Cutting stack (for visceral)
2× Tesamorelin 10mg + Ipamorelin 5mg
4.995.000 ₫
Vial-by-vial breakdown
Tesamorelin is the only growth-hormone–axis compound with peer-reviewed human trial data showing significant, reproducible loss of visceral fat — the deep, metabolically active fat that resists diet and training. Across phase-3 trials, daily Tesamorelin reduced visceral adipose tissue by ~15–18% over 26 weeks versus placebo, with concurrent reduction in liver fat and no adverse effect on fasting glucose. The branded medicine Egrifta is FDA-approved for excess abdominal fat in adults with HIV-associated lipodystrophy; this approval does not apply to VCP research products. Ipamorelin is the ideal partner: a highly selective ghrelin-receptor agonist that adds a clean physiological GH pulse on top of the Tesamorelin GHRH signal — without raising cortisol, prolactin or appetite. Typically dosed nightly during cutting blocks of 8–12 weeks.
Dosage
Start Tesamorelin 1mg + Ipamorelin 100 µg nightly; after 1 week double to Tesamorelin 2mg + Ipamorelin 200 µg nightly
Duration of effect
Tesamorelin ~26 min · Ipamorelin ~2 hours (GH pulse 1–3 h)
See full half-life table →Key Features
- Visceral fat research (GHRH analogue)
- Lean muscle preservation
- No cortisol or prolactin spike
- Improved body composition
Includes key details, half-life data, usage notes and research sources.
Usage Instructions
Subcutaneous injection as recommended. Consult a healthcare professional for protocols tailored to your goals.
Research Highlights
- Backed by scientific research
- Manufactured to pharmaceutical standards
- Used in clinical research settings
- Established safety profile
Safety Information
- •Consult your healthcare provider before use
- •Not intended for pregnant or nursing women
- •Store properly according to instructions
- •Report any adverse effects to your healthcare provider
Source: PLOS One (2015) — Predictors of Treatment Response to Tesamorelin in patients with excess abdominal fat
Clinical Research
Tesamorelin 2 mg/day reduced visceral adipose tissue by ~15–18% over 26 weeks versus placebo, with concurrent reduction in liver fat and no adverse effect on fasting glucose.
Read full studyAdditional Research
Source: Falutz et al., New England Journal of Medicine (2007)
Phase 3 randomised placebo-controlled trial in HIV-associated lipodystrophy: Tesamorelin produced a 15% reduction in visceral adipose tissue at 26 weeks without affecting subcutaneous fat — the strongest human evidence for GHRH-analogue selective visceral fat loss.
Read full studyHuman Clinical Trials
- Tesamorelin in HIV lipodystrophyNew England Journal of Medicine · 2007
412 patients: visceral (deep abdominal) fat fell 15.2% on tesamorelin while rising 5.0% on placebo.
Read the trial412participants