Tesamorelin

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GHRH analog · visceral fat (research)

Synonyms:Tesamorelintesamorelin peptideTesamorelin GHRHvisceral fat peptide
4.9·65 reviews
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Tesamorelin — GHRH analog. FDA-approved (2010) for treating HIV-associated lipodystrophy; available at DOZA as research-grade peptide. LIPO-2009 studies showed visceral fat reduction in HIV patients.

Course12–26 weeks × 1 course/year
Dosage2 mg (1 injection)/day s.c.
ResearchPubMed ↗
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FDA-approved Egrifta protocol (Theratechnologies, 2010): 2 mg subcutaneously once daily. 12-week course provides 15–18% visceral fat reduction, continuation to 26 weeks — result stabilization and IGF-1 improvement by 80–100% from baseline. Evening injection before bed (synchronization with nighttime GH peak). Break between courses 4–6 weeks. Mandatory IGF-1 monitoring.

Free specialist consultation

Benefits

  • Reduces visceral (abdominal) fat by 15–18% over 26 weeks
  • Only FDA-approved peptide in this group (Egrifta, 2010)
  • Doesn't significantly affect subcutaneous fat — targeted action specifically on 'belly fat'
  • Improves metabolic markers: triglycerides, insulin sensitivity
  • Increases IGF-1 by 80–100% from baseline
  • Reduces cardiovascular disease and metabolic syndrome risk
  • Doesn't suppress natural GH production — preserves natural pulsation
  • Has potential in NAFLD/NASH (fatty liver disease)

Who it's for

  • ✔️Those with excess fat concentrated primarily in the abdomen (visceral fat)
  • ✔️For metabolic syndrome and increased cardiovascular risk
  • ✔️After 40 years with natural growth hormone decline
  • ✔️Those combining body correction with hormonal support
  • ✔️For resistance to weight loss by conventional methods and GLP-1
  • ✔️For non-alcoholic fatty liver disease (NAFLD/NASH) — by doctor's prescription

How to take

FDA-approved Egrifta protocol: 2 mg subcutaneously once daily — one injection every evening before bed (synchronization with nighttime GH peak).

Inject into abdomen or front of thigh, rotating injection sites; avoid area around navel.

Course duration of 12 weeks provides clinically significant visceral fat reduction of 15–18%; continuation to 26 weeks — result stabilization.

Break between courses 4–6 weeks. One course per year as standard maintenance.

Mandatory IGF-1 monitoring at start, after 6 weeks and at course end. If IGF-1 above reference — dose adjustment.

Do not mix with other substances in same syringe. Store in refrigerator 2–8°C.

Tesamorelin is a specific pharmaceutical product (Egrifta). Check availability with DOZA consultant.

Before starting — mandatory specialist consultation and analysis of IGF-1, glucose, lipid profile.

Full description

Tesamorelin (brand Egrifta) — synthetic analog of natural GHRH (Growth Hormone-Releasing Hormone), consisting of 44 amino acids. The only peptide in this group approved by FDA (2010) for medical use — for reducing excess visceral (abdominal) fat in patients with HIV-associated lipodystrophy. In this patient group, clinically confirmed visceral fat reduction of 15–18% over 26 weeks and IGF-1 increase of 80–100% from baseline.

Tesamorelin specifically targets visceral fat — the most dangerous type of fat for health, surrounding internal organs and directly associated with cardiovascular disease risk, type 2 diabetes, and metabolic syndrome. Unlike exogenous growth hormone, Tesamorelin preserves natural GH pulsation and doesn't suppress pituitary production.

In studies, Tesamorelin showed potential in visceral fat reduction (15–18% over 26 weeks), improved metabolic markers (triglycerides, insulin sensitivity), increased IGF-1 levels, potential in cognitive functions in HIV patients, and prospects for non-alcoholic fatty liver disease (NAFLD/NASH).

Attention: Tesamorelin is a specific pharmaceutical product (Egrifta by Theratechnologies). Unlike DOZA's main range, it's not available in pre-mixed pen Pen Peptide format. Availability — upon inquiry; cost and protocol are individually coordinated with DOZA consultant.

Mechanism of action

Tesamorelin (Egrifta) — stabilized synthetic analog of GHRH (growth hormone-releasing hormone), 44 amino acids. The only FDA-approved peptide in this group (2010). Binds to GHRH receptor in somatotrophs of anterior pituitary, stimulating natural pulsatile GH release (unlike exogenous GH, preserves physiological pulsation). Elevated GH activates IGF-1 production in liver by 80-100% from baseline (Falutz et al., NEJM 2007). IGF-1 stimulates visceral fat lipolysis through hormone-sensitive lipase activation in adipocytes — selectively acts on abdominal fat, minimally on subcutaneous. Clinical study LIPO-2009 (phase III, n=816): visceral fat reduction of 15-18% over 26 weeks, improved triglycerides and insulin sensitivity. Additional potential: studies in NAFLD/NASH (fatty liver disease — Stanley et al., Lancet HIV 2014) and cognitive impairment.

Side effects & contraindications

Tesamorelin (Egrifta) — the only FDA-approved peptide in this group, safety profile documented in clinical trials. Possible reactions:

• Injection site reactions (redness, swelling, pain) — in 1–5% of cases.

• Temporary fluid retention in first 4–6 weeks — mostly resolves spontaneously.

• Tingling or numbness in extremities — due to water balance changes and IGF-1.

• Muscle, joint pain — in 5–10% of patients.

• Possible blood glucose elevation — caution in diabetes.

• IGF-1 elevation above reference — requires dose adjustment.

Contraindications:

• Active malignancies — GH and IGF-1 potentially stimulate tumor growth.

• Pituitary insufficiency.

• Pregnancy and lactation.

• Diabetic retinopathy, severe diabetes mellitus.

• Severe kidney or liver failure.

• Allergy to drug components (including mannitol).

Mandatory IGF-1 and glucose monitoring during course. Before starting — DOZA specialist consultation and laboratory evaluation.

Scientific research

📄
Read on PubMedPeer-reviewed study

Tesamorelin (Egrifta by Theratechnologies) — the only FDA-approved peptide in this group (2010) for reducing visceral fat in HIV-associated lipodystrophy. Phase III studies confirmed 15–18% visceral fat reduction over 26 weeks, 80–100% IGF-1 increase from baseline, improved triglycerides and insulin sensitivity, preserved natural GH pulsation. Actively studied in non-alcoholic fatty liver disease (NAFLD/NASH), cognitive impairment, and metabolic syndrome. In 2025–2026, transitioned to Category 1 in the US — can be legally compounded by FDA-registered pharmacies by prescription.

Frequently Asked Questions about Tesamorelin

DS

You can buy Tesamorelin on DOZA website. Price is clarified during consultation. Delivery across Ukraine by Nova Poshta in 1–2 days with cold chain 2–8°C.

DOZA Specialist

Client reviews

★★★★★Olena V.November 2025

Tesamorelin — felt the effect after the first week. Fast delivery, everything in thermo-packaging. DOZA — thank you for the support!

★★★★★Andrii S.December 2025

Ordering Tesamorelin for the second course already. Original quality, fair price. DOZA consultant answered all my questions.

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Before/after photos · numbers · timelines · reviews

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Buy Tesamorelin in Ukraine — DOZA

Tesamorelin is available in Ukraine through DOZA online service. GHRH analog · visceral fat (research). We ensure original quality, safe storage and delivery across Ukraine via Nova Poshta. Every order includes a free specialist consultation.

Buy Tesamorelin with 1–2 day delivery across Ukraine. Cold chain 2–8°C. We respond 24/7.

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Olena Kovalchuk

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Updated