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

REPAIR & RECOVERYInvestigationalMost PrescribedPopular · Vascular & Repair

TB-500

Thymosin Beta-4 · 5mg

Status
Investigational
Route
SubQ
Half-life
~1
Class
Thymosin β4 fragment
WADA
Prohibited (S2)
MechanismActin Sequestration / Angiogenesis
Cohort158 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
$70 USD/vial
À-la-carte: $75 USD/vial · Save 7%
Vials per allocation
Member total (1×)$70
À-la-carte total$75
Flat per-vial pricing. Quantity is allocated and dispensed within your physician-supervised protocol - not a direct sale.
What this is

Synthetic fragment of thymosin beta-4. Promotes vascular scaffolding, cellular migration, and structural tissue repair.

Thymosin Beta-4 · 5mg 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
TB-500 · Repair & recovery
◆ Certificate of Analysis · TB-500
JANOSHIK ANALYTICALHPLC + MS · Independent third-party
Batch 001 · lot VL-TB5-2026-06A

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.

DEMO
Lot · VL-TB5-2026-04A
99.43%
Labeled
5 mg
Actual (HPLC)
5.21 mg
Method
HPLC + MS
Tested
Apr 28, 2026
Endotoxin
not tested for this lot
Heavy metals
not tested for this lot
Clinical Overview
TB-500

TB-500 is a synthetic peptide fragment of Thymosin Beta-4, a 43-amino-acid protein found in nearly all human cells with the exception of red blood cells. The peptide promotes cellular migration, angiogenesis, and tissue repair through actin sequestration.

Cytoskeletal Repair
Regulates actin dynamics to support cell migration and tissue remodeling.
Vascular Support
Promotes new blood-vessel formation at injury sites (preclinical).
Inflammation Modulation
Influences the inflammatory response during recovery.
Mechanism
How It Works

Binds to G-actin, forming a 1:1 complex that inhibits actin polymerization, regulating cytoskeletal dynamics during cell migration and tissue remodeling. Also upregulates VEGF and stimulates endothelial cell migration.

Mechanism & evidence - the honest frame
Mechanism (preclinical): TB-500 is the synthetic fragment of thymosin beta-4, a 43-amino-acid peptide that regulates the actin cytoskeleton - reorganising actin to enable rapid migration of immune and endothelial cells to injury sites, supporting tissue remodeling and angiogenesis. Evidence frame: cellular and animal models only; human tissue-repair efficacy is not established. WADA-prohibited - relevant for any competitive athlete.
Patient Bloodwork Guide
Bloodwork for Recovery & Repair Protocols

Tissue repair / anti-inflammatory - BPC-157, TB-500, KPV, Thymosin, V-01, V-05

These protocols support healing of tendon, ligament, gut, and soft tissue, and calm systemic inflammation. Monitoring tracks inflammation coming down and confirms the body is recovering rather than being strained.

Incremental approach. Vivre uses conservative, course-based dosing - often a defined repair window rather than indefinite use. Markers and imaging confirm progress before extending.

Inflammation
hs-CRPA sensitive marker of systemic inflammation - the key “is it calming down” signal.
IL-6An inflammatory messenger; tracked alongside hs-CRP.
ESRA classic inflammation marker for the bigger picture.
Healing confirmation
Imaging (ultrasound)For tendon/ligament work - confirms structural healing, not just how you feel.
Immune markers (CD4/CD8)Where immune modulation (e.g. Thymosin) is part of the protocol.
Overall safety
CBC & CMPStandard blood count, liver, and kidney panels.
When the tests happen
Baselinehs-CRP, IL-6, ESR + imaging of the target area.
Weeks 4 / 8 / 12hs-CRP, IL-6, ESR - track inflammation trend.
Week 12Repeat imaging to confirm structural healing.

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
ClassSynthetic thymosin β4 fragment
Studied mechanismActin regulation; angiogenesis and cell-migration pathways in preclinical models
Human pharmacokineticsNot well-characterised in peer-reviewed human literature
Evidence basePredominantly preclinical
FormLyophilized powder, reconstituted under clinical protocol
Regulatory statusNot an approved therapy; physician-supervised use 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
Mechanism preclinical; human PK not reliably established. Educational only; not a dosing instruction.
§
Clinical Literature
Peer-Reviewed References
Evidence Synopsis

TB-500 is a synthetic fragment of Thymosin β4, with reproducible preclinical evidence in cardiac and angiogenesis contexts. WADA-prohibited (S2). No human RCT for the fragment specifically.

Cardiac repair
Reproducible preclinical
Mouse and porcine coronary-ligation models (Bock-Marquette 2004, Smart 2007)
WADA S2
Prohibited substance
Peptide hormones and growth factors category
0
Human RCTs for the fragment
Parent Thymosin β4 has limited human ophthalmic/dermal data; TB-500 fragment specifically does not

Thymosin β4 activates integrin-linked kinase and promotes cardiac cell migration, survival and cardiac repair

Bock-Marquette I, Saxena A, White MD, et al. · 2004 · Nature 2004;432:466–472

Findings

Preclinical · Mouse Model. Landmark study showing that Thymosin β4 (the parent peptide of TB-500) administered to mouse hearts after coronary artery ligation activated integrin-linked kinase, promoted cardiomyocyte migration and survival, and improved cardiac function. Established TB4 as a candidate for cardiac repair research. The findings are preclinical (mouse); they catalysed subsequent human-cardiac TB4 research that has not yet produced definitive outcome trials.

View on publisher

Thymosin β4 induces adult epicardial progenitor mobilization and neovascularization

Smart N, Risebro CA, Melville AAD, et al. · 2007 · Nature 2007;445(7124):177–182

Findings

Preclinical · Mouse Model. Demonstrated that systemic Thymosin β4 mobilises adult epicardial progenitor cells and induces neovascularization in mouse models of cardiac injury. Showed stimulated migration of resident endothelial cells, accelerated localised angiogenesis, reduced myocardial scar/fibrosis, and preserved cardiac ejection fraction. Together with Bock-Marquette 2004, this paper established the strongest preclinical case for TB4 as a cardiac-repair candidate. Direct human-cardiac RCT translation has not occurred; ophthalmic and dermal-wound human trials of TB4 (not the TB-500 fragment) exist.

View on publisher

Thymosin beta4 promotes angiogenesis, wound healing, and tissue remodeling

Philp D, Goldstein AL, Kleinman HK · 2004 · Annals of the New York Academy of Sciences 2004;1112:413–423

Findings

In Vitro & Mechanistic Review. Mechanistic review and supporting laboratory data characterising Thymosin β4 as a G-actin sequestering molecule. Identified roles in endothelial cell migration and angiogenesis in wound-healing models. Findings remain primarily preclinical; controlled human trial evidence specific to the TB-500 fragment is limited.

View on publisher
TB-500 (a synthetic fragment of Thymosin β4) has interesting preclinical evidence in cardiac repair and wound-healing contexts. However, no controlled human RCTs of the TB-500 fragment for any indication have been published in major peer-reviewed journals, and TB-500 is not an FDA- or EMA-approved therapy. Important disclosure for competitive athletes: TB-500 is on the World Anti-Doping Agency Prohibited List (S2 - peptide hormones and growth factors). At Vivre, TB-500 is allocated under physician supervision with the evidence limitations and WADA status explicitly disclosed in informed consent.
Clinical Applications
Indications
  • Soft-tissue injury and tendon repair
  • Vascular scaffolding in regenerative protocols
  • Post-surgical wound healing acceleration
  • Hair follicle regeneration in androgenetic alopecia (research-grade)
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
~1.5-3 hours plasma (rodent SubQ; published PK data). Human pharmacokinetics not well-characterised in peer-reviewed literature. Downstream tissue-repair and angiogenic effects persist beyond peptide clearance.
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
Established preclinical research in cardiac, dermal, and corneal repair. Used in equine veterinary medicine. Limited human clinical trial data.
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 TB-500
Commonly Paired
Compounds Often Prescribed With TB-500
Clinical co-allocation patterns observed in Vivre's allocation history. Pairings are not prescriptions - the physician determines suitability per patient at consultation.
Cytoprotective Peptide
BPC-157
Base Form · 5mg
◆ regenerative pair
TB-500 and BPC-157 are the canonical regenerative pairing - TB-500 drives angiogenesis and cellular migration, BPC supports gastric and vascular integrity. Together they form the foundation of Vivre's V-01 tissue-repair protocol.
View BPC-157 detail →
Regenerative Peptide
GHK-Cu
Copper Peptide · 10mg
◆ tissue scaffold
Adds dermal matrix work to TB-500's vascular scaffolding. Relevant when dermal recovery and connective-tissue regeneration both matter - also part of the V-01 stack.
View GHK-Cu detail →
READY TO PROCEED

Start with the Biological Audit

TB-500 is verified and lot-tested, dispensed following a Biological Audit. The Audit is complimentary for the Batch 001 cohort.

$70 USD/vial
TB-500 · 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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