Drug intelligence / Profile preview

LBP-KP01

Development stage
Preclinical
Lead developer
Locus Biosciences
Modality
Frozen FMT → Fecal Microbiota Transplantation (FMT) → Microbiome Therapeutics, Microbial Metabolites → Microbiome-Derived Products → Microbiome Therapeutics, Synthetic Biology Platforms → Engineered Microbial Therapeutics → Microbiome Therapeutics, Genetically Modified Bacteria → Engineered Microbial Therapeutics → Microbiome Therapeutics, Microbial Proteins → Microbiome-Derived Products → Microbiome Therapeutics, Gene Silencing → Gene Therapies, Fresh FMT → Fecal Microbiota Transplantation (FMT) → Microbiome Therapeutics, Bacterial Strains → Single Strain Products → Live Biotherapeutic Products → Microbiome Therapeutics, Complex Communities → Multi-strain Products → Live Biotherapeutic Products → Microbiome Therapeutics, Yeast Strains → Single Strain Products → Live Biotherapeutic Products → Microbiome Therapeutics, Gene Editing → Gene Therapies, Defined Consortia → Multi-strain Products → Live Biotherapeutic Products → Microbiome Therapeutics, Gene Addition/Replacement → Gene Therapies
Administration
Intravenous, Intravesical
01

Overview

LBP-KP01 is a precision-engineered bacteriophage cocktail developed to target and eliminate Klebsiella pneumoniae, a bacterial pathogen responsible for complicated and recurrent urinary tract infections (UTIs), including those caused by antibiotic-resistant strains. The product utilizes a dual mechanism of action combining the natural lytic activity of bacteriophages with the DNA-targeting function of an engineered CRISPR-Cas3 system. This approach enables highly specific destruction of K. pneumoniae cells while sparing beneficial bacteria, offering potential advantages over traditional broad-spectrum antibiotics. LBP-KP01 is being developed by Locus Biosciences in partnership with CARB-X and has received funding support for preclinical development and early clinical trials[1][2][5][6].

Other names
CRISPR/Cas3-engineered bacteriophage
02

Targets

Klebsiella pneumoniae cell surface structures

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