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Tesamorelin is a synthetic analog of human growth hormone releasing factor (GRF, also called GHRH). It consists of the 44 amino acid human GRF sequence with a hexenoyl group attached to the tyrosine residue at the N terminus. Tesamorelin is the active ingredient of the prescription medicines Egrifta and Egrifta WR. The lyophilized material on this page is a research chemical: it is not Egrifta, it is not Egrifta WR, and no tesamorelin product is currently marketed in Canada.
Tesamorelin is a synthetic peptide analog of human growth hormone releasing factor (GRF, also referred to as growth hormone releasing hormone or GHRH). The FDA label describes it as the 44 amino acid sequence of human GRF carrying a hexenoyl moiety, a six carbon chain with a double bond at position 3, attached to the tyrosine residue at the N terminal part of the molecule. This N terminal modification has been reported to slow degradation by dipeptidyl peptidase 4 (DPP-4) relative to unmodified GRF.
Tesamorelin is an approved prescription medicine in the United States. The FDA approved Egrifta (application 022505, Theratechnologies) on November 10, 2010 as a new molecular entity, and the label indication reads: Egrifta is indicated for the reduction of excess abdominal fat in HIV infected adult patients with lipodystrophy. On March 25, 2025 the FDA approved a supplement to the same application covering Egrifta WR, the more concentrated F8 formulation, for the same indication.
In Canada, Health Canada’s Drug Product Database lists both Egrifta records under Theratechnologies as cancelled. DIN 02438712 is recorded as Cancelled Post Market with a status date of September 30, 2022, and DIN 02423677 is recorded as Cancelled Pre Market with a status date of July 13, 2023. No tesamorelin product is currently authorized for sale in Canada.
The material offered on this page is a laboratory research chemical. It is not Egrifta, it is not Egrifta WR, it is not a licensed or authorized medicine in Canada or any other country, and it is not supplied for any medical purpose.
Published work on tesamorelin concerns the pituitary growth hormone axis:
Every batch of Tesamorelin undergoes:
HPLC and mass spectrometry characterize chemical purity and identity. They do not measure biological activity, and no potency testing is performed or implied.
For laboratory research use only. Not for human or veterinary use.
Further reading