Tesamorelin
FDA ApprovedGrowth Hormone Secretagogues · GHRH Analog
Tesamorelin is an FDA-approved GHRH analog originally indicated for reducing excess abdominal fat in HIV-associated lipodystrophy.
What is Tesamorelin?
Tesamorelin is an FDA-approved GHRH analog originally indicated for reducing excess abdominal fat in HIV-associated lipodystrophy. It is increasingly used off-label in anti-aging medicine for its ability to stimulate natural growth hormone production and reduce visceral fat.
Also known as: TH9507
How Does Tesamorelin Work?
Binds to pituitary GHRH receptors, stimulating physiological growth hormone secretion. Specifically reduces visceral adipose tissue through GH-mediated lipolysis. Improves trunk fat, lipid profiles, and IGF-1 levels.
What is Tesamorelin Used For?
- Visceral fat reduction
- HIV lipodystrophy
- Growth hormone optimization
Potential Side Effects
- Injection site reactions
- Joint pain
- Peripheral edema
- Paresthesia
Contraindications
- Active malignancy
- Pituitary surgery
- Pregnancy
FDA Legal Status
United States — FDA
FDA ApprovedThis peptide requires a prescription from a licensed healthcare provider.
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Frequently Asked Questions
Is tesamorelin FDA-approved?
Quick Facts
- Legal Status (USA)
- FDA Approved
- Evidence Rating
- AStrong Evidence (Multiple RCTs)
- Class / Subclass
- Growth Hormone Secretagogues / GHRH Analog
- Administration
- subcutaneous
- Typical Dosage
- 2mg daily
- Half-Life
- 26-38 minutes
- Brand Names
- Egrifta
- Year Discovered
- 2001
- Approval Year
- 2010
Sources
Last updated: 2026-04-01
Sources & references
Primary sources used for the dosing, mechanism, side-effect, and regulatory claims on this page. Verify time-sensitive information (regulatory status, prescribing details) on the source before relying on it for medical decisions. See our disclaimer.
- PubMed PMID 17973856 — peer-reviewed primary literature on Tesamorelin.
- FDA Drugs@FDA database — search for the current FDA-approved label, indications, and prescribing information for Tesamorelin.
- FDA Federal Register — official notice record for FDA regulatory actions and Category 1 / 503A bulk-substance updates.