Tesamorelin research peptide – Tesamorelin (Egrifta) is an FDA-approved GHRH(1-44) analogue

Tesamorelin

5.0 (1)

Tesamorelin (Egrifta) is an FDA-approved GHRH(1-44) analogue that stimulates natural growth hormone release to drive visceral fat loss and IGF-1 production.

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Total Price

฿1900

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For research & laboratory use only. Not for human consumption.

Half-Life

~26-38 minutes

Administration Route

Subcutaneous injection

Visceral Fat Reduction

Only peptide FDA-approved specifically for abdominal fat

HIV Lipodystrophy

Approved for antiretroviral-induced lipodystrophy

Cardiovascular Benefit

Reduces triglycerides and carotid IMT alongside fat loss

Effect Timeline

Start — Week 4

Visceral fat reduction begins; GH levels elevated

Week 8

Measurable abdominal fat loss; IGF-1 normalised

Week 16

15–20% visceral fat reduction; triglycerides declining

Week 24

Maximum fat loss achieved; cardiovascular risk markers improved

Mechanism of Action

Tesamorelin is a stabilised analogue of full-length GHRH(1-44), carrying a trans-3-hexenoic acid group on its N-terminus that blocks DPP-IV cleavage and lengthens the circulating half-life to roughly half an hour. It binds the GHRH receptor on pituitary somatotrophs with high affinity and triggers pulsatile growth hormone secretion, which in turn raises hepatic IGF-1 output. The released growth hormone acts on visceral adipocytes through the GH receptor and JAK2-STAT5 signalling, activating hormone-sensitive lipase and increasing lipolysis. Because it amplifies the body's own GHRH pulse rather than supplying exogenous GH, the resulting hormone profile stays physiological and feedback-regulated. Phase 3 trials confirmed marked reduction of visceral adipose tissue (VAT) through this growth-hormone-driven lipolytic pathway.

Scientific Research

Why Researchers Choose Tesamorelin

Tesamorelin is the only growth-hormone-releasing-hormone analogue to win FDA approval (as Egrifta), which makes it the most clinically validated GHRH peptide available for research. Its appeal is that it raises the body’s own pulsatile growth hormone rather than supplying exogenous GH, keeping the hormonal profile physiological and feedback-regulated. Common research uses include:

  • Visceral adipose tissue (VAT) reduction and tissue-selective lipolysis studies
  • Growth hormone and IGF-1 axis investigations using a pulsatile GHRH stimulus
  • Lipid-profile and cardiovascular risk-marker research (triglycerides, carotid IMT)
  • Age-related growth hormone decline and body-composition protocols
  • Cognitive function studies in mild cognitive impairment

Clinical Validation

The tesamorelin Phase 3 programme ran two double-blind, randomised, placebo-controlled trials enrolling a combined total of more than 800 HIV-positive patients with lipodystrophy. The primary endpoint was visceral adipose tissue measured by CT scan, and the active arm achieved roughly 15 to 18 percent VAT reduction against placebo by 26 weeks, alongside meaningful improvements in lipid profiles and patient-reported outcomes. No other GHRH research peptide carries an evidence base of comparable depth.

Mechanism: Growth-Hormone-Driven Visceral Lipolysis

Tesamorelin triggers pulsatile growth hormone release by activating the GHRH receptor on pituitary somatotrophs. The released growth hormone then acts on visceral adipocytes through a defined cascade:

  1. Growth hormone binds the GH receptor and triggers JAK2-STAT5 signalling
  2. Hormone-sensitive lipase (HSL) is activated via the PKA pathway
  3. Lipolysis rises and free fatty acids are released
  4. Adipocyte sensitivity to insulin-stimulated lipogenesis declines

Visceral fat responds more strongly to this growth-hormone-driven lipolysis than subcutaneous fat, which accounts for the tissue-specific reduction seen in the trials.

Expanding Research: Cognition

A 2019 randomised trial (Baker et al., JCEM) reported that tesamorelin improved executive function, verbal memory, and overall cognitive composite scores in older adults with mild cognitive impairment (MCI). The authors proposed that GH and IGF-1 effects on neuronal metabolism and amyloid processing underlie the benefit, pointing to research applications well beyond the approved indication.

Reconstitution and Storage

Reconstitution: use bacteriostatic water; swirl gently until fully dissolved, do not shake. After reconstitution: store refrigerated and use within 30 days.

For research purposes only. Not for human consumption.

Dosing at a Glance

Route

Subcutaneous injection

Frequency

Once daily

Typical research dose

1–2 mg

Calculate dosage

Opens the calculator with this peptide preselected. Research reference only.

Product FAQs

Customer Reviews

5.0 (1)

1mg before bed now and fat is melting away. Great price for this product, Milo, thank you!

Nathan K.
2025-02-14

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