◇ Compound Reference
GHRH Analog · 10mg
GHRH analogue with regulatory-approved evidence for visceral adipose reduction (Falutz et al., NEJM 2007). Used in V-03 for lean-mass preservation during metabolic protocols, and offered as the V-G1 cutting variant for patients whose specific clinical goal is central or visceral fat reduction. Considered the cleaner physiological choice over sustained-action GH secretagogues (e.g. CJC-with-DAC) for patients who want pulsatile, indication-supported GH-axis intervention. Physician-supervised allocation only.
GHRH Analog · 10mg per vial · dispensed after a physician review.
Every 100 units are drawn from one lot and tested once. The certificate below is the one that applies to this batch - when it closes, the next opens with a new lot and a new certificate.
Tesamorelin is a 44-amino-acid synthetic analog of growth hormone-releasing hormone (GHRH). FDA-approved (as Egrifta) for HIV-associated lipodystrophy, where it reduces visceral adipose tissue while preserving lean mass.
Binds GHRH receptors in the anterior pituitary, stimulating endogenous growth hormone secretion in physiological pulses. Distinct from exogenous GH administration in preserving the natural pulsatile pattern.
GHRH / GHRP secretagogues - Tesamorelin, CJC-1295, Ipamorelin, V-G1
These protocols gently restore your body’s own pulsing release of growth hormone rather than replacing it. Because growth hormone also affects blood sugar, monitoring confirms two things: that it is working, and that it is doing so safely.
Incremental approach. Vivre starts below the standard dose and advances only on tolerance. This monitoring is the safety scaffold for that conservative approach.
Educational only - not medical advice or a dosing instruction. Your physician orders the tests, sets your dose, interprets results, and decides if a protocol is right for you. See the Informed Consent & Disclaimer for full terms.
| Class | GHRH analogue |
| Mechanism | GHRH-receptor agonism; stimulates endogenous GH/IGF-1 - well-characterised |
| Terminal half-life | Short (~25–40 min) but pharmacodynamic effect outlasts plasma presence |
| Metabolism | Peptidase degradation |
| Evidence base | Strong - approved for a specific indication (HIV-associated lipodystrophy) |
| Regulatory status | Approved for a specific indication; other use physician-supervised only |
Pivotal Phase 3 RCT in HIV-associated lipodystrophy over 26 weeks. Tesamorelin produced selective reduction in visceral adipose tissue versus placebo, with improvements in lipid profile and no significant glycaemic worsening at the studied dose. This trial supported the FDA approval for the lipodystrophy indication. Use outside this indication is off-label.
View on publisher ↗Tesamorelin is verified and lot-tested, dispensed following a Biological Audit. The Audit is complimentary for the Batch 001 cohort.
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