal fat accumulation: a randomized placebo-controlled trial with a safety extension. J Acquir Immune Defic Syndr, 53(3):311-22.
Ditta AM, Naeem RM, Sami MM, et al. (2026). Efficacy and Safety of Tesamorelin in People Living With HIV (PLWH) With Lipodystrophy: A Systematic Review and Meta-Analysis. J Int Assoc Provid AIDS Care, 25:23259582261475549.
Falutz J, Allas S, Mamputu JC, et al. (2008). Long-term safety and effects of tesamorelin, a growth hormone-releasing factor analogue, in HIV patients with abdominal fat accumulation. AIDS, 22(14):1719-28.
Stanley TL, Feldpausch MN, Oh J, et al. (2014). Effect of tesamorelin on visceral fat and liver fat in HIV-infected patients with abdominal fat accumulation: a randomized clinical trial. JAMA, 312(4):380-9.
Stanley TL, Fourman LT, Feldpausch MN, et al. (2019). Effects of tesamorelin on non-alcoholic fatty liver disease in HIV: a randomised, double-blind, multicentre trial. Lancet HIV, 6(12):e821-e830.
Adrian S, Scherzinger A, Sanyal A, et al. (2019). The Growth Hormone Releasing Hormone Analogue, Tesamorelin, Decreases Muscle Fat and Increases Muscle Area in Adults with HIV. J Frailty Aging, 8(3):154-159.
Ellis RJ, Vaida F, Hu K, et al. (2025). Effects of Tesamorelin on Neurocognitive Impairment in Persons With HIV and Abdominal Obesity. J Infect Dis, 231(5):1230-1238.
Badran AS, Helal A, Shata KS, et al. (2026). Body composition, hepatic fat, metabolic, and safety outcomes of Tesamorelin, a GHRH analogue, in HIV-associated lipodystrophy: A meta-analysis of randomized controlled trials. Obes Res Clin Pract, 20(1):2-12.
Stanley TL, Falutz J, Marsolais C, et al. (2012). Reduction in visceral adiposity is associated with an improved metabolic profile in HIV-infected patients receiving tesamorelin. Clin Infect Dis, 54(11):1642-51.
Clemmons DR, Miller S, Mamputu JC (2017). Safety and metabolic effects of tesamorelin, a growth hormone-releasing factor analogue, in patients with type 2 diabetes: A randomized, placebo-controlled trial. PLoS One, 12(6):e0179538.
Dominikowski A, Rękoś Z, Olejarz M, et al. (2026). The emerging landscape of performance-enhancing peptides modulating GH-IGF1 axis: bridging the gap between clinical evidence and patient self-administration. Front Endocrinol (Lausanne), 17:1822475.
Villegas Meza AD, Nocek M, Mitchell BC, et al. (2026). Injectable Peptides in Sports Medicine: A Structured Narrative Review of Evidence, Safety, and Antidoping Implications. JBJS Rev, 14(5).