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FDA ApprovedGHRH Analog (1-44) WADA Banned💪 Body Composition

Tesamorelin

Also known as: Egrifta · TH9507

An FDA-approved synthetic GHRH analog originally developed to treat HIV-associated lipodystrophy. Highly effective at reducing visceral adipose tissue.

What is Tesamorelin? An FDA-approved synthetic GHRH analog originally developed to treat HIV-associated lipodystrophy. Highly effective at reducing visceral adipose tissue.

How does Tesamorelin work? Tesamorelin is a 44-amino acid synthetic GHRH analog that stabilizes GHRH against enzymatic degradation. It binds GHRH receptors on the pituitary, increasing GH and subsequently IGF-1. Its primary clinical action is lipolysis of visceral adipose tissue, with studies showing average 17% reductions in visceral fat.

Benefits of Tesamorelin: Significant reduction in visceral fat (average 17% in clinical trials); Improved metabolic markers (triglycerides, HDL); Increased IGF-1 and GH levels; Potential cognitive benefits; FDA-approved for HIV lipodystrophy; Improved body composition

Tesamorelin dosage: Clinical dose is 2mg/day.

Tesamorelin half-life: 26 minutes

Research status: FDA Approved

Source: PeptideWiki — https://www.peptide-wiki.net/peptides/tesamorelin

44 AAs
MW: 5,136 Da
t½: 26 minutes
CAS: 218949-48-5

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Mechanism of Action

Tesamorelin is a 44-amino acid synthetic GHRH analog that stabilizes GHRH against enzymatic degradation. It binds GHRH receptors on the pituitary, increasing GH and subsequently IGF-1. Its primary clinical action is lipolysis of visceral adipose tissue, with studies showing average 17% reductions in visceral fat.

Amino Acid Sequence (44 AAs)

Trans-3-hexenoic acid-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-NH₂

Benefits

  • Significant reduction in visceral fat (average 17% in clinical trials)
  • Improved metabolic markers (triglycerides, HDL)
  • Increased IGF-1 and GH levels
  • Potential cognitive benefits
  • FDA-approved for HIV lipodystrophy
  • Improved body composition

Side Effects & Risks

  • Injection site reactions
  • Peripheral edema
  • Arthralgia
  • Myalgia
  • Potential glucose intolerance
  • Carpal tunnel symptoms

Where to Buy Tesamorelin

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From

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Storage & Reconstitution Guide

Storage Temperature

-20°C lyophilized, 4°C reconstituted

24 months (lyophilized), 28 days (reconstituted)

Reconstitution Solvent

Bacteriostatic water (BAC water)

Swirl gently — do not shake or vortex

Handling Notes

Protect lyophilized peptide from moisture and light. Once reconstituted, keep refrigerated. Discard if solution becomes cloudy or discolored. Use insulin syringe for precise dosing.

Step-by-Step Reconstitution

1

Gather supplies

BAC water, insulin syringe, alcohol swabs, vial

2

Disinfect tops

Swab rubber stoppers of both vials with alcohol

3

Draw BAC water

Pull desired mL of BAC water into syringe

4

Inject slowly

Inject BAC water down the side of the peptide vial, swirl gently to dissolve

Clinical Trials & Human Studies1 trial

🏥 Clinical TrialPhase 3

Phase 3 RCT of Tesamorelin for HIV-Associated Lipodystrophy

Falutz J, et al.·New England Journal of Medicine·2010· n=816·26 weeks

In 816 HIV-positive patients with abdominal lipodystrophy, tesamorelin 2mg/day for 26 weeks reduced visceral adipose tissue by 13.1% vs placebo (-0.5%, p<0.001). Waist circumference decreased 2.4 cm vs 0.3 cm (p<0.001).

Primary Outcome

Visceral adipose tissue area (VAT) change

p-value

<0.001

Igf1 Change

+138 ng/mL vs -9.1 ng/mL

Placebo Vat Change

-0.5%

Waist Circumference

-2.4 cm (tesamorelin) vs -0.3 cm (placebo)

Tesamorelin Vat Change

-13.1%

Molecular Structure

2D molecular structure of Tesamorelin (CAS 218949-48-5), formula C221H366N72O67S — source: PubChem CID 16137828
CAS Number
218949-48-5
PubChem CID
16137828
Molecular Weight
5,136 Da
Mol. Formula
C221H366N72O67S
Amino Acids
44-AA peptide
Wikipedia
View article

Research Protocol

Dose Range
1–2 mg
Frequency
Once daily subcutaneous injection
Cycle
4-12 weeks
Half-Life
26 minutes
Routes
subcutaneous injection
Notes
Clinical dose is 2mg/day.
Open Dosage Calculator →

Legal & Regulatory Status

Research StatusFDA Approved
WADA Status Prohibited
FDA Classification✅ FDA Approved
Originsynthetic

Sold for research purposes only. Not for human use. Laws vary by country.

Commonly Stacked With

View all peptide stacks →

External Resources

PW

PeptideWiki Research Team

Evidence-based research data sourced from PubMed and ClinicalTrials.gov · Last updated: February 25, 2026

Cite: PeptideWiki. “Tesamorelin.” peptide-wiki.net/peptides/tesamorelin. Accessed 2026.

Frequently Asked Questions About Tesamorelin

What is Tesamorelin?

An FDA-approved synthetic GHRH analog originally developed to treat HIV-associated lipodystrophy. Highly effective at reducing visceral adipose tissue.

What are the benefits of Tesamorelin?

Significant reduction in visceral fat (average 17% in clinical trials)

What are the benefits of Tesamorelin?

Improved metabolic markers (triglycerides, HDL)

What are the side effects of Tesamorelin?

Injection site reactions

What is the recommended dosage for Tesamorelin?

Clinical dose is 2mg/day.

How long should a Tesamorelin cycle last?

4-12 weeks

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