For informational and research purposes only. Not medical advice. Content is aggregated from public sources. Always consult a qualified healthcare provider.
Healing & Recovery · Comparison

LL-37 vs TB-500

A neutral, side-by-side comparison of two healing & recovery peptides — their mechanisms, dosing ranges, administration routes, side effects, and research evidence. For research and educational purposes only.

LL-37TB-500
CategoryHealing & RecoveryHealing & Recovery
Also known asCathelicidin LL-37, hCAP-18 C-terminal fragment, CRAMP (murine equivalent)Thymosin Beta-4, Tβ4, TB500
EvidenceResearch-stagePreclinical only
Dosing range100mcg–500mcg mcg, Daily or 3–5x weekly2mg–10mg mg, twice weekly (loading), weekly (maintenance)
AdministrationSubcutaneous injection, Intranasal (for respiratory applications), Topical (wound care)Subcutaneous injection, Intramuscular injection
Key side effectsInjection site redness and irritation (common — pro-inflammatory at injection site), Transient flu-like symptoms (immune activation), Local induration, High doses may be cytotoxic — dose-response curve is non-linearHead rush / lightheadedness (transient), Lethargy at higher doses, Injection site discomfort, Nausea (rare)
Cited sources3 references2 references

Key differences

  • Evidence level differs: LL-37 is research-stage, while TB-500 is preclinical only.
  • Administration: LL-37 — Subcutaneous injection, Intranasal (for respiratory applications), Topical (wound care); TB-500 — Subcutaneous injection, Intramuscular injection.
  • Dosing units differ: LL-37 is dosed in mcg, TB-500 in mg — they operate at different scales.
  • Frequency: LL-37 is typically Daily or 3–5x weekly; TB-500 is twice weekly (loading), weekly (maintenance).
  • Research depth: this profile cites 3 sources for LL-37 vs 2 for TB-500.

How each works

LL-37

LL-37 exerts antimicrobial activity by disrupting bacterial membranes via electrostatic interaction with negatively charged lipopolysaccharide — effective against gram-positive and gram-negative bacteria, fungi, and enveloped viruses including SARS-CoV-2 in vitro. Beyond direct antimicrobial action, LL-37 modulates innate immunity through TLR4 signaling, promotes wound healing via EGFR and FPRL1 receptor activation, and has demonstrated anti-biofilm activity against P. aeruginosa and S. aureus. Vitamin D is the primary driver of endogenous LL-37 production.

TB-500

TB-500 promotes healing by upregulating actin, which drives cell migration to injury sites. Animal studies show accelerated repair of muscle tears, tendon injuries, and corneal wounds. It also demonstrates anti-inflammatory properties and has been studied for cardiac tissue repair following ischemic injury.

Read the full LL-37 profileRead the full TB-500 profile

This comparison aggregates public research and structured profile data for informational purposes only. It is not medical advice and does not recommend either compound for human use. Consult a qualified healthcare provider before considering any peptide.