— SYNTHETIC GHRH ANALOGUE · LIPOLYTIC HORMONE SECRETAGOGUE

Tesamorelin.

A stabilised analogue of human GHRH, FDA-approved as Egrifta in 2010 for HIV-associated lipodystrophy. The only GHRH analogue to clear Phase III trials with primary endpoint data — and increasingly studied for cognitive preservation and age-related growth hormone decline.

Sequence
44-residue GHRH analogue
Origin
Synthetic (trans-3-hexenoic acid modified)
Developer
Theratechnologies, 2000s
Class
GHRH receptor agonist
Status (UAE)
Research-grade compounding
— THE RESEARCH STORY

The Fat that Finally Had a Name

Native GHRH degrades in under two minutes in plasma. Theratechnologies adds a trans-3-hexenoic acid group to the N-terminus, extending half-life.

Phase III data shows 15–17% visceral fat reduction vs placebo in HIV patients. FDA approves Egrifta — the first and only approved GHRH analogue.

A Phase II trial in HIV patients with mild cognitive impairment finds that IGF-1 restoration via tesamorelin measurably preserves memory function.

— VISCERAL FAT REDUCTION
PHASE III · EGRIFTA TRIAL · % CHANGE IN VAT FROM BASELINE
0% −5% −10% −15% −20% WEEK 0 WEEK 4 WEEK 8 WEEK 13 WEEK 26
TESAMORELIN 2 mg/day PLACEBO CONTROL
— THE MOLECULE

Forty-Four Residues, One Decisive Tweak.

PRIMARY STRUCTURE

Tyr-Ala-Asp-Ala-Ile-Phe-Thr-Asn-Ser-Tyr-Arg
Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys-Leu
Leu-Gln-Asp-Ile-Met-Ser-Arg-Gln-Gln-Gly-Glu
Ser-Asn-Gln-Glu-Arg-Gly-Ala-Arg-Ala-Arg-Leu

C₂₂₁H₃₆₂N₆₆O₇₀S · MW 5135 Da

5135MOLECULAR WEIGHT Da
44AMINO ACIDS
FDA AppvdCLINICAL STAGE

A 44-residue synthetic analogue of GHRH with a trans-3-hexenoic acid modification at the N-terminus — conferring protease resistance and extending plasma half-life to ~26 min vs <2 min for native GHRH.

— AN HONEST READING OF THE DATA

FDA stamped this one.

Phase III endpoint met. Off-label extrapolation remains ahead of the evidence.

TIER 01 / APPROVED USE
Phase III Human Data
  • VAT reduced 15–17% vs placebo
  • IGF-1 normalised in HIV patients
  • Well-tolerated; site reactions only
  • FDA / Health Canada / EMA cleared
  • Lean mass preserved in trial arms
TIER 02 / EMERGING SIGNAL
Phase II Off-Label Data
  • Cognitive preservation (HIV MCI)
  • Memory scores stabilised
  • GH deficiency (non-HIV)
  • Bone density improvements
TIER 03 / SPECULATIVE
Off-Label Longevity Use
  • Anti-aging via IGF-1 restoration
  • Muscle mass gains in healthy adults
  • General metabolic syndrome
  • Athletic performance
— TESAMORELIN MECHANISMS & RESEARCH DOSING READY

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— REGULATORY LANDSCAPE

Prescription in Three Continents.

In the UAE, research-grade peptides occupy a defined regulatory category distinct from licensed medicines. Compounds sold under this classification — including those offered by Dubai Peptides — are intended exclusively for qualified research applications, not for human administration.

Tesamorelin is the only compound in this catalogue with full regulatory approval — cleared by the FDA (2010), Health Canada, and the EMA for HIV-associated lipodystrophy. The Phase III evidence base is robust, with primary endpoints met in controlled trials. Off-label use in longevity medicine — targeting GH deficiency, metabolic syndrome, and cognitive decline — is growing but sits well outside any approved indication.

2010 / FDA APPROVAL

Egrifta (tesamorelin 2mg/day) approved for HIV-associated lipodystrophy — first and only approved GHRH analogue.

2016 / COGNITIVE SIGNAL

Phase II data links IGF-1 restoration to preserved memory function in HIV patients with mild cognitive impairment.

2019–PRESENT / AGE-MANAGEMENT

Off-label prescribing for longevity indications occurs globally, including through UAE compounding pharmacies — distinct from tesamorelin's approved indication.