Tesamorelin Peptide Therapy

Tesamorelin is a stabilized analog of growth hormone-releasing hormone (GHRH). FDA-approved for HIV-associated lipodystrophy; researched off-label in visceral fat reduction.

Plain unbranded photo representing Tesamorelin therapy at Menscape Bangkok
What Tesamorelin may support

What Tesamorelin may support

Tesamorelin is the most clinically validated GHRH analog for visceral adipose tissue reduction, with multiple peer-reviewed trials. Effects on liver fat and lipid profile have also been documented.

Our team confirms baseline metabolic and hormone status before starting, and tracks visceral fat and lipid markers over a 12 to 26-week protocol.

Patient experiences

Tried diet and training for two years without moving belly fat. Tesamorelin protocol with labs every 8 weeks got it moving.

Alexandre, 51

Doctor scoped the visceral fat angle specifically, not just weight. Helped me understand what we were actually treating.

James, 49

Liver enzymes came down alongside the visceral fat. Wasn't expecting that, but the team had flagged it as a possible secondary benefit.

Lucas, 53

Our solutions for Weight‑Loss Management

What BPC-157 is studied for

Indications evaluated in research, listed in order of current evidence weight. Suitability is determined case-by-case.

Visceral fat reduction

Most-studied Tesamorelin indication: clinically meaningful reduction in deep abdominal fat in trials.

Visceral fat reduction

Liver fat (NAFLD)

Research suggests improvements in hepatic steatosis markers alongside visceral fat changes.

Liver fat (NAFLD)

Triglyceride & lipid panel

Documented improvements in triglycerides and other metabolic markers in published studies.

Triglyceride & lipid panel

Cognitive markers (research-stage)

Early studies have explored Tesamorelin in mild cognitive concerns in older adults.

Cognitive markers (research-stage)

What is Tesamorelin?

Tesamorelin is a stabilized analog of growth hormone-releasing hormone (GHRH). FDA-approved for HIV-associated lipodystrophy; researched off-label in visceral fat reduction.

What is Tesamorelin?

How Tesamorelin may work

Tesamorelin is a stabilized GHRH analog with extended half-life. By increasing pulsatile GH release, it acts on visceral adipose tissue and lipid metabolism, with multiple peer-reviewed trials documenting the effect.

How Tesamorelin may work

Who it may be evaluated for

Adults with elevated visceral adiposity or metabolic markers that haven't responded to lifestyle alone. Doctor confirms cardiovascular and glucose-handling status first.

Who it may be evaluated for

How Menscape prescribes Tesamorelin

Baseline metabolic panel, lipid profile, and waist or DEXA measurement are taken. A 12 to 26 week protocol follows, with re-measurement at the midpoint and end.

How Menscape prescribes Tesamorelin

Doctor-led evaluation

Every Tesamorelin protocol starts with a full medical consultation and history review.

Licensed compounding pharmacy

Prescriptions are filled by a licensed compounding pharmacy partner, not over-the-counter.

Monthly monitoring

Follow-up consultations every four to six weeks to assess response and safety.

Research-informed positioning

We frame Tesamorelin as a research-stage peptide and prescribe only when clinically appropriate.

Tesamorelin questions

Is Tesamorelin FDA-approved?

Yes, for HIV-associated lipodystrophy. Use in non-HIV contexts (general visceral fat reduction) is off-label and doctor-supervised.

How is Tesamorelin different from Sermorelin?

Both stimulate endogenous GH. Tesamorelin is stabilized for longer half-life and has stronger clinical data, particularly for visceral fat.

How long until I see results?

Visceral fat changes in trials typically appear by 12 weeks, with continued improvement at 26 weeks. Protocol length depends on goals.

Does it cause water retention?

Mild fluid retention can occur early; the team monitors and adjusts. Severe side effects are uncommon at therapeutic dosing.

What measurements and labs do you take before starting?

Baseline metabolic panel, lipid profile, fasting glucose, IGF-1, and a body-composition measurement (waist circumference or DEXA). These set the baseline for tracking response over 12 to 26 weeks.

Who is not a good candidate?

Patients with active malignancy, untreated diabetes with poor glycemic control, severe cardiovascular disease, or known GHRH hypersensitivity. Each case is reviewed during consultation.

Talk with our medical team about BPC-157

Talk with our medical
team about BPC-157
Talk with our medical team about BPC-157