Batch 001 - Live Allocation
Next Release: Aug 2026
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Compound Reference

GROWTH HORMONE SUPPORTFDA-ApprovedPopularPopular · Visceral Fat & Lean

Tesamorelin

GHRH Analog · 10mg

Vial size
Status
FDA-Approved
Route
SubQ
Half-life
~8 minutes plasma
Class
GHRH analog
MechanismGHRH Receptor Agonism
Cohort128 active prescriptions
Educational reference only - not a prescription or dosing recommendation. Some compounds are investigational or used off-label; suitability, dose, and monitoring are determined by your supervising physician. See Informed Consent & Disclaimer.
V-Series Member
$100 USD/vial
À-la-carte: $110 USD/vial · Save 9%
Vials per allocation
Member total (1×)$100
À-la-carte total$110
Flat per-vial pricing. Quantity is allocated and dispensed within your physician-supervised protocol - not a direct sale.
What this is

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.

Janoshik Verified
HPLC + MS purity, every batch
Independent third-party lab
COA Per Batch
Lot-level certificates published
Labeled vs actual mg disclosed
Protocol Reviewed
Used in V-Series clinical stacks
Phase 1 supervision onboarding
Tesamorelin · Growth hormone support
◆ Certificate of Analysis · Tesamorelin
JANOSHIK ANALYTICALHPLC + MS · Independent third-party
Batch 001 · lot VL-TES-2026-07A

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.

Lot · Tesamorelin-2026-07-30
97.423%
Labeled
5 mg
Actual (HPLC)
4.73 mg
Method
HPLC + MS
Tested
Jul 30, 2026
Endotoxin
not tested for this lot
Heavy metals
not tested for this lot
Verify independently at janoshik.com/verificationPurity - code 9PCF8V7IKJBR
Clinical Overview
Tesamorelin

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.

Endogenous GH Release
GHRH-receptor agonist; stimulates natural pulsatile GH secretion.
Metabolic Effects
FDA-approved for HIV-lipodystrophy; visceral-fat effects.
Physiological Pattern
Preserves natural feedback vs. exogenous GH.
Mechanism
How It Works

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.

Patient Bloodwork Guide
Bloodwork for Growth-Hormone Protocols

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.

Is it working? (Efficacy)
IGF-1The main signal of your overall growth-hormone output across the day.
IGFBP-3The protein that carries IGF-1 - measured alongside it for a clearer picture of how much is active.
Blood sugar & metabolism (watch closely)
Fasting insulinThe earliest warning sign of insulin resistance - it moves before blood sugar does.
HbA1cYour average blood sugar over ~3 months. Especially relevant with Tesamorelin.
Fasting glucoseA routine blood-sugar check.
Keeping side effects in check
ProlactinIpamorelin (the one Vivre uses) is highly selective and rarely affects this; checked as good practice.
Cortisol (AM)A stress-hormone check included for completeness.
Overall safety
hs-CRPA sensitive inflammation marker - confirms recovery, not strain.
CBC & CMPStandard blood count, liver, and kidney panels.
When the tests happen
Baseline (before you start)Full panel - your natural starting point.
Mid-cycle (week 6–8)IGF-1, fasting insulin, prolactin/cortisol - confirm it works, catch sugar drift early.
Post-cycle (4 weeks off)IGF-1 and fasting insulin - confirm natural production recovers.

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.

Technical Profile
Measurable Properties
ClassGHRH analogue
MechanismGHRH-receptor agonism; stimulates endogenous GH/IGF-1 - well-characterised
Terminal half-lifeShort (~25–40 min) but pharmacodynamic effect outlasts plasma presence
MetabolismPeptidase degradation
Evidence baseStrong - approved for a specific indication (HIV-associated lipodystrophy)
Regulatory statusApproved for a specific indication; other use physician-supervised only
Certificate of Analysis (per batch)
Analytical method: UHPLC-MS. Batch COA available on request - link to be populated per shipment.
COA link - pending per batch
Well-characterised approved-class GHRH analogue. Educational only; treatment physician-determined.
§
Clinical Literature
Peer-Reviewed References

Metabolic Effects of a Growth Hormone–Releasing Factor in Patients with HIV

Falutz J, Allas S, Blot K, et al. · 2007 · New England Journal of Medicine 2007;357:2359–2370

Findings

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 has well-characterised evidence for visceral adipose reduction in its approved indication. Use in healthy adults for body composition is off-label and conducted under physician supervision with explicit consent.
Clinical Applications
Indications
  • Visceral fat reduction
  • Lean mass preservation during weight loss
  • Component of metabolic-aesthetic protocols (V-03)
  • Age-related GH decline (off-label)
Pharmacokinetics
Half-Life & Duration of Action
Half-life is how long a compound stays at active plasma concentration in your body. Most peptides in this catalogue have short plasma half-lives - they clear from your bloodstream within hours, sometimes minutes. The long-half-life compounds in this catalogue are the approved-class incretins (Tirzepatide, Semaglutide, Retatrutide), which are designed for once-weekly dosing - that's the molecular engineering choice that makes weekly dosing work.
Plasma Half-Life
~8 minutes plasma (FDA label, single 1.4mg dose, healthy subjects). Up to ~26-38 minutes after multi-day administration. Biological GH/IGF-1 effects persist far longer through downstream GH pulse cascade.
Why this matters for you
If you don't tolerate a compound or need to discontinue a protocol, short-half-life peptides are out of your bloodstream within hours - not days or weeks. That said, the biological effects they initiate (tissue repair signalling, mitochondrial signalling, gene expression changes) often persist longer than the peptide itself, through downstream cellular cascades. This is normal peptide pharmacology and is important context - the molecule clears fast, but the biology takes longer to wind down.
Evidence Base
FDA-approved with established trial data. Off-label longevity use is increasingly studied.
Dosing protocols, administration frequency, and titration schedules are physician-determined at consultation - not published on these public pages. Vivre maintains a separate internal clinical reference for treating physicians.
Featured In
V-Series Protocols Including Tesamorelin
Commonly Paired
Compounds Often Prescribed With Tesamorelin
Clinical co-allocation patterns observed in Vivre's allocation history. Pairings are not prescriptions - the physician determines suitability per patient at consultation.
Incretin Mimetic
Tirzepatide
Base Form · 10mg
◆ metabolic adjunct
Tesamorelin's visceral-fat indication complements incretin-class therapy for body composition outcomes during metabolic protocols. Standard pairing in Vivre's V-03.
View Tirzepatide detail →
Cytoprotective Peptide
BPC-157
Base Form · 5mg
◆ recovery support
BPC-157 co-allocated during GH-axis intervention to support gastric tolerance and systemic recovery signal.
View BPC-157 detail →
READY TO PROCEED

Start with the Biological Audit

Tesamorelin is verified and lot-tested, dispensed following a Biological Audit. The Audit is complimentary for the Batch 001 cohort.

$100 USD/vial
Tesamorelin · Member rate
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DEMO SITE - PRESENTATION PURPOSES ONLY. All protocols verified and lot-tested, dispensed after comprehensive medical evaluation. Compounds sourced from registered cGMP compounding pharmacies. Individual results vary. MSO structures and revenue models are illustrative for partner conversations. Regulatory outcomes reference publicly disclosed FDA processes and are anticipated but not guaranteed.

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