Skip to content
EntityQ7705415· pop 14· linked from 55 articles

tesamorelin

Sign in to save

Also known as TH9507, N-(trans-3-Hexenoyl)-Human Growth Hormone Releasing Factor (1-44) Acetate, Tesamorelin Acetate, Egrifta

Tesamorelin (INN; trade name Egrifta SV) is a synthetic form of growth-hormone-releasing hormone (GHRH) which is used in the treatment of HIV-associated lipodystrophy, approved initially in 2010. It is produced and developed by Theratechnologies, Inc. of Canada. The drug is a synthetic peptide consisting of all 44 amino acids of human GHRH with the addition of a trans-3-hexenoic acid group.

Research

116 papers

via PubMed

~2 min read

Encyclopedic overview

5 sections
Contents
  • Mechanism of action
  • Contraindication
  • Adverse effects
  • See also
  • References

Tesamorelin (INN; trade name Egrifta SV) is a synthetic form of growth-hormone-releasing hormone (GHRH) which is used in the treatment of HIV-associated lipodystrophy, approved initially in 2010. It is produced and developed by Theratechnologies, Inc. of Canada. The drug is a synthetic peptide consisting of all 44 amino acids of human GHRH with the addition of a trans-3-hexenoic acid group.

== Mechanism of action == Tesamorelin is the N-terminally modified compound based on 44 amino acids sequence of human GHRH. This modified synthetic form is more potent and stable than the natural peptide. It is also more resistant to cleavage by the dipeptidyl aminopeptidase than human GHRH. It stimulates the synthesis and release of endogenous GH, with an increase in level of insulin-like growth factor (IGF-1). The released GH then binds with the receptors present on various body organs and regulates the body composition. This regulation is due to the mixing of anabolic and lipolytic mechanisms. However, it has been found that the main mechanisms by which Tesamorelin reduces body fat mass are lipolysis followed by reduction in triglycerides level.

Excerpted from Wikipedia’s “tesamorelin” article, available under the CC BY-SA 4.0 licence.