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Tissue & repair research · RESEARCH PROFILE

TB-500

A thymosin-related research label with important sequence differences.

2 specifications·13 source documents·Source updated Jun 14, 2026

At a glance

A thymosin-related research label with important sequence differences.

This profile separates the compound’s scientific background from specification-specific preparation and source schedules. Begin with the research findings and limitations, then select the formulation you want to examine.

How it works

The TB-500 name is used in discussions of thymosin beta-4 and peptide fragments. Full-length thymosin beta-4 and an isolated fragment should not be assumed to have identical activity or evidence.[1][2][5]

Potential benefits & side effects

Interpret each outcome in the context of the study population, formulation and evidence type. Research findings do not establish a personal treatment outcome.

Potential benefits & research findings

Repair and cell-migration findings should be checked against the exact sequence studied. Evidence from topical, animal or veterinary settings does not validate a systemic human regimen.[5][1][5]

Read the original publications to see the measured endpoints, comparator, duration and uncertainty. Mechanistic plausibility and a favorable experimental result are different from demonstrated clinical benefit.

Side effects & evidence limitations

Interpret the reported adverse effects together with the study population, route and observation period. Small or short studies can miss uncommon and delayed harms. Evidence from a related compound does not establish the safety of TB-500.

Source-reported adverse effects and cautions

  • Generally well tolerated in veterinary studies; occasional mild injection‑site reactions (redness, tenderness) reported.
  • Human safety data is limited; no large‑scale clinical trials have been completed for TB‑500 specifically[11].
  • Sources are available for independent reading. Individual claims and research schedules have not yet undergone an independent clinical review by Pep Science.

    Editorial responsibility
    Pep Science editorial desk
    Last independent review
    Not yet recorded
    Editorial standards & corrections

    SPECIFICATIONS & SOURCE SCHEDULES

    Explore a vial size

    Select the exact formulation. Vial content, target dose and prepared concentration are different measurements.

    Showing 10 mg · 1 source tables

    Source-derived research information. Table phases retain the source’s actual duration; open-ended phases are not converted into a fixed eight-week course. Review the original study before interpreting a schedule.

    Standard / Gradual Approach (3 mL = ~3.33 mg/mL)

    Weeks 1–2Weeks 3–4Weeks 5–8Weeks 9–12
    PhaseDaily Dose (mcg)Units (per injection) (mL)
    Weeks 1–2500 mcg15 units (0.15 mL)
    Weeks 3–4600 mcg18 units (0.18 mL)
    Weeks 5–8750 mcg23 units (0.23 mL)
    Weeks 9–121000 mcg30 units (0.30 mL)

    Frequency: Inject once daily subcutaneously. This schedule uses the largest practical dilution (3.0 mL) to keep per‑injection units in a comfortable range for accurate measurement. Total weekly dose averages ~5 mg, consistent with research protocols[3][4].

    Additional schedule context & duration

    Concise summary of the once‑daily regimen.

    • Goal: Support tissue repair, wound healing, and angiogenesis through the active thymosin beta‑4 fragment mechanism[5][1].
    • Schedule: Daily subcutaneous injections for 8–12 weeks (extend to 16 weeks if research goals require).
    • Dose Range: 500–1000 mcg daily with gradual titration (~5 mg/week average).
    • Reconstitution: 3.0 mL per 10 mg vial (~3.33 mg/mL) for accurate unit measurements.
    • Storage: Lyophilized frozen; reconstituted refrigerated; avoid freeze–thaw cycles of reconstituted solution.

    Suggested daily titration approach.

    • Start: 500 mcg daily; increase by ~100–150 mcg every 2 weeks as tolerated.
    • Target: 750–1000 mcg daily by Weeks 5–12.
    • Frequency: Once per day (subcutaneous).
    • Cycle Length: 8–12 weeks; optional extension to 16 weeks based on research protocol.
    • Timing: Any consistent time daily; rotate injection sites systematically.

    Read this source protocol ↗ · View cited documents ↓

    Preparation

    Preparation and stability depend on the formulation, diluent, container and handling. The source-specific notes below apply to the selected record.
    Reconstitution Steps
    1. Draw 3.0 mL bacteriostatic water with a sterile syringe.
    2. Inject slowly down the vial wall; avoid foaming.
    3. Gently swirl/roll until dissolved (do not shake).
    4. Label with date and concentration; refrigerate at 2–8 °C (35.6–46.4 °F), protected from light.

    Important: This guide is for educational purposes only and is not medical advice. TB‑500 is not FDA‑approved for human use and is for research purposes only.

    Storage Instructions

    Proper storage preserves peptide quality and activity.

    • Lyophilized: Store at −20 °C (−4 °F) in dry, dark conditions; minimize moisture exposure[6].
    • Reconstituted: Refrigerate at 2–8 °C (35.6–46.4 °F); do not freeze reconstituted solution as freezing can denature peptides.
    • Allow vials to reach room temperature before opening to reduce condensation uptake.
    • Use reconstituted vials within 28 days when stored with bacteriostatic water preservative[7].

    Injection Technique

    General subcutaneous guidance from clinical best‑practice resources[12][13].

    • Clean the vial stopper and skin with alcohol; allow to air dry completely.
    • Pinch a skinfold at the injection site; insert the needle at 45–90° into subcutaneous tissue[12].
    • Do not aspirate for subcutaneous injections; inject slowly and steadily[12].
    • Rotate sites systematically within approved areas (abdomen, thighs, upper arms) to avoid lipohypertrophy[8].
    • Wait 5–10 seconds after injection before withdrawing needle to prevent medication leakage.

    Materials & quantity planning

    Source materials checklist · 10 mg

    Plan based on an 8–16 week daily protocol with gradual titration.

    • Peptide Vials (TB‑500, 10 mg each):

      • 8 weeks ≈ 4 vials
      • 12 weeks ≈ 7 vials
      • 16 weeks ≈ 10 vials
    • Insulin Syringes (U‑100):

      • Per week: 7 syringes (1/day)
      • 8 weeks: 56 syringes
      • 12 weeks: 84 syringes
      • 16 weeks: 112 syringes
    • Bacteriostatic Water (10 mL bottles): Use ~3.0 mL per vial for reconstitution.

      • 8 weeks (4 vials): 12 mL2 × 10 mL bottles
      • 12 weeks (7 vials): 21 mL3 × 10 mL bottles
      • 16 weeks (10 vials): 30 mL3 × 10 mL bottles
    • Alcohol Swabs: One for the vial stopper + one for the injection site each day.

      • Per week: 14 swabs (2/day)
      • 8 weeks: 112 swabs → recommend 2 × 100‑count boxes
      • 12 weeks: 168 swabs → recommend 2 × 100‑count boxes
      • 16 weeks: 224 swabs → recommend 3 × 100‑count boxes


    Calculate a phased quantity

    Enter each finite phase from the schedule you are studying. Open-ended phases need an explicit duration. Calculation uses 10 mg per vial and 3 mL per vial.

    Complete each phase to calculate totals.

    Quantity estimates exclude preparation losses and expiry. Follow the formulation’s handling and disposal requirements.

    FOLLOW THE EVIDENCE

    References & further reading

    Original publications and source documents cited across this product’s variants. A listed source is not an independent endorsement of a dosing schedule.

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    Related topics are not interchangeable compounds or formulations.