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Tesamorelin

Egrifta, TH9507

Quick Stats
Studies 64
Trials 24
Score 3
2011 pubmed

Spotlight on tesamorelin in HIV-associated lipodystrophy.

Dhillon. Sohita S

Key Findings

  • In two 26‑week trials, tesamorelin significantly reduced visceral adipose tissue (VAT) in HIV‑associated lipodystrophy.
  • VAT reduction was maintained through 52 weeks if treatment continued, but VAT rebounded after stopping the drug.
  • The drug was well tolerated; serious adverse events occurred in less than 4% of participants, mostly typical growth‑hormone‑related issues.

Practical Outcomes

  • For biohackers interested in cutting visceral fat, tesamorelin shows it can be effective, but it’s currently only approved for HIV patients and requires a prescription. Continuous use is needed to keep the benefits, and stopping the drug leads to fat regain. Expect mild side effects, mainly at the injection site and typical growth‑hormone reactions.

Summary

Tesamorelin is a lab-made hormone that boosts your body’s own growth hormone. In people with HIV who have extra belly fat, it cuts down the deep, dangerous fat around the organs (visceral fat) without much change to the skin‑deep fat. The effect lasts while you keep taking it, but the fat comes back if you stop. Side effects are generally mild, like sore injection spots, joint aches, headaches, or slight swelling.

Abstract

Tesamorelin (Egrifta™) is a synthetic analog of human growth hormone-releasing hormone (also known as growth hormone-releasing factor) that stimulates the synthesis and release of endogenous growth hormone. It is the first and, so far, only treatment indicated for the reduction of excess abdominal fat in patients with HIV-associated lipodystrophy. This article reviews the pharmacological properties, clinical efficacy and tolerability of tesamorelin in patients with HIV-associated central fat accumulation. Subcutaneous tesamorelin was effective in reducing visceral adipose tissue (VAT), but did not affect subcutaneous adipose tissue to a clinically significant extent in two 26-week, well designed, clinical trials in patients with HIV-associated central fat accumulation. This reduction in VAT was maintained in the longer term in patients who continued to receive tesamorelin until week 52 in the extension phases of the two trials. However, discontinuation of therapy during this period resulted in the reaccumulation of VAT. Tesamorelin therapy was also associated with significant improvements in other body composition measures (e.g. trunk fat and waist circumference) and improvements were generally seen in some body image parameters (e.g. belly image distress). Tesamorelin was generally well tolerated, with treatment-emergent serious adverse events occurring in <4% of patients during 26 weeks of therapy. Most of these events were injection-site reactions or events known to be associated with growth hormone therapy (e.g. arthralgia, headache and peripheral edema). Although long-term clinical experience is needed to further assess the benefits and risks of therapy, current evidence suggests that tesamorelin may be useful for reducing visceral adiposity in patients with HIV-associated lipodystrophy, thereby potentially improving self image.

Study Information

Provider

pubmed

Year

2011

Date

2011-12-01T00:00:00.000Z

DOI

10.2165/11208290-000000000-00000

References

13