Quick facts
- Classification
- GHRH analogue peptide
- Target / mechanism
- Growth hormone-releasing hormone receptor (pituitary)
- Development status
- Marketed for a specific indication; investigated in other settings
- Regulatory status
- FDA-approved
- Evidence level
- Moderate (RCTs, limited scope)
- Therapeutic area
- Endocrine / metabolic
- Route / formulation
- Subcutaneous injection
What it is
Tesamorelin stimulates endogenous growth hormone release rather than supplying growth hormone directly. Its approval is limited to a defined patient population.
How it works
By binding pituitary GHRH receptors it increases pulsatile growth hormone secretion, which in turn raises IGF-1 and influences lipolysis in visceral adipose tissue.
What it has been studied for
- HIV-associated lipodystrophy with excess visceral adiposity
- Investigational work in metabolic liver disease and cognition
Approved uses
- Reduction of excess abdominal fat in adults with HIV-associated lipodystrophy
Safety and side effects
Reported effects include injection-site reactions, arthralgia, peripheral oedema, myalgia, and increases in blood glucose or IGF-1 requiring monitoring.
Warnings and contraindications
Compounded / research status
Investigational uses
Studies in hepatic steatosis and cognitive endpoints have been reported at small scale; these remain investigational.
Frequently asked questions
References
- FDA prescribing informationU.S. Food and Drug Administration
- Pivotal lipodystrophy trialsPeer-reviewed clinical literature
Reference entries are editorial placeholders describing source type and origin. Primary documents are linked as each profile is expanded.
Editorial disclaimer
This site is educational and does not provide medical advice, dosing protocols, or treatment recommendations. Regulatory status and evidence strength differ sharply between compounds. A “research use only” label does not indicate that a product is appropriate for human use. Decisions about medicines belong with a qualified clinician.