BPC-157 & TB-500 Peptide Blend
99% Purity
Fast Shipping
Lab Tested

BPC-157 & TB-500 Peptide Blend

4.9 (108 reviews)

Key Research Properties:

Third-party tested for purity
Lyophilized powder form
Manufactured in USA
Fast, discreet shipping
SKU: VHL-BPC-TB-001
Purity: 99% (HPLC Verified)
Form: Lyophilized Powder
Storage: Store at -20°C
CAS Numbers: BPC-137525-51-0 / TB-77591-33-4

What is BPC-157 & TB-500 Peptide Blend?

The BPC-157 and TB-500 peptide blend represents a synergistic combination designed for comprehensive tissue repair and recovery research. This formulation combines two of the most extensively studied regenerative peptides into a single, convenient product.

Research indicates that BPC-157 (Body Protection Compound-157), a stable gastric pentadecapeptide, works synergistically with TB-500 (Thymosin Beta-4 fragment) to promote enhanced healing through complementary biochemical pathways[1]. This combination has been the subject of extensive preclinical research demonstrating potential benefits in tissue regeneration, inflammation modulation, and cellular repair processes[2].

BPC-157 (Body Protection Compound)

BPC-157 Chemical Structure - 15 Amino Acid Sequence
  • Derived from gastric protective protein
  • 15 amino acid sequence
  • Promotes angiogenesis (blood vessel formation)
  • Regulates growth factor production
  • Enhances collagen formation

TB-500 (Thymosin Beta-4)

TB-500 Chemical Structure - 43 Amino Acid Thymosin Beta-4 Fragment
  • Naturally occurring peptide in thymus
  • 43 amino acid sequence
  • Actin-binding protein
  • Facilitates cell migration to injury sites
  • Reduces inflammation

Why Combine BPC-157 and TB-500?

Research suggests that BPC-157 and TB-500 work through different but complementary biochemical pathways[3]. When combined, they may offer enhanced benefits for tissue regeneration:

  1. Dual Pathway Activation: BPC-157 works at the gene level to increase actin production[1], while TB-500 helps organize existing actin where it's most needed for cell movement[4].
  2. Enhanced Fibroblast Function: BPC-157 increases growth hormone receptors on fibroblasts, extending their lifespan[5]. TB-500 ensures these cells have adequate actin to make use of their extended functionality.
  3. Comprehensive Healing: Together, they address multiple aspects of tissue repair including angiogenesis, cell migration, collagen production, and inflammation reduction[6].
  4. Synergistic Anti-Inflammatory Effects: Both peptides exhibit anti-inflammatory properties through distinct mechanisms, potentially providing more comprehensive inflammation management[7].

Molecular & Chemical Information

Property BPC-157 TB-500
Molecular Formula C₆₂H₉₈N₁₆O₂₂ C₂₁₂H₃₅₀N₅₆O₇₈S
Molecular Weight 1419.53 g/mol 4963.44 g/mol
Sequence Length 15 amino acids 43 amino acids
CAS Number 137525-51-0 77591-33-4
Sequence Gly-Glu-Pro-Pro-Pro-Gly-Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-Gln-Glu-Lys-Asn-Pro-Leu-Pro-Ser-Lys-Glu-Thr-Ile-Glu-Gln-Glu-Lys-Gln-Ala-Gly-Glu-Ser

Chemical Structure Visualization

Below are the detailed chemical structures of both peptides in this blend. These molecular diagrams illustrate the complete amino acid sequences and their spatial arrangements.

BPC-157 Structure
Complete BPC-157 Chemical Structure - Gly-Glu-Pro-Pro-Pro-Gly-Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val

Molecular Formula: C₆₂H₉₈N₁₆O₂₂
Molecular Weight: 1419.53 g/mol

TB-500 Structure
Complete TB-500 Chemical Structure - Thymosin Beta-4 Fragment (43 Amino Acids)

Molecular Formula: C₂₁₂H₃₅₀N₅₆O₇₈S
Molecular Weight: 4963.44 g/mol

Structural Notes:
  • BPC-157: A stable pentadecapeptide (15 amino acids) with a compact structure that contributes to its resistance to degradation in gastric environments.
  • TB-500: A larger 43-amino acid peptide with an acetylated N-terminus (Ac-Ser), which enhances its stability and biological activity. The structure contains the critical actin-binding domain responsible for its cellular migration effects.

Comparative Analysis

Characteristic BPC-157 TB-500 Combined Blend
Primary Mechanism Angiogenesis, growth factor modulation Actin regulation, cell migration Multi-pathway tissue repair
Tissue Specificity Broad spectrum (GI, musculoskeletal, vascular) Primarily musculoskeletal Comprehensive tissue coverage
Anti-Inflammatory Moderate to Strong Moderate Enhanced
Angiogenic Effects Strong Moderate Optimized
Research Applications Tendon, ligament, GI healing Muscle, cardiac tissue All soft tissue repair
Stability High (stable pentadecapeptide) Good (acetylated N-terminus) Excellent when stored properly

Research Note

The synergistic effects of this combination have been documented in preclinical studies[8], with research suggesting faster healing times and improved structural integrity of repaired tissues when compared to either peptide administered individually.

Quality Assurance & Testing

Every batch of our BPC-157 & TB-500 blend undergoes rigorous third-party testing to ensure pharmaceutical-grade quality:

99%+

Purity

Verified by HPLC

Identity Confirmed

Mass Spectrometry

3rd

Party Tested

Independent Lab

  • HPLC (High-Performance Liquid Chromatography): Verifies purity and concentration
  • Mass Spectrometry: Confirms molecular weight and peptide identity
  • Amino Acid Analysis: Validates complete sequence accuracy
  • Endotoxin Testing: Ensures levels are within acceptable limits
  • Sterility Testing: Confirms absence of microbial contamination

Mechanism of Action: Synergistic Healing

Understanding the distinct yet complementary mechanisms of BPC-157 and TB-500 is crucial for appreciating their synergistic potential in tissue repair research.

Actin Regulation and Cell Migration

Successful wound healing depends heavily on cell migration to injury sites. Fibroblasts, immune cells, and other reparative cells must migrate efficiently to damaged tissue[9]. Both peptides influence actin, the protein responsible for cell movement, but through different mechanisms:

BPC-157's Role:

Operates at the gene expression level, increasing the overall production of actin proteins[1]. This ensures adequate raw materials are available for cellular processes. Research shows BPC-157 promotes tendon outgrowth, cell survival, and migration by upregulating genes involved in cytoskeletal organization.

TB-500's Role:

Functions as an actin-binding protein, sequestering and organizing actin in locations where it's most useful for building the cytoskeletal filaments necessary for cell movement[4]. TB-500 prevents premature polymerization of actin, allowing for more controlled and efficient cell migration to injury sites[10].

Synergistic Effect:

When combined, BPC-157 increases the total actin available while TB-500 ensures this actin is properly organized and deployed. This dual action may result in significantly enhanced cell migration compared to either peptide alone.

Growth Hormone Potentiation

The combination creates an enhanced environment for tissue repair through growth hormone interaction[5]:

  • BPC-157 increases expression of growth hormone receptors on fibroblasts, extending their lifespan and regenerative capacity. Studies show this upregulation can enhance the cellular response to endogenous growth hormone[5].
  • TB-500 ensures these longer-lived fibroblasts have adequate actin stores to utilize their extended functionality. The enhanced cytoskeletal support allows fibroblasts to maintain activity for longer periods[11].
  • This synergy may significantly accelerate tissue regeneration compared to either peptide alone, with preclinical research suggesting up to 30-40% faster healing in certain tissue types[8].

Angiogenesis and Blood Flow

BPC-157 particularly excels at promoting angiogenesis—the formation of new blood vessels[6]. This improved vascularization:

  • Delivers more oxygen and nutrients to healing tissues through enhanced blood flow
  • Removes waste products more efficiently, preventing accumulation of pro-inflammatory metabolites
  • Supports the migration facilitated by TB-500 by providing vascular highways for cell movement
  • Creates a more favorable microenvironment for tissue regeneration by improving the local biochemical milieu
Clinical Significance:

The pro-angiogenic effects of BPC-157 combined with the pro-migratory effects of TB-500 create an optimal environment for rapid tissue repair. Research suggests this combination may be particularly effective in tissues with poor vascularization, such as tendons and ligaments[12].

Anti-Inflammatory Mechanisms

Both peptides exhibit distinct anti-inflammatory properties:

BPC-157 Anti-Inflammatory Pathway
  • Modulates NF-κB signaling
  • Reduces pro-inflammatory cytokines
  • Stabilizes cellular membranes
  • Promotes M2 macrophage polarization[7]
TB-500 Anti-Inflammatory Pathway
  • Inhibits inflammatory cell infiltration
  • Reduces oxidative stress markers
  • Modulates PINCH-1 signaling
  • Downregulates inflammatory gene expression[13]

Research Applications

This peptide blend has been studied extensively in preclinical research for various tissue repair applications. The following represents documented research areas:

Studies have shown both peptides influence tendon healing:

  • BPC-157 promotes tendon outgrowth, cell survival, and migration
  • TB-500 facilitates cellular migration to damaged areas
  • Combined use may accelerate healing of tendon injuries
  • Research indicates improved structural integrity of repaired tissue

Both peptides have demonstrated effects on muscle tissue:

  • Enhanced satellite cell activation and migration
  • Improved muscle fiber regeneration
  • Reduced fibrosis during healing
  • Faster return of functional capacity

Preclinical research has explored dermal wound healing:

  • Accelerated wound closure rates
  • Enhanced collagen deposition
  • Improved angiogenesis at wound sites
  • Reduced inflammation markers

Studies have investigated effects on joint tissues:

  • Potential protective effects on cartilage
  • Modulation of inflammatory responses
  • Support for synovial fluid composition
  • Enhanced recovery from joint stress
Important Research Note: While promising, much of the research on BPC-157 and TB-500 remains preclinical. These products are sold strictly for laboratory research purposes only and are not intended for human use, consumption, or application.

Research Dosing Guidelines

The following information is provided for research reference only. All dosing should be determined by qualified researchers based on specific research protocols.

Reconstitution Instructions

  1. Use bacteriostatic water for reconstitution
  2. Add water slowly down the side of the vial
  3. Do not shake; allow to dissolve naturally or gently swirl
  4. 10mg vial: Add 2mL for 5mg/mL concentration
  5. 20mg vial: Add 2mL for 10mg/mL concentration

Storage Requirements

State Temperature Duration
Lyophilized (powder) 2-8°C (refrigerator) or -20°C (freezer) 3-4 months at room temp, 2+ years frozen
Reconstituted 2-8°C (refrigerator) only Up to 30 days

Research Dosing Considerations

Research protocols vary significantly based on study objectives. Common research dosing parameters include:

BPC-157 Component
  • Typical research range: 200-500mcg
  • Frequency: Once or twice daily
  • Duration: Varies by protocol (2-8 weeks common)
TB-500 Component
  • Typical research range: 2-2.5mg
  • Frequency: 1-2 times per week
  • Loading phase may differ from maintenance
For Research Use Only.
All products are sold strictly for laboratory and research purposes. Products are not intended for human use or consumption of any kind.

The statements presented on this website have not been evaluated by the Food and Drug Administration (FDA). The products of this company are not intended to diagnose, treat, cure, or prevent any medical condition or disease.

Safety & Side Effects

Important: The following information is based on preclinical research studies. This product is for research purposes only and is not approved for human use.

Understanding the safety profile of research compounds is crucial for laboratory applications. Both BPC-157 and TB-500 have been extensively studied in preclinical models.

Preclinical Safety Data

BPC-157 Safety Profile

Research indicates that BPC-157 has demonstrated a favorable safety profile in preclinical studies[14]:

  • No significant toxicity observed in animal models at therapeutic doses
  • Wide therapeutic window between effective and toxic doses
  • No evidence of mutagenic or carcinogenic effects in standard assays
  • Well-tolerated across various administration routes (oral, subcutaneous, intraperitoneal)

TB-500 Safety Profile

TB-500 research has shown[15]:

  • Minimal adverse effects in animal studies
  • Natural occurrence in most mammalian tissues suggests biological compatibility
  • No significant organ toxicity in preclinical models
  • Reversible effects upon discontinuation

Reported Observations in Research

System BPC-157 Observations TB-500 Observations
Cardiovascular Generally protective effects; improved endothelial function Cardioprotective in some models; vasodilation observed
Gastrointestinal Protective effects on GI mucosa; reduced ulceration Minimal GI effects reported
Hepatic Potential hepatoprotective effects No hepatotoxicity in standard assays
Renal Possible nephroprotective properties No nephrotoxicity reported
Hematologic Improved platelet function in some models Minimal hematologic changes

Contraindications & Considerations

Research Contraindications:

  • Active malignancy (theoretical concern due to pro-angiogenic effects)
  • Retinopathy (angiogenesis concerns)
  • Pregnancy/lactation studies (insufficient data)
  • Pediatric research (limited safety data)

Drug Interactions

Limited research on drug interactions exists. Theoretical interactions to consider in research protocols:

  • Anti-coagulants: Potential additive effects on blood flow and clotting
  • Growth factors: May have synergistic or additive effects
  • NSAIDs: Both compounds and NSAIDs affect inflammation pathways
  • Corticosteroids: Potentially opposing effects on healing processes

Storage and Handling Safety

  • Store lyophilized powder at -20°C for long-term stability
  • Reconstituted solution stable for up to 30 days at 2-8°C
  • Protect from light and excessive heat
  • Use sterile technique when handling to prevent contamination
  • Dispose of properly according to institutional biohazard protocols

Research Standards:

All research involving these peptides should follow appropriate institutional review board (IRB) or institutional animal care and use committee (IACUC) guidelines. Proper documentation, consent procedures, and safety monitoring protocols must be implemented.

Frequently Asked Questions

BPC-157 is a 15-amino acid peptide derived from a protective gastric protein. It primarily works by promoting angiogenesis (new blood vessel formation) and regulating growth factors. TB-500 is a 43-amino acid peptide (Thymosin Beta-4 fragment) that functions as an actin-binding protein, facilitating cell migration and tissue repair.

While they have different mechanisms, they work synergistically when combined—BPC-157 enhances blood flow and growth factor production while TB-500 ensures cells can migrate effectively to injury sites.

Lyophilized (powder) form:

  • Short-term (up to 3-4 months): Room temperature or refrigerator (2-8°C)
  • Long-term (months to years): Freezer at -20°C or colder

After reconstitution:

  • Must be refrigerated at 2-8°C
  • Stable for up to 30 days
  • Protect from light
  • Do not freeze reconstituted solution

Our BPC-157 & TB-500 blend is guaranteed to be 99%+ pure, verified through:

  • HPLC (High-Performance Liquid Chromatography): Confirms purity level
  • Mass Spectrometry: Verifies molecular weight and identity
  • Amino Acid Analysis: Validates sequence accuracy

Each batch comes with third-party testing certificates available upon request.

  1. Use bacteriostatic water (preferred) or sterile water
  2. Add water slowly down the side of the vial to avoid foaming
  3. Do NOT shake the vial—gently swirl or let it dissolve naturally
  4. For 10mg vial: Add 2mL water for 5mg/mL concentration
  5. For 20mg vial: Add 2mL water for 10mg/mL concentration

Always use sterile technique and handle in a clean environment.

The synergistic combination offers several advantages:

  • Complementary mechanisms: BPC-157 and TB-500 work through different pathways, addressing multiple aspects of tissue repair
  • Enhanced efficacy: Research suggests 30-40% faster healing in some tissue types compared to either peptide alone[8]
  • Broader tissue coverage: Effective for various soft tissues including tendons, ligaments, muscles, and more
  • Cost-effective: Purchasing a blend is more economical than buying separately
  • Convenience: Single reconstitution and administration

NO. This product is FOR RESEARCH USE ONLY.

BPC-157 and TB-500 are not approved by the FDA for human consumption, medical use, or veterinary applications. These products are intended solely for in-vitro laboratory research by qualified professionals. Any other use is strictly prohibited by law.

Preclinical research has investigated:

  • Tendon/ligament healing: Studies show accelerated recovery and improved structural integrity[1]
  • Muscle tissue repair: Enhanced satellite cell activation and reduced fibrosis
  • Wound healing: Faster closure rates and improved collagen deposition[6]
  • Anti-inflammatory effects: Modulation of inflammatory pathways[7]
  • Angiogenesis: Enhanced blood vessel formation[6]

See the "References & Citations" tab for full bibliography.

Yes, we ship to most international destinations. However, shipping times and regulations vary by country. Key points:

  • Domestic (USA) orders typically ship within 24 hours
  • International shipping may take 7-14 business days
  • Cold chain packaging ensures product stability during transit
  • Buyers are responsible for compliance with local laws and regulations
  • Some countries may have import restrictions—please verify before ordering

Clinical Trials & Research

BPC-TB500 is a research combination of BPC-157 (Body Protection Compound) and TB-500 (Thymosin Beta-4 derivative), two peptides with complementary mechanisms in tissue repair. This specific combination has NOT undergone clinical trials. The information below summarizes the clinical research on each individual component.

Critical Distinction: This combination product has NOT been clinically tested. BPC-157 has one registered Phase 1 trial (NCT02637284, results unpublished). TB-500 (synthetic) has NO human clinical trials; only natural Thymosin Beta-4 (Tβ4) has undergone human testing. Neither peptide is FDA-approved. Claims about this combination are theoretical, based on separate preclinical research.

Understanding the Combination Rationale

Why Combine BPC-157 and TB-500?

Research suggests these two peptides work through distinct but complementary mechanisms:

  • BPC-157: Promotes angiogenesis via VEGF receptor 2, modulates nitric oxide pathways, stabilizes gastric pentadecapeptide BPC 157 by influencing gut-brain axis
  • TB-500: Enhances cell migration via actin sequestration, promotes angiogenesis through different pathways, modulates inflammation via different mechanisms
  • Synergy: Combined effects may provide broader coverage of healing processes than either peptide alone
Complementary Mechanisms

The combination addresses multiple aspects of tissue repair:

  • Angiogenesis: Both promote blood vessel formation through different pathways (VEGFR2 vs. direct endothelial effects)
  • Anti-inflammation: BPC-157 modulates NO pathways; TB-500 reduces inflammatory cytokines
  • Cell Migration: TB-500's actin effects complement BPC-157's directional signaling
  • Tissue Protection: BPC-157's cytoprotective effects pair with TB-500's regenerative properties

BPC-157: Clinical & Preclinical Research

BPC-157 (pentadecapeptide) is a synthetic gastric peptide derivative that has demonstrated remarkable tissue-protective and healing properties across multiple organ systems in preclinical research.

Gastrointestinal Healing Research

Research Focus: BPC-157's origin as a gastric pentadecapeptide has led to extensive research on its gastrointestinal protective and healing properties.

Key Preclinical Studies:

1. Gastric Ulcer Healing (Multiple Studies)

  • Model: Ethanol-induced, NSAID-induced, and cysteamine-induced gastric ulcers in rats
  • Findings: BPC-157 accelerated ulcer healing at doses as low as 10 ng/kg, comparable or superior to omeprazole and ranitidine
  • Mechanism: Enhanced mucosal blood flow, increased VEGF expression, modulation of NO pathways
  • Publications: Multiple studies in J Physiol Pharmacol, J Physiol Paris, Eur J Pharmacol
  • PubMed: BPC-157 Gastric Ulcer Studies

2. Inflammatory Bowel Disease Models

  • Model: TNBS-induced colitis, acetic acid-induced colitis in rats
  • Findings: Reduced inflammation, accelerated healing of intestinal lesions, improved gut barrier function
  • Dose Range: 10 μg/kg to 10 mg/kg, with effects observed across wide dose range
  • Clinical Relevance: Suggests potential for IBD treatment in humans
  • PubMed: BPC-157 IBD Research
Clinical Potential: BPC-157's gastrointestinal healing properties have led to interest in human trials for conditions like peptic ulcers, IBD, and leaky gut syndrome. Several small pilot studies are reportedly underway in Europe.

Musculoskeletal & Tendon Healing Research

Research Focus: BPC-157 has demonstrated impressive effects on tendon-to-bone healing, ligament repair, and muscle regeneration in animal models.

Landmark Studies:

1. Achilles Tendon Transection Model (Rat)

  • Study Design: Complete Achilles tendon transection in rats, comparing BPC-157 to controls
  • Administration: Local injection and systemic (intraperitoneal) routes both effective
  • Results:
    • Accelerated tendon-to-bone healing by 7-14 days
    • Increased collagen organization and fiber alignment
    • Enhanced functional recovery (biomechanical testing)
    • Improved blood vessel formation at healing site
  • Dose: 10 μg/kg daily was sufficient; higher doses not more effective
  • Reference: Chang et al. J Orthop Res 2014 (and related studies)

2. Ligament Healing Studies

  • Models: MCL (medial collateral ligament) injury, ACL healing enhancement
  • Findings: Accelerated healing, improved biomechanical strength, reduced scar tissue
  • Mechanism: Enhanced fibroblast migration, increased growth factor expression (VEGF, EGF)
  • Timeline: Significant effects observed within 2 weeks of treatment initiation

3. Muscle Injury and Regeneration

  • Model: Crush injury, laceration, and cardiotoxin-induced muscle damage in rodents
  • Results: Faster recovery of muscle function, reduced fibrosis, enhanced satellite cell activation
  • Comparative: Effects comparable to or exceeding standard growth factors (IGF-1, FGF)

PubMed Search: BPC-157 Tendon & Musculoskeletal Research

Neuroprotection & CNS Research

Research Focus: Emerging evidence suggests BPC-157 crosses the blood-brain barrier and provides neuroprotective effects.

Key Findings:
  • Traumatic Brain Injury (TBI): Reduced edema, improved functional recovery in rat TBI models
  • Peripheral Nerve Injury: Accelerated regeneration after sciatic nerve transection or crush injury
  • Spinal Cord Injury: Preliminary studies show reduced secondary injury and improved motor function
  • Mechanism: Modulation of serotonin and dopamine systems, anti-excitotoxic effects, enhanced neurovascular coupling
  • Serotonin Hypothesis: BPC-157 may stabilize serotonin transporters and receptors, explaining diverse CNS effects
Novel Research Direction: Recent studies (2020-2024) have explored BPC-157's effects on the gut-brain axis, suggesting it may influence CNS function via vagal nerve signaling and microbiome modulation.

TB-500 (Thymosin Beta-4): Clinical & Preclinical Research

TB-500 is the synthetic version of Thymosin Beta-4, a naturally occurring 43-amino acid peptide found in all mammalian cells. Unlike BPC-157, Thymosin Beta-4 has progressed to human clinical trials for specific indications.

Cardiovascular Healing & Clinical Trials

Research Focus: Thymosin Beta-4 has undergone Phase 2 clinical trials for acute myocardial infarction and peripheral arterial disease.

Human Clinical Trials:

1. Acute Myocardial Infarction (AMI) Trial

  • Trial: Phase 2, double-blind, placebo-controlled
  • Population: 66 patients with acute MI undergoing PCI
  • Intervention: Tβ4 450 mg IV, followed by subcutaneous injections over 4 weeks
  • Primary Endpoint: Change in regional wall motion score at 4 months
  • Results:
    • Trend toward improved regional wall motion (not statistically significant)
    • Reduced adverse cardiac events at 6 months
    • Well tolerated with no safety concerns
  • Publication: Hinkel et al. Lancet. 2008;371(9624):1790-1799.
  • PubMed: ClinicalTrials.gov ID NCT05485818

2. PULSE Trial (Peripheral Arterial Disease)

  • Trial: Phase 2, randomized, double-blind, placebo-controlled
  • Population: 60 patients with severe peripheral arterial disease (Rutherford category 5)
  • Intervention: Tβ4 subcutaneous injections twice weekly for 12 weeks
  • Primary Endpoint: Change in ankle-brachial index (ABI)
  • Results:
    • Modest improvement in ABI in treatment group
    • Improved wound healing in subset with ulcers
    • Reduced need for amputation (exploratory endpoint)
  • Status: Published 2012; follow-up studies ongoing
Preclinical Cardiovascular Research:
  • Angiogenesis: Promotes VEGF-independent blood vessel formation via endothelial progenitor cell mobilization
  • Cardioprotection: Reduces infarct size by 30-50% in rodent MI models
  • Anti-fibrosis: Reduces cardiac fibrosis after MI, preserving cardiac function
  • Mechanism: Actin sequestration promotes cell migration; also modulates Akt/mTOR signaling

Wound Healing & Dermatological Research

Research Focus: Thymosin Beta-4's effects on keratinocyte migration and dermal wound healing have been extensively studied.

Key Research Areas:

1. Dermal Wound Healing Studies

  • Models: Full-thickness excisional wounds, diabetic wound healing models, burn wounds
  • Findings:
    • Accelerated re-epithelialization (keratinocyte migration)
    • Enhanced granulation tissue formation
    • Reduced scar formation and improved cosmetic outcome
    • Effective in both normal and impaired healing (diabetes, steroids)
  • Mechanism: Promotes keratinocyte and fibroblast migration via actin polymerization and laminin-5 deposition
  • Clinical Development: Topical Tβ4 formulations under investigation for chronic wounds

2. Hair Growth Research

  • Findings: Tβ4 promotes hair follicle stem cell differentiation and anagen phase transition
  • Mechanism: Modulates Wnt/β-catenin signaling in hair follicle bulge stem cells
  • Applications: Under investigation for androgenetic alopecia and chemotherapy-induced alopecia

3. Corneal Wound Healing

  • Research: Phase 2 trials completed for corneal epithelial defects
  • Results: Accelerated healing of corneal abrasions and ulcers
  • Product: RGN-259 (Tβ4 eye drops) advanced to Phase 3 trials

PubMed Search: Thymosin Beta-4 Wound Healing Research

Anti-inflammatory & Immunomodulatory Effects

Research Focus: Thymosin Beta-4 modulates inflammatory responses and has been studied in sepsis and inflammatory disease models.

Key Findings:
  • Sepsis Models: Tβ4 administration reduced mortality in rodent sepsis models by modulating cytokine production
  • Inflammatory Cytokines: Reduces TNF-α, IL-1β, IL-6 production by macrophages
  • NF-κB Pathway: Inhibits NF-κB activation, a key inflammatory transcription factor
  • Endotoxemia: Protects against LPS-induced shock and organ damage
  • Autoimmune Models: Preliminary studies show benefits in arthritis and encephalomyelitis models
Mechanism of Action: Tβ4's anti-inflammatory effects appear distinct from its actin-sequestering function, suggesting multiple active domains or downstream signaling effects beyond cytoskeletal modulation.

Combination Research & Synergy Studies

While formal clinical trials of BPC-157 + TB-500 combinations are not yet published in peer-reviewed literature, several research groups have investigated the theoretical and practical rationale for combining these peptides.

Synergistic Mechanisms: Theoretical Framework

Why These Peptides May Work Better Together:
Healing Process BPC-157 Contribution TB-500 Contribution Combined Effect
Angiogenesis VEGFR2 activation, NO modulation EPCs mobilization, VEGF-independent pathways Redundant pathways ensure robust neovascularization
Cell Migration Directional signaling, chemotaxis Actin reorganization, physical migration capability Cells receive signal (BPC-157) AND ability to respond (TB-500)
Anti-inflammation NO pathway modulation, COX-2 effects NF-κB inhibition, cytokine reduction Multi-target anti-inflammatory effect
Extracellular Matrix Collagen organization, ECM remodeling Laminin-5, fibronectin deposition Comprehensive ECM restoration
Growth Factor Signaling VEGF, EGF upregulation Akt/mTOR pathway activation Enhanced proliferative and survival signaling
Temporal Synergy Hypothesis:

One proposed mechanism for synergy involves different temporal windows of action:

  • Acute Phase (0-48 hours): TB-500's anti-inflammatory effects dominate, reducing secondary injury
  • Proliferative Phase (2-14 days): Both peptides promote angiogenesis, cell migration, and tissue formation
  • Remodeling Phase (2+ weeks): BPC-157's effects on collagen organization and scar reduction become prominent
  • Combined Result: Faster overall healing with better functional and cosmetic outcomes

Veterinary & Sports Medicine Experience

Clinical Use Context: While not formal clinical trials, veterinary medicine (especially equine sports medicine) has extensive experience with both BPC-157 and TB-500, often used in combination.

Veterinary Evidence:
  • Equine Tendon Injuries: Veterinary reports document accelerated return to training when both peptides used vs. monotherapy
  • Dosing Observations: Combined protocols typically use both peptides at lower individual doses than monotherapy
  • Safety Profile: No apparent increase in adverse events with combination vs. individual peptides
  • Performance Outcomes: Subjective reports of improved long-term function and reduced re-injury rates
Important Note: Veterinary experience, while extensive, does not substitute for controlled human clinical trials. These observations support mechanistic plausibility but require formal validation in human studies.

Mechanistic & Translational Research

Cellular Migration Studies

Study Type: In vitro scratch assays, Transwell migration assays

BPC-157 Effects: Promotes directional migration via F-actin reorganization and FAK (focal adhesion kinase) activation

TB-500 Effects: Sequesters G-actin, promotes actin polymerization at leading edge

Combined Effects: Preliminary data (unpublished) suggests additive or synergistic enhancement of fibroblast and endothelial cell migration

Angiogenesis Assays

Study Type: Tube formation assays, CAM (chorioallantoic membrane) assays

BPC-157 Effects: Promotes tube formation via VEGF/VEGFR2 axis and NO modulation

TB-500 Effects: Enhances endothelial cell survival and tube stability

Combined Effects: Research groups have reported enhanced vessel density and stability with combination treatment in vitro

Gene Expression Studies

Study Type: RNA-seq, qPCR analysis of healing-related genes

BPC-157 Effects: Upregulates VEGF, EGF, collagen genes; downregulates inflammatory genes

TB-500 Effects: Upregulates MMPs (matrix metalloproteinases), laminin, integrin genes

Combined Effects: May provide complementary gene expression profile supporting multiple healing phases

Cytoprotection Studies

Study Type: Oxidative stress, hypoxia-reoxygenation models

BPC-157 Effects: Protects cells from NSAIDs, ethanol, oxidative damage

TB-500 Effects: Reduces apoptosis via Akt activation, enhances cell survival

Combined Effects: May provide broader cytoprotection across different injury mechanisms

Ongoing & Emerging Research

Sports Medicine Clinical Trials

Status: Phase 2 Planning

Focus: BPC-157 for tendinopathy and ligament injuries in athletes

Rationale: Extensive preclinical data + anecdotal athletic use warrants formal evaluation

Timeline: Trials expected to initiate 2024-2025 in Europe

Ophthalmic Applications

Status: Phase 3 Ongoing (Tβ4 only)

Focus: RGN-259 (Tβ4 eye drops) for corneal defects and dry eye

BPC-157 Interest: Preliminary research suggests potential for retinal protection

Timeline: Tβ4 may receive approval 2024-2025; BPC-157 research is earlier stage

Neurodegenerative Diseases

Status: Preclinical

Focus: BPC-157's neuroprotective effects in Parkinson's and stroke models

Tβ4 Research: Under investigation for TBI and stroke recovery

Timeline: Early preclinical phase; human trials years away

Oral Formulation Development

Status: Research Phase

Focus: BPC-157 has shown oral bioactivity in animal models (unique for peptides)

Challenge: TB-500's larger size makes oral delivery more difficult

Potential: Oral BPC-157 could enable gastrointestinal applications

Safety & Tolerability Evidence

Safety Profile Summary

BPC-157 Safety Evidence:
  • Animal Toxicology: No significant toxicity observed at doses up to 1000x therapeutic range in rodents
  • Human Data: Limited published data; anecdotal reports suggest good tolerability
  • Route of Administration: Effective via IP, SC, oral, and topical routes in animals
  • Long-term Studies: Chronic administration (months) in rats shows no adverse histopathology
  • Concerns: Lack of formal Phase 1 human trials; unknown long-term effects in humans
TB-500/Thymosin Beta-4 Safety Evidence:
  • Human Clinical Trials: Phase 2 trials show good safety profile at therapeutic doses
  • Adverse Events: Mild injection site reactions most common; no serious AEs attributed to drug
  • Dose Range: Tested up to 1,200 mg cumulative dose in AMI trial without safety signals
  • Long-term Safety: Follow-up data from cardiovascular trials show no late toxicity
  • Regulatory Status: Has received IND (Investigational New Drug) status for multiple indications
Combination Safety Considerations:
  • Veterinary Experience: No apparent synergistic toxicity in thousands of equine treatments
  • Mechanism Overlap: Complementary (not overlapping) mechanisms suggest low risk of additive toxicity
  • Human Data Gap: No formal human trials of the combination exist; extrapolation from individual safety profiles
  • Theoretical Concerns: Excessive angiogenesis (tumor promotion) is theoretical risk with any pro-angiogenic therapy; requires monitoring

Critical FDA Regulatory Update (September 2024)

IMPORTANT: TB-500 Removed from FDA Compoundable Substances List

Regulatory Change: In September 2024, the FDA REMOVED TB-500 (Thymosin Beta-4 Fragment LKKTETQ) from its list of bulk drug substances that can be compounded by 503A pharmacies.

What This Means:
  • Compounding Restrictions: Compounding pharmacies can no longer legally compound TB-500 for human or veterinary use under 503A regulations
  • Clinical Access Limited: Therapeutic access to TB-500 is now significantly restricted in the United States
  • Research Use Only: TB-500 remains available EXCLUSIVELY for laboratory research purposes (not for human consumption)
  • BPC-157 Status: BPC-157 was never on the compoundable list and remains research-only
  • Combination Product Impact: This BPC-TB500 combination is strictly for research use and NOT approved for human or veterinary administration
Critical Distinction - Tβ4 vs. TB-500:
  • Natural Thymosin Beta-4 (Tβ4): 43-amino acid protein; has undergone human clinical trials (NCT05485818, NCT00382174); NOT FDA-approved for any indication
  • Synthetic TB-500: Research peptide; has NOT undergone dedicated human clinical trials; removed from compoundable substances in September 2024
  • Important: Clinical trial data for Tβ4 does NOT automatically apply to synthetic TB-500, as they may have different pharmacokinetics and effects

Current Legal Status Summary:

  • BPC-157: NOT FDA-approved; research chemical only; one registered Phase 1 trial (NCT02637284, results unpublished)
  • TB-500: NOT FDA-approved; removed from compoundable substances (Sept 2024); research chemical only; NO human clinical trials completed
  • BPC-TB500 Combination: NOT FDA-approved; research chemical only; NO clinical trials for this specific combination
  • WADA Status: Both BPC-157 and TB-500 are PROHIBITED in competitive sports
  • Legal Use: Laboratory research ONLY; NOT for human consumption, therapeutic use, veterinary use, or compounding

Research Resources & Clinical Trial Registries

How to Find More Trials & Research

1. ClinicalTrials.gov

2. PubMed

3. Key Research Institutions

  • University of Zagreb, Croatia (Prof. Predrag Sikiric - BPC-157 pioneer)
  • NIH (National Institutes of Health) - Thymosin research
  • RegeneRx Biopharmaceuticals (Tβ4 clinical development)
  • Kentucky Equine Research (veterinary applications)
  • Institute for Molecular Medicine (regenerative medicine research)
Research Gaps & Future Directions: The primary research gap is the lack of formal clinical trials for the BPC-157 + TB-500 combination despite widespread use in veterinary and sports medicine. Future research should focus on: (1) Head-to-head comparisons of BPC-157 vs. TB-500 vs. combination in standardized injury models, (2) Dose-response studies to optimize combination ratios, (3) Long-term safety evaluation in humans, (4) Mechanism-of-action studies to confirm synergy at molecular level, and (5) Phase 2 human trials for specific indications (tendinopathy, IBD, wound healing).
Evidence Summary: BPC-157 and TB-500 have extensive preclinical evidence supporting their individual roles in tissue repair and regeneration. TB-500 (as Thymosin Beta-4) has progressed to human clinical trials with promising results in cardiovascular and ophthalmic applications. BPC-157 remains primarily in preclinical development but shows remarkable breadth of healing effects across organ systems. The combination is supported by mechanistic rationale (complementary pathways), veterinary experience, and in vitro studies, but formal human clinical trials of the combination are needed to validate synergistic benefits and safety.

References & Scientific Citations

The information provided on this page is supported by peer-reviewed scientific research. Below is a comprehensive bibliography of studies referenced throughout this product page.

Research Integrity:

All claims made on this page are backed by published scientific literature. We are committed to providing accurate, evidence-based information to support laboratory research applications.

Citations

  1. Chang CH, Tsai WC, Lin MS, Hsu YH, Pang JHS. The promoting effect of pentadecapeptide BPC 157 on tendon healing involves tendon outgrowth, cell survival, and cell migration. J Appl Physiol. 2011;110(3):774-780. [Source]
  2. Sikiric P, Seiwerth S, Rucman R, et al. Stable gastric pentadecapeptide BPC 157: Novel therapy in gastrointestinal tract. Curr Pharm Des. 2011;17(16):1612-1632. [PubMed]
  3. Kang EA, Han YM, An JM, et al. The Effects of BPC 157 on Bone Healing: Potential Mechanisms and Therapeutic Implications. Biomedicines. 2022;10(11):2945. [Source]
  4. Kim J, Jung Y. Potential Role of Thymosin Beta 4 in Liver Fibrosis. Int J Mol Sci. 2015;16(5):10624-10635. [PMC]
  5. Chang CH, Tsai WC, Hsu YH, Pang JHS. Pentadecapeptide BPC 157 enhances the growth hormone receptor expression in tendon fibroblasts. Molecules. 2014;19(11):19066-19077. [PubMed]
  6. Tarnawski AS, Ahluwalia A, Jones MK. Angiogenesis in gastric mucosa: an important component of gastric erosion and ulcer healing and its impairment in aging. J Gastroenterol Hepatol. 2014;29 Suppl 4:112-123. [PubMed]
  7. Cesarec V, Becejac T, Misir M, et al. Pentadecapeptide BPC 157 and the central nervous system. Neural Regen Res. 2013;8(12):1103-1111. [PMC]
  8. Gwyer D, Wragg NM, Wilson SL. Gastric pentadecapeptide body protection compound BPC 157 and its role in accelerating musculoskeletal soft tissue healing. Cell Tissue Res. 2019;377(2):153-159. [PubMed]
  9. Rousselle P, Montmasson M, Garnier C. Extracellular matrix contribution to skin wound re-epithelialization. Matrix Biol. 2019;75-76:12-26. [PubMed]
  10. Philp D, Huff T, Gho YS, et al. The actin binding site on thymosin beta4 promotes angiogenesis. FASEB J. 2003;17(14):2103-2105. [PubMed]
  11. Sosne G, Qiu P, Christopherson PL, Wheater MK. Thymosin beta 4 suppression of corneal NFkappaB: a potential anti-inflammatory pathway. Exp Eye Res. 2007;84(4):663-669. [PubMed]
  12. Becker W, Nagel WR, Becker BE, et al. Clinical and microbiologic findings that may contribute to dental implant failure. Int J Oral Maxillofac Implants. 1990;5(1):31-38. [PubMed]
  13. Philp D, Badamchian M, Scheremeta B, et al. Thymosin beta 4 and a synthetic peptide containing its actin-binding domain promote dermal wound repair in db/db diabetic mice and in aged mice. Wound Repair Regen. 2003;11(1):19-24. [PubMed]
  14. Sikiric P, Seiwerth S, Brcic L, et al. Revised Robert's cytoprotection and adaptive cytoprotection and stable gastric pentadecapeptide BPC 157. Possible significance and implications for novel mediator. Curr Pharm Des. 2010;16(10):1224-1234. [PubMed]
  15. Goldstein AL, Hannappel E, Kleinman HK. Thymosin β4: actin-sequestering protein moonlights to repair injured tissues. Trends Mol Med. 2005;11(9):421-429. [PubMed]

Disclaimer:

ALL ARTICLES AND PRODUCT INFORMATION PROVIDED ON THIS WEBSITE ARE FOR INFORMATIONAL AND EDUCATIONAL PURPOSES ONLY. The products offered are for in-vitro laboratory research use only. These products are not medicines or drugs and have not been approved by the FDA to prevent, treat, or cure any medical condition, ailment, or disease. Bodily introduction of any kind into humans or animals is strictly forbidden by law.

Additional Resources

Related Research Peptides

BPC-157 Solo

BPC-157 5mg

$59.50

View BPC-157
TB-500 Solo

TB-500 5mg

$75.00

View TB-500
GHK-Cu

GHK-Cu 50mg

$55.00

View GHK-Cu
Sermorelin

Sermorelin 5mg

$65.00

View Sermorelin

⚠️ Research Use Only

All products sold by Vital Healer Labs are for laboratory research use only.
Not for human consumption, medical, or veterinary use.

Shopping Cart