◂ ALL COMPARISONS

Octreotide vs Tesamorelin

These two sit at opposite ends of the GH axis. Octreotide mimics somatostatin to suppress GH (it is used in acromegaly), while tesamorelin mimics GHRH to stimulate GH release.

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CompareOctreotideTesamorelin10 mg · more sizes
Price—fromR1,199
Cost per mg—R120 / mg
Purity (Janoshik)—On request
Stock—Restocking
Dispatch—When restocked
Certificate—Request CoA
Literature—3 papers →
Research focusGH secretagoguesGHRH-analogue and visceral-fat research
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Prices are read live from the catalogue. Cost per mg is the vial price over its stated mg. Purity is shown only where the certificate is published. Every compound is supplied for laboratory research only.

SIDE BY SIDE

OctreotideTesamorelin
The key differenceSomatostatin analogue — suppresses GHGHRH analogue — stimulates GH
ClassGH secretagoguesGH secretagogues
MechanismOctreotide binds somatostatin receptors (mainly SSTR2), suppressing GH, IGF-1 and many gut hormones.Tesamorelin is a stabilised synthetic analogue of growth-hormone-releasing hormone (GHRH).
StatusApproved for acromegaly and neuroendocrine tumours, with injectable, depot and oral forms; also used in chylothorax and other off-label settings.An approved medicine (US) for excess abdominal fat in HIV-associated lipodystrophy; research use elsewhere.
Reported safety signalsGallstones and gastrointestinal effects are the class-recognised adverse effects; glucose regulation can shift.Label-level trial data exist for its approved indication, including IGF-1 elevation and injection-site effects.
A key studyReviews octreotide’s chemistry, pharmacology, clinical uses and adverse effects. (Clin Pharm 1989, PMID 2653711)A pooled analysis of two phase-3 trials reported that tesamorelin reduced visceral adipose tissue in HIV patients with excess abdominal fat. (J Clin Endocrinol Metab 2010, PMID 20554713)

WHEN TO RESEARCH WHICH

Octreotide models GH suppression and neuroendocrine tumour control; tesamorelin models GH stimulation. Both are discussed here strictly as research compounds; nothing on this page is medical advice or a dosing guide.

FREQUENTLY ASKED

What is the difference between Octreotide and Tesamorelin?

These two sit at opposite ends of the GH axis. Octreotide mimics somatostatin to suppress GH (it is used in acromegaly), while tesamorelin mimics GHRH to stimulate GH release.

What is the regulatory status of Octreotide and Tesamorelin?

Octreotide: Approved for acromegaly and neuroendocrine tumours, with injectable, depot and oral forms; also used in chylothorax and other off-label settings. Tesamorelin: An approved medicine (US) for excess abdominal fat in HIV-associated lipodystrophy; research use elsewhere.

What safety signals have been reported?

Octreotide: Gallstones and gastrointestinal effects are the class-recognised adverse effects; glucose regulation can shift. Tesamorelin: Label-level trial data exist for its approved indication, including IGF-1 elevation and injection-site effects.

Which studies is this comparison based on?

For Octreotide: “Octreotide, a new somatostatin analogue” (PMID 2653711); “Octreotide Subcutaneous Depot for Acromegaly: A Randomized, Double-blind, Placebo-controlled Phase 3 Trial, ACROINNOVA 1” (PMID 39378125); “Treatment of acromegaly with oral octreotide” (PMID 38443224). For Tesamorelin: “Effects of tesamorelin (TH9507), a growth hormone-releasing factor analog, in HIV-infected patients with excess abdominal fat: a pooled analysis of two multicenter, double-blind placebo-controlled phase 3 trials” (PMID 20554713); “Effect of tesamorelin on visceral fat and liver fat in HIV-infected patients with abdominal fat accumulation: a randomized clinical trial” (PMID 25038357); “Effects of tesamorelin, a growth hormone-releasing factor, in HIV-infected patients with abdominal fat accumulation: a randomized placebo-controlled trial with a safety extension” (PMID 20101189).

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