Tesamorelin
Tesamorelin
Also known as: Egrifta, TH9507
Overview
Key Facts
Primary Goal: An FDA-approved GHRH analog indicated for the reduction of excess abdominal fat in HIV-infected patients with lipodystrophy
An FDA-approved GHRH analog indicated for the reduction of excess abdominal fat in HIV-infected patients with lipodystrophy. It is a 44-amino acid peptide with a trans-3-hexenoic acid modification that enhances stability. Half-Life 26-38 minutes Typical Dose 1000–2000 mcg Frequency once daily Cycle Length 26 weeks (per FDA labeling), ongoing as prescribed
Dosing Information
Half-Life
26-38 minutes
Typical Dose
1000–2000 mcg
Frequency
once daily
Cycle Length
26 weeks (per FDA labeling), ongoing as prescribed
Administration Routes:
Storage & Reconstitution
Unreconstituted (Powder)
Reconstituted (Mixed)
Research Summary
Tesamorelin received FDA approval in 2010 for HIV-associated lipodystrophy. Phase III trials demonstrated an average 15-18% reduction in visceral adipose tissue over 26 weeks. More recent research has explored its potential cognitive benefits, with a 2020 study showing improvements in executive function and verbal memory in adults at risk for Alzheimer's disease.
Frequently Asked Questions
Common questions about Tesamorelin
UK-Specific Information
Exclusive data points and guidance for UK residents using Tesamorelin
UK Lab Testing
US Lab Testing
Recommended labs: Quest Diagnostics, LabCorp ($120-$200 for peptide safety panel)
Why this matters: UK-specific lab testing guidance not available on US competitor sites
Commonly Stacked With
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Ac-SDKP
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ACE-031
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Acetyl Hexapeptide-3
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AHK-Cu
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Alcohol Prep Pads
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Note: Peptide stacking should only be done under the guidance of a qualified healthcare professional. Individual responses may vary.