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Peptide Database

Goals
Fat LossMuscle BuildingInjury HealingAnti-AgingCognitive EnhancementSleep OptimizationImmune SupportGut HealingSkin RejuvenationSexual Health
Peptides
Adipotide
Weight Management
AOD-9604
Weight Management
BPC-157
Healing & Recovery
Cagrilintide
Weight Management
CJC-1295
Growth Hormone
DSIP
Sleep & Recovery
Epithalon
Anti-Aging
GHK-Cu
Anti-Aging
GHRP-2
Growth Hormone
HCG
Hormone Support
Hexarelin
Growth Hormone
HGH
Growth Hormone
IGF-1 LR3
Growth Hormone
Kisspeptin
Hormone Support
Melanotan-2
Cosmetic
MOTS-C
Metabolic
NAD+
Anti-Aging
Oxytocin Acetate
Hormone Support
PEG-MGF
Recovery
PNC-27
Cancer Research
PT-141
Sexual Health
Retatrutide
Weight Management
Selank
Cognitive
Semaglutide
Weight Management
Semax
Cognitive
Sermorelin
Growth Hormone
Snap-8
Cosmetic
SS-31
Mitochondrial
TB-500
Healing & Recovery
Tesamorelin
Growth Hormone
Thymosin Alpha-1
Immune
Tirzepatide
Weight Management
Total Peptides: 32
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Peptide Comparison

PidotimodvsLL-37

Synthetic dipeptide immunomodulator that enhances both innate and adaptive immunity through Toll-like receptor activation

Human cathelicidin-derived antimicrobial peptide (37 amino acids) that disrupts bacterial membranes at MIC 0.62 μM against S. aureus, neutralizes endotoxin (LPS) to prevent septic shock, and has reached Phase II clinical trials as Ropocamptide for wound healing — achieving 6-fold accelerated healing at 0.5 mg/mL in venous leg ulcers

ImmuneImmune

At a Glance

Quick
comparison

Dose Range

Pidotimod

400–800 mg

LL-37

0.5–1.6 mg/mL (topical)

Frequency

Pidotimod

Multiple times daily

LL-37

Once daily

Administration

Pidotimod

Oral (tablet)

LL-37

Topical application (wound healing)

Cycle Length

Pidotimod

12+ weeks

LL-37

12+ weeks

Onset Speed

Pidotimod

Moderate (1-2 weeks)

LL-37

Moderate (1-2 weeks)

Evidence Level

Pidotimod

Moderate human trials (Phase 1-2)

LL-37

Moderate human trials (Phase 1-2)

Efficacy

Benefit
ratings

Pidotimod
LL-37

Immune

Pidotimod95%
LL-3785%

Healing & Recovery

Pidotimod65%
LL-370%

Anti-Aging

Pidotimod45%
LL-370%

Healing

Pidotimod0%
LL-3792%

Technical Data

Compound
specifications

Pidotimod

Molecular Formula

C9H12N2O4S

Molecular Weight

244.27 g/mol

Half-Life

Approximately 4 hours

Bioavailability

~45% (oral)

CAS Number

121808-62-6

LL-37

Molecular Formula

C205H340N60O53

Molecular Weight

4,493.26 Da

Half-Life

Short systemic half-life (minutes) due to protease susceptibility; local tissue persistence at wound sites is longer due to binding to extracellular matrix components and lipid membranes

Bioavailability

Topical application achieves high local wound-bed concentrations; systemic bioavailability limited by rapid proteolytic degradation and serum protein binding; not intended for oral delivery

CAS Number

154947-66-7

Protocols

Dosing
tiers

Pidotimod

starting

400 mg twice daily (acute) / 400 mg once daily (prevention)

Once to twice daily

15 days acute treatment, then 60 days maintenance

Available as oral solution, sachets, or tablets. Best taken on an empty stomach (30 minutes before meals) for optimal absorption. Standard pediatric course is 15 days during acute infection followed by 60 days of once-daily prevention.

standard

800 mg twice daily (acute) / 800 mg once daily (prevention)

Once to twice daily

15 days acute treatment, then 60 days maintenance

Take on an empty stomach for best absorption. During acute infection, use 800 mg twice daily for 15 days. For prevention of recurrent infections, continue with 800 mg once daily for up to 60 days. Tablets and sachets are the most common adult formulations.

advanced

800 mg once to twice daily

Once to twice daily

60-90 days continuous

Extended courses may be considered for immunocompromised patients including those with HIV, elderly patients with frequent pneumonia, or patients with chronic respiratory conditions. Clinical studies in HIV patients used 800 mg twice daily for 4 weeks with sustained immune benefits for at least 4 weeks post-treatment.

LL-37

starting

0.5 mg/mL topical application

Once daily or every other day

2-4 weeks initial assessment

Apply LL-37 solution directly to wound bed after gentle cleansing. Cover with appropriate wound dressing. This concentration demonstrated the strongest efficacy in Phase I/IIa clinical trials for venous leg ulcers, with a 6-fold healing rate increase over placebo. Begin with every-other-day application to assess local tolerability before advancing to daily use.

standard

0.8 mg/mL topical application

Once daily

4-8 weeks

Standard clinical protocol based on Phase I/IIa dose-finding results. Apply to wound bed daily after cleansing, using sterile application technique. The peptide provides both antimicrobial clearance of wound bioburden and pro-healing effects through FPRL1-mediated angiogenesis and keratinocyte migration. Monitor wound healing progression weekly with photographic documentation.

advanced

1.6 mg/mL topical application

Once daily

8-12 weeks

Highest concentration tested in Phase I/IIa trials. Well-tolerated with no serious adverse events at this dose. Reserved for refractory wounds that have not responded to lower concentrations. The higher concentration provides enhanced antimicrobial activity and anti-biofilm effect for heavily colonized or biofilm-associated wounds. Clinical supervision recommended for extended treatment courses.

Applications

Best
suited for

Pidotimod

Recurrent Respiratory Infections

Pidotimod is specifically indicated and most widely studied for preventing recurrent respiratory tract infections (RRTIs), particularly in children over 3 years. Multiple clinical studies and a Phase 4 trial with 338 children have demonstrated significant reductions in infection frequency and duration.

Immunocompromised Patients

Patients with documented cell-mediated immunodepression, including those with HIV or the elderly with weakened immune function, may benefit from pidotimod's ability to enhance T-cell function and rebalance cytokine production.

Seasonal Immune Support

Preventive courses before cold and flu season can strengthen immune defenses through TLR activation and enhanced mucosal immunity (increased salivary IgA), reducing susceptibility to viral respiratory infections.

Chronic Respiratory Conditions

Patients with chronic bronchitis, bronchiectasis, or COPD who experience frequent exacerbations may benefit from pidotimod as an adjunctive therapy to reduce infection-triggered flares.

LL-37

Treatment of chronic non-healing wounds including venous leg ulcers and diabetic ulcers

LL-37 is particularly well-suited for individuals focused on treatment of chronic non-healing wounds including venous leg ulcers and diabetic ulcers. Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.

Immune defense against antibiotic-resistant bacterial infections (MRSA, Pseudomonas)

LL-37 is particularly well-suited for individuals focused on immune defense against antibiotic-resistant bacterial infections (mrsa, pseudomonas). Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.

Anti-biofilm strategies for chronic wound infections and medical device-associated infections

LL-37 is particularly well-suited for individuals focused on anti-biofilm strategies for chronic wound infections and medical device-associated infections. Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.

Boosting innate immune defense in immunocompromised or aging individuals

LL-37 is particularly well-suited for individuals focused on boosting innate immune defense in immunocompromised or aging individuals. Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.

Safety Profile

Side
effects

Pidotimod

Common

  • Gastrointestinal discomfort
  • Skin rash
  • Headache
  • Nausea
  • Diarrhea
  • Transient fever

Uncommon

  • Allergic reaction

Serious

  • Severe hypersensitivity reaction

LL-37

Common

  • Local site irritation
  • Transient stinging or burning
  • Mild perilesional erythema
  • Increased wound exudate

Uncommon

  • Allergic contact reaction

Serious

  • Hemolytic activity at systemic concentrations

Research Status

Safety
& evidence

Pidotimod

Evidence Level

Moderate human trials (Phase 1-2)

FDA Status

Research compound

Safety Overview

Pidotimod (immuno-stimulating dipeptide analog) has 40+ years of safety data in European/Asian markets with favorable tolerability profile. Mild gastrointestinal effects occur in <5% of users; no serious adverse events in 25 years of clinical use across 50,000+ patient population. Oral bioavailability excellent with rapid intestinal absorption. No mutagenicity or carcinogenicity in preclinical testing; immunomodulatory mechanism carries theoretical risk in severely immunocompromised patients.

Contraindications

  • xKnown hypersensitivity to pidotimod or any excipients
  • xPregnancy and breastfeeding (insufficient safety data)
  • xChildren under 3 years of age
  • xSevere autoimmune disease in active flare

LL-37

Evidence Level

Moderate human trials (Phase 1-2)

FDA Status

Research compound

Safety Overview

LL-37 is an endogenous cathelicidin antimicrobial peptide naturally produced by immune cells and epithelial tissues, conferring inherent biocompatibility and low toxicity at physiological concentrations. Synthetic LL-37 shows excellent safety in in vitro immune assays and animal models with no hepatotoxicity, nephrotoxicity, or genotoxicity at relevant doses. At elevated concentrations, the cationic amphipathic structure can cause hemolysis and cell membrane damage, but therapeutic doses are far below these thresholds. Injection site reactions are minimal in research applications.

Contraindications

  • xKnown hypersensitivity to cathelicidin peptides or formulation components
  • xActive hemolytic conditions — LL-37 demonstrates concentration-dependent hemolytic activity
  • xPregnancy and breastfeeding — insufficient reproductive safety data from clinical trials
  • xSevere renal impairment — peptide clearance may be altered

Decision Guide

Which is
right for you?

Choose Pidotimod if...

  • Preventing recurrent respiratory tract infections
  • Supporting immune function in immunocompromised individuals
  • Reducing frequency of infections in children and elderly
  • Immune support during HIV management

Choose LL-37 if...

  • Treatment of chronic non-healing wounds including venous leg ulcers and diabetic ulcers
  • Immune defense against antibiotic-resistant bacterial infections (MRSA, Pseudomonas)
  • Anti-biofilm strategies for chronic wound infections and medical device-associated infections
  • Boosting innate immune defense in immunocompromised or aging individuals