LL-37
Human cathelicidin antimicrobial peptide. Endogenous component of innate immunity with broad-spectrum antimicrobial, immunomodulatory, and wound-healing activity. Researched as a topical and systemic therapeutic across multiple indications; no FDA-approved formulation yet.
Educational only — not medical advice. SmartPeptide does not prescribe, diagnose, or treat. Always consult a licensed healthcare provider before using any peptide, supplement, medication, or protocol.
What the research shows
Robust in-vitro and animal-model evidence for antimicrobial activity (including biofilm disruption), wound healing acceleration, and immunomodulation. Small human topical trials suggest promise for chronic wounds. No approved systemic indication.
What's still experimental
Most therapeutic applications. Optimal route, dose, formulation, and safety profile in systemic use are unknown.
Anecdotal / community reports
Community use for chronic infections, Lyme disease, biofilm-related conditions. These uses are not supported by published RCTs and may risk LL-37's known pro-inflammatory effects in susceptible individuals.
Anecdotal reports are NOT scientific evidence. They reflect personal experience and may not generalize.
FDA approval status
Source: openFDA + DailyMed (NIH/NLM)Doses studied in research
Source: Published clinical trialWhat published trials tested or FDA-approved labels specify. Reporting research facts — not a SmartPeptide recommendation.
LL-37 has documented pro-inflammatory effects in autoimmune contexts (psoriasis, lupus). Anyone with autoimmune disease should specifically discuss this with a rheumatology-informed clinician before considering.
The doses below are aggregated from research-peptide community forums (Reddit, biohacker discussions). They are NOT supported by clinical trials, NOT FDA-approved, and NOT a SmartPeptide recommendation. Source purity, dose accuracy, and user-reported outcomes are unverifiable. We display this only because the information is publicly available elsewhere — visitors should absolutely consult a licensed clinician familiar with experimental peptides before any use.
Notes from the source: LL-37 can be pro-inflammatory in certain contexts (psoriasis, lupus). Systemic safety data in humans is sparse.
How clinicians typically protocol this
Third-party reference · not our recommendationDosing phases, cycle lengths, and administration timing as listed in a compounding-pharmacy clinician reference guide. Shown so you can see what a real protocol looks like — and bring informed questions to a licensed clinician.
Dose numbers, frequencies, and cycle lengths in this panel are extracted from a clinician-facing reference protocol distributed by a US-based compounding pharmacy in November 2025. SmartPeptide has paraphrased all descriptive text and adds no endorsement. Always consult a licensed clinician.
LL-37 has been implicated in autoimmune pathology (psoriasis, lupus flares). Avoid in known autoimmune disease unless a clinician directs otherwise.
Only known human cathelicidin peptide; antimicrobial and immunomodulatory.
Protocol phases
in a carrier solution/gel
Protocol notes: The reference suggests hydration, sleep, and possibly co-administering BPC-157 or KPV to buffer inflammatory response.
FDA enforcement & recalls
Live · openFDA Drug Enforcement API- Class IITerminated· Voluntary: Firm initiatedFDA record
LL-37 2 mg/mL (5 mL) Injection, 5 mL vials, Rx only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081 USA
Reason: Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
Apr 5, 2022·North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding - Class IIOngoing· Voluntary: Firm initiatedFDA record
LL-37, 2000 MCG/ML, 2 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN
Reason: Lack of Assurance of Sterility: due to concerns with production processes which cannot assure sterility of products intended to be sterile.
Nov 30, 2020·Advanced Nutriceuticals, LLC
Mechanism & targets
ChEMBL · UniProt · Open TargetsMolecule (ChEMBL)
View on ChEMBLProtein targets (UniProt)
- Cathelicidin antimicrobial peptideP49913gene: CAMPHomo sapiens· 170 aaReviewed
Antimicrobial protein that is an integral component of the innate immune system (PubMed:14978112, PubMed:16637646, PubMed:18818205, PubMed:22879591, PubMed:9736536). Binds to bacterial lipopolysaccharides (LPS) (PubMed:16637646, PubMed:18818205). Acts via neutrophil N-formyl peptide receptors to enhance the release of CXCL2 (PubMed:22879591). Postsecretory processing generates multiple cathelicidin antimicrobial peptides with various lengths which act as a topical antimicrobial defense in sweat…
- Cathelicidin antimicrobial peptideQ1KLX2gene: CAMPPongo pygmaeus· 170 aaReviewed
Antimicrobial protein that is an integral component of the innate immune system (By similarity). Binds to bacterial lipopolysaccharides (LPS) (By similarity). Acts via neutrophil N-formyl peptide receptors to enhance the release of CXCL2 (By similarity). Postsecretory processing generates multiple cathelicidin antimicrobial peptides with various lengths which act as a topical antimicrobial defense in sweat on skin (By similarity). The unprocessed precursor form, cathelicidin antimicrobial peptid…
- Cathelicidin antimicrobial peptideQ1KLX7gene: CAMPMacaca fascicularis· 170 aaReviewed
Antimicrobial protein that is an integral component of the innate immune system (By similarity). Binds to bacterial lipopolysaccharides (LPS) (By similarity). Acts via neutrophil N-formyl peptide receptors to enhance the release of CXCL2 (By similarity). Postsecretory processing generates multiple cathelicidin antimicrobial peptides with various lengths which act as a topical antimicrobial defense in sweat on skin (By similarity). The unprocessed precursor form, cathelicidin antimicrobial peptid…
Live research
PubMed · ClinicalTrials.gov · Europe PMC · OpenAlexClinical trials (ClinicalTrials.gov)
- Impact of Vitamin D Supplementation on Severity of Pediatric Atopic DermatitisCOMPLETEDNCT01996423 · NA · n=101 · 2014-04
- Rapid Normalization of Vitamin D Deficiency in PICUCOMPLETEDNCT03742505 · PHASE3 · n=424 · 2019-06-17
- Fermented Milk on the Appearance of Common Winter Infectious DiseasesCOMPLETEDNCT02367612 · PHASE2 · n=140 · 2014-12
- Assessment of Vitamin D Supplementation and Immune FunctionCOMPLETEDNCT01399151 · NA · n=23 · 2011-01
- To Investigate the Effects of Bifidobacterium Animalis Subsp. Lactis XLTG11 on Growth and Development, Incidence of Allergy and Immune Function in InfantsRECRUITINGNCT07490587 · PHASE2 · n=366 · 2024-01-01
Europe PMC — 193,097 additional records
Includes EU/UK studies and PubMed Central full-text articles. Often surfaces research weeks before PubMed indexes it.
- Eradicating <i>Helicobacter pylori</i> and reversing precancerous intestinal metaplasia by gastric epithelial cells-localizable oral nanomedicinesMa S, Zhang Z, Hao J, et al. · 2026
- LncRNA6470/ace-miR-750-y axis modulates <i>AcPP2A</i> gene, immune response and survival of eastern honey bee larvae during fungal infectionFan X, Zhang K, Yang Y, et al. · 2026
- Changes in nurses' quality of work life prior to and during COVID: A repeated cross-sectional analysisHipel I, Keefe J, Duynisveld A, et al. · 2026Open access
- Fibrinogen-like protein 2-complement C3 interaction exacerbates tubular inflammation in acute kidney injury by elevating complement C3a levelsWan W, Yang Q, Li J, et al. · 2026Open access
Research volume (OpenAlex topic graph)
Human clinical evidence
Semantic Scholar · AI TLDRs · influence-rankedHuman-study summaries for “LL-37 OR cathelicidin LL-37” are available on Semantic Scholar but the shared free-tier API quota is exhausted right now. Try refreshing in a few minutes, or check the PubMed and Europe PMC panels above for the same literature.
Research funding & verification
NIH RePORTER · CrossRef DOI registryNIH-funded research
U.S. National Institutes of Health- 5R44DK069924-07$1.9MClinical Trial of Antimicrobial Skin to treat Diabetic UlcersAllen R. Comer · STRATATECH CORPORATION · FY2012
- 1ZIAES103328-03$1.6MMechanisms of transcriptional and replicative mutagenesisPaul Doetsch · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · FY2020
- 1ZIAES103328-04$1.3MMechanisms of transcriptional and replicative mutagenesisPaul Doetsch · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · FY2021
- 1ZIAES103328-02$1.3MMechanisms of transcriptional and replicative mutagenesisPaul Doetsch · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · FY2019
Publication landscape
CrossRef · DOI registry- National Natural Science Foundation of China31,094 works
- National Science Foundation4,181 works
- National Key Research and Development Program of China4,007 works
- National Institutes of Health3,706 works
- Fundamental Research Funds for the Central Universities3,134 works
- National Research Foundation of Korea2,597 works
Funder diversity is a credibility signal. Research concentrated in a single drug company's funding warrants more scrutiny than research funded across NIH, charities, and academic grants.
Preprints — cutting edge
bioRxiv · medRxiv · via Europe PMCPreprints have NOT been peer-reviewed. They are early research shared by authors before formal validation. Treat findings as preliminary.
- PreprintCoarse composition suffices: tabular in-context learning for multi-activity antimicrobial peptide profilingKumar R, Pal A, Solanki D, et al. · 2026-08-28
- PreprintLoss of endothelial cell FAK represses cisplatin-induced vascular senescence in distal niches to reduce lung metastatic burdenBenguigui M, Lockwood A, Rajendram R, et al. · 2026-08-25
- PreprintEffect of transitioning virally suppressed children and adolescents with HIV to dolutegravir-based antiretroviral therapy: emulated target trials in a large cohort in South AfricaBrown JA, Sookrajh Y, Mtila L, et al. · 2026-08-22
- PreprintAn audit assessing data quality, viral suppression, and transition to dolutegravir among children and adolescents with HIV in care at eThekwini Municipality, South AfricaHlabisa M, Mtila L, Lushaba N, et al. · 2026-08-21
- PreprintEffects of Endogenous and Exogenous LL37 on the Proliferation, Migration, and Osteogenic Differentiation of BMSCs and the PI3K/Akt Signaling Pathway in OsteogenesisZhu Y, Qin K, Zhang G, et al. · 2026-08-20
- PreprintValorisation of invasive North Sea macroalgae as functional feed additives to improve disease resilience in Pacific white shrimp (Litopenaeus vannamei)Irawan FP, Gómez NG, Vermeylen V, et al. · 2026-08-20
Known risks
Cytotoxicity at high concentrations (LL-37 can be toxic to human cells, not just bacteria). Pro-inflammatory effects in certain contexts (psoriasis, lupus). Limited human pharmacokinetic data.
Reported side effects
Topical: skin irritation. Systemic: poorly characterized in humans. Theoretical immune-modulation concerns.
FDA adverse event reports (FAERS)
Updated quarterly by FDAWhat requires medical supervision
Not FDA-approved. Should only be considered under a clinician familiar with antimicrobial peptide research.
Questions for your clinician
- Is there published human evidence for my specific indication?
- What's the risk of immune dysregulation in my case?
- Are there FDA-approved alternatives we should try first?