Pooled phase 3 safety study
A 2010 pooled analysis of two placebo controlled phase 3 trials in 806 patients reported visceral fat down 24 percent at 26 weeks with improved lipid measures. Reported in the cited paper.
SourceResearch Use Only. Products listed are not for human or animal consumption. Statements have not been evaluated by the FDA.View full disclaimers →
Tesamorelin is a growth hormone releasing hormone analogue approved as Egrifta for reducing excess abdominal fat in people with HIV associated lipodystrophy. Its entire trial record sits in that population rather than in general body composition use.
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Overview
Tesamorelin is a growth hormone releasing hormone analogue approved as Egrifta for reducing excess abdominal fat in people with HIV associated lipodystrophy. Its entire trial record sits in that population rather than in general body composition use.
What the research reports
Outcomes described across the published Tesamorelin literature and ongoing study. Read each as research context, not a promised result.
Visceral fat reduction study
Pooled phase 3 data reported visceral adipose tissue down 24 percent at 26 weeks, with the reduction sustained through 52 weeks in the same patient cohort.
Liver enzyme study outcome
A 2017 analysis found patients who responded with visceral fat loss also showed greater reductions in ALT and AST liver enzymes. Reported in research settings.
Lipid profile change study
Trials reported improved triglycerides and cholesterol alongside the fat reduction, without a meaningful change in insulin response. Reported in research settings.
Inflammatory marker shift
A 2011 trial reported lower fibrinolytic markers and improved adiponectin in parallel with the loss of visceral fat. Described in the research record.
Physiological GH stimulation
Acts as a GHRH analogue on the pituitary, producing a pulsatile release pattern rather than replacing growth hormone directly. Reported in research settings.
Dosage and protocol
The approved protocol is 2 mg once daily by subcutaneous injection across 12 to 26 weeks. The half-life is 26 to 38 minutes. Figures describe study protocols, not a personal regimen.
Clinical evidence
The published record for Tesamorelin, labeled by strength so you can see what is settled and what is emerging.
A 2010 pooled analysis of two placebo controlled phase 3 trials in 806 patients reported visceral fat down 24 percent at 26 weeks with improved lipid measures. Reported in the cited paper.
SourceA 2008 trial in 410 patients reported an 18 percent visceral fat reduction and lower triglycerides sustained across 52 weeks with good overall tolerability. Reported in the cited paper.
SourceA 2017 analysis of 806 patients reported that those responding with visceral fat loss also showed greater reductions in ALT and AST over 52 weeks. Reported in the cited paper.
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