Growth ⏱ Half-life: Approximately 26-38 minutes.

Tesamorelin

Tesamorelin Acetate

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Half-Life
Approximately 26-38 minutes.
Mol. Weight
5135.83 g/mol

What is Tesamorelin?

Tesamorelin is a stabilized GHRH analog notable for being the only peptide in its class with FDA approval for a therapeutic indication. Clinical data demonstrates targeted visceral fat reduction, making it unique among GH-axis compounds.

Research Applications

Visceral adipose tissue reduction, HIV-associated lipodystrophy, NASH/liver fat research, and cognitive function studies in aging populations.

Dosage Information (Research Use)

Approved clinical dose: 2mg subcutaneously once daily. Research use only.

Reconstitution & Handling

Reconstitute with provided sterile water. Use promptly — less stable than some other GHRH analogs once reconstituted.

Half-Life & Pharmacokinetics

Approximately 26-38 minutes.

Reported Observations in Literature

Clinical trial data: injection site reactions (most common), arthralgia, peripheral edema, myalgia, and paresthesia.

Key Research References

  • Falutz J, et al. “Metabolic effects of a growth hormone-releasing factor in patients with HIV.” N Engl J Med. 2007

How Tesamorelin Works

Tesamorelin is a synthetic GHRH analog consisting of all 44 amino acids of native GHRH with a trans-3-hexenoic acid modification at the N-terminus. This modification provides enhanced stability against enzymatic degradation while maintaining full GHRH receptor agonist activity.

Research Findings

The only GHRH analog with FDA approval for a specific indication (HIV-associated lipodystrophy). Clinical trials demonstrated statistically significant visceral adipose tissue reduction, IGF-1 elevation, and improved trunk fat distribution. Also being studied for NASH/MAFLD and cognitive function in aging.

Dosage & Administration

Approved clinical dose: 2mg subcutaneously once daily. Research use only.

Safety & Side Effects

Clinical trial data: injection site reactions (most common), arthralgia, peripheral edema, myalgia, and paresthesia.

Important: All safety information is derived from published research, primarily animal studies. No controlled human clinical trial data exists unless explicitly noted. This compound is sold for research purposes only.

Quick Facts

Sequence Trans-3-hexenoic acid-modified GHRH(1-44)NH2
Molecular Weight 5135.83 g/mol
Half-Life Approximately 26-38 minutes.
Available Sizes 2mg
Storage Lyophilized: 2-8°C. Reconstituted: use immediately or within 24 hours.

Key Research References

  • Falutz J, et al. "Metabolic effects of a growth hormone-releasing factor in patients with HIV." N Engl J Med. 2007

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