Drug intelligence / Profile preview

Fp-EVs-msRNA4486

Development stage
Preclinical
Lead developer
Shanghai Children’s Hospital
Modality
Defined Consortia → Multi-strain Products → Live Biotherapeutic Products → Microbiome Therapeutics, Microbial Metabolites → Microbiome-Derived Products → Microbiome Therapeutics, Lipid-based Nanoparticles → Nanoparticles → Drug Delivery Systems, Synthetic Biology Platforms → Engineered Microbial Therapeutics → Microbiome Therapeutics, Fresh FMT → Fecal Microbiota Transplantation (FMT) → Microbiome Therapeutics, Genetically Modified Bacteria → Engineered Microbial Therapeutics → Microbiome Therapeutics, Yeast Strains → Single Strain Products → Live Biotherapeutic Products → Microbiome Therapeutics, Frozen FMT → Fecal Microbiota Transplantation (FMT) → Microbiome Therapeutics, Bacterial Strains → Single Strain Products → Live Biotherapeutic Products → Microbiome Therapeutics, Microbial Proteins → Microbiome-Derived Products → Microbiome Therapeutics, RNA Therapeutics → Nucleic Acid Therapeutics, Complex Communities → Multi-strain Products → Live Biotherapeutic Products → Microbiome Therapeutics
Administration
Oral
01

Overview

Fp-EVs-msRNA4486 is an experimental therapeutic agent consisting of extracellular vesicles (EVs) derived from the commensal gut bacterium *Faecalibacterium prausnitzii* (Fp) that carry a specific microbial small RNA, msRNA4486. Developed by researchers at Shanghai Children’s Hospital, this asset is being investigated for the treatment of inflammatory bowel disease (IBD), specifically colitis. The drug works by inhibiting the activation of the MAPKs/NF-κB and NLRP3 inflammatory signaling pathways in intestinal epithelial cells and suppressing the differentiation of pro-inflammatory Th17 cells. In preclinical studies using DSS and TNBS-induced colitis models, Fp-EVs-msRNA4486 demonstrated the ability to reduce weight loss, improve disease activity index scores, and ameliorate colonic epithelial injury and inflammatory cell infiltration.

Other names
Extracellular Vesicle-derived msRNA4486 from Faecalibacterium Prausnitzii
02

Targets

NF-κBNLRP3 (Nod-like receptor family pyrin domain-containing protein 3)MEK

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