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Study in humans · 2007 · cited for Tesamorelin

Metabolic effects of a growth hormone-releasing factor in patients with HIV

Falutz J, Allas S, Blot K, Potvin D, Kotler D, Somero M, et al. The New England journal of medicine 2007;357(23):2359-70. doi:10.1056/NEJMoa072375 · PubMed 18057338

In brief

Antiretroviral therapy can drive an accumulation of visceral fat that raises cardiovascular risk. This New England Journal trial gave 412 patients with HIV and excess abdominal fat, 86 percent of them men, a daily injection of tesamorelin (a growth-hormone-releasing-factor analogue) or placebo for 26 weeks, with visceral adipose tissue measured by CT as the primary endpoint. Visceral fat fell 15.2 percent on tesamorelin and rose 5.0 percent on placebo. Triglycerides fell by 50 milligrams per decilitre versus a rise of 9, the total-to-HDL cholesterol ratio fell by 0.31 versus a rise of 0.21, and IGF-I rose 81 percent versus a 5 percent fall. Total and HDL cholesterol also improved. The authors conclude tesamorelin reduces visceral fat in this specific patient group.

Study design

Randomised, double-blind, placebo-controlled trial: 412 people with HIV and treatment-associated abdominal fat, daily subcutaneous tesamorelin or placebo for 26 weeks.

What it does not show

A specific population, HIV-associated lipodystrophy, and 26 weeks of a pharmaceutical product. The study does not address people without HIV, and its lipid changes accompany, rather than replace, standard care.

A clinical trial tests a pharmaceutical form of a compound, in a defined patient group, under medical supervision, with a defined endpoint. None of that transfers to a research-grade vial, and this page does not suggest it does.

Where this paper is cited

  • Tesamorelin — HIV patients with abdominal fat accumulation, 26 weeks: visceral adipose tissue fell about 15% against a rise on placebo.

Other papers cited for Tesamorelin

Further reading

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Research use only This page summarises a published paper. It is not a claim that any product sold by Zyrna Research does what the paper describes, the trial used a pharmaceutical product under medical supervision, and nothing here is dosing guidance. Nothing sold by Zyrna Research is for human or veterinary use.