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Tesamorelin

Growth-hormone axis (GHRH analogue)

Egrifta
FDA-approved drug Moderate-caution

Status & caution. FDA-approved (Egrifta) to reduce excess visceral abdominal fat in HIV-associated lipodystrophy. Use outside that indication is off-label. Raises endogenous GH/IGF-1; carries the metabolic and growth-signalling considerations of the GH axis.

At a glance

Molecular formula
C₂₂₁H₃₆₆N₇₂O₆₇S
Molecular weight
≈5,135.9 g/mol
Sequence / structure
Stabilised analogue of human GHRH(1-44) with an N-terminal trans-3-hexenoyl group.
Regulatory status
FDA-approved drug

Indications & what it's studied for

Approved for HIV lipodystrophy; studied for visceral fat and cognition. Stimulates the pituitary to release growth hormone in a more physiologic, pulsatile way than exogenous GH.

Contraindications & cautions

Active malignancy; pituitary tumour/disruption; pregnancy; hypersensitivity. Caution with diabetes/glucose intolerance (can raise blood glucose).

Commonly reported dosing

Reported, not recommended. The following describes what appears in research literature and community use. It is not a protocol, and unapproved peptides have no validated human dosing.

Approved dosing is a fixed daily subcutaneous injection; reconstituted product is used promptly.

Routes of administration

Subcutaneous injection, typically once daily.

Don't combine with

Glucocorticoids and CYP-affecting drugs may alter response; care alongside insulin/oral hypoglycaemics.

Reported to stack with

Community use pairs GHRH analogues with GH secretagogues (e.g. ipamorelin); this amplifies GH/IGF-1 and the associated unknowns.
Note: "stacking" combines multiple agents and multiplies unknowns; popularity of a combination is not evidence of its safety.

What the research actually shows

Pivotal trials in HIV lipodystrophy support approval; smaller studies explore visceral fat and mild cognitive endpoints.

Before acting on anything here, see Safety & the grey market and how to read a COA.