The New England journal of medicine · 2007 · Clinical trial · PMID 18057338
Tesamorelin
Tesamorelin is a synthetic growth hormone-releasing hormone analog. Egrifta products have an FDA-approved indication involving excess abdominal fat in adults with HIV-associated lipodystrophy.
Also indexed as: Egrifta · TH9507
A clear starting point
Tesamorelin is a synthetic growth hormone-releasing hormone analog. Egrifta products have an FDA-approved indication involving excess abdominal fat in adults with HIV-associated lipodystrophy.
Systems mapping shows biological relevance, not a treatment recommendation or a patient CPI score.
No validated chemical structure is displayed in this edition.
How it works
GHRH / GH–IGF-1
Tesamorelin is a synthetic growth hormone-releasing hormone analog. Egrifta products have an FDA-approved indication involving excess abdominal fat in adults with HIV-associated lipodystrophy.
- Targets & processes
- GHRH / GH–IGF-1
- Systems & tissues
- See the pathway description; category links describe research relevance, not demonstrated treatment effects.
What does the evidence show?
Visceral adipose tissue in adults with HIV-associated lipodystrophy.
What this does not establish
The approved indication is reduction of excess abdominal fat in adults with HIV-associated lipodystrophy. It is not a general weight-loss drug; long-term cardiovascular safety is not established.
Citation metadata from PubMed, a service of the U.S. National Library of Medicine, NIH. A citation match is not a guarantee of study quality. Abstracts are not full-text reviews.
Safety is a separate question
Contraindicated in pregnancy, active malignancy, disruption of the hypothalamic-pituitary axis or hypersensitivity. Risks include elevated IGF-1, glucose intolerance and fluid retention.
Contraindications & cautions
Not an exhaustive contraindication review. Contraindicated in pregnancy, active malignancy, disruption of the hypothalamic-pituitary axis or hypersensitivity. Risks include elevated IGF-1, glucose intolerance and fluid retention.
Medication & supplement interactions
Interaction information is incomplete. Contraindicated in pregnancy, active malignancy, disruption of the hypothalamic-pituitary axis or hypersensitivity. Risks include elevated IGF-1, glucose intolerance and fluid retention.
Regulatory status · United States
FDA-approved product · narrow indication. Egrifta products are approved to reduce excess abdominal fat in HIV-infected adults with lipodystrophy, not for general weight management.
Read the official sourceThis is not an exhaustive safety list. Regulatory status varies by jurisdiction and product; investigational use is not approval.
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