Metabolic effects of a growth hormone-releasing factor in patients with HIV.
The study demonstrated that tesamorelin treatment for 26 weeks significantly decreased visceral adipose tissue and improved lipid profiles in HIV-infected patients.
Egrifta · TH9507
Tesamorelin is a synthetic analogue of growth hormone-releasing hormone (GHRH) that was approved by the U.S. Food and Drug Administration for the reduction of excess abdominal fat in individuals with HIV-associated lipodystrophy. Researchers primarily study tesamorelin for its effects on body composition and metabolic parameters in this specific patient population. Key findings from clinical trials indicate that tesamorelin significantly reduces visceral fat and improves body fat distribution without exacerbating glycemic control among individuals on integrase inhibitor-based antiretroviral therapy. Despite its established use in HIV-related conditions, current research highlights a lack of robust evidence supporting its application in other therapeutic areas, particularly within orthopaedics and sports medicine. Ongoing studies aim to further elucidate the safety and efficacy of tesamorelin in diverse clinical contexts.
| Formula | C221H366N72O67S |
| Molecular Weight | 5136 g/mol |
| CAS Number | 218949-48-5 |
| PubChem CID | 16137828 |
~4 hours
Not applicable
Poor bioavailability
Subcutaneous administration is the primary route due to its effective bioavailability.
Tesamorelin acts as a growth hormone-releasing hormone (GHRH) analogue, binding to GHRH receptors on pituitary cells, which stimulates the release of endogenous growth hormone (GH). This increase in GH subsequently activates the insulin-like growth factor 1 (IGF-1) signaling pathway, promoting lipolysis and reducing visceral adiposity, particularly in individuals with HIV-associated lipodystrophy. While the precise mechanisms of action and downstream effects are not fully understood, it is known that tesamorelin influences metabolic processes related to fat distribution and energy homeostasis.
1,355
Total Citations
25
Human/RCT
2.5
Avg. Influence
2024
Latest
The study demonstrated that tesamorelin treatment for 26 weeks significantly decreased visceral adipose tissue and improved lipid profiles in HIV-infected patients.
The study demonstrated that lifestyle modifications and careful management of antiretroviral therapies are essential for reducing cardiovascular risk in individuals living with HIV.
Researchers observed that tesamorelin effectively restores normal GH pulsatility and selectively reduces visceral fat in aging men, although its impact on muscle strength and quality of life remains unclear.
Researchers observed that tesamorelin treatment resulted in significant reductions in visceral fat and improvements in body image and lipid profiles in HIV patients over 52 weeks.
Researchers observed that tesamorelin significantly reduced both visceral and liver fat in HIV-infected patients over a 6-month treatment period.
Researchers observed that tesamorelin significantly reduces visceral fat by approximately 18% in HIV-infected patients with central fat accumulation without significant side effects.
Researchers observed that tesamorelin is effective in managing metabolic syndrome in HIV patients, highlighting the need for tailored therapeutic approaches.
Researchers observed that tesamorelin significantly reduced hepatic fat in HIV-infected patients with non-alcoholic fatty liver disease compared to placebo.
The study demonstrated that tesamorelin was well tolerated and resulted in sustained reductions in visceral adipose tissue and triglycerides over 52 weeks in HIV patients.
Researchers observed that the reductive diselenide-selenoester ligation method enables efficient synthesis of tesamorelin and lipidated variants of proteins, enhancing access to challenging biomolecules.
No comprehensive human trials have been conducted to evaluate the efficacy and safety of tesamorelin in orthopaedic applications, leaving its potential benefits in this field largely unvalidated. Additionally, the long-term effects of tesamorelin on body composition and metabolic health in patients with HIV, particularly those on integrase inhibitors, remain unclear, as do the specific mechanisms by which tesamorelin influences tissue regeneration and metabolic processes.
Solubility
Tesamorelin is soluble in water and commonly reconstituted in bacteriostatic water for injection.
Lyophilized
Stable for 2+ years at -20°C, 12 months at 4°C
Reconstituted
Use within 14 days when refrigerated at 4°C
Avoid
Avoid repeated freeze-thaw cycles, direct light
Solvent
Bacteriostatic water or sterile saline recommended
Safety information is derived from published research and may not reflect all known risks. This is not medical advice.
🇩🇪DE
Not approved as a medicinal product. Not a controlled substance. Sale as research chemical is a legal grey area.
🇺🇸US
Approved by the FDA for the treatment of HIV-associated lipodystrophy. Not scheduled by the DEA.
🇦🇺AU
Data limited
🇬🇧UK
Data limited
Legal status information is provided for general reference only and may not reflect the most current regulatory changes. Always verify with official government sources before making any decisions.
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Welli LabsUS | 10mg | $49.99 | $5.00/mg | |
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Eternal PeptidesUS | 10mg | $52.99 | $5.30/mg |
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