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peginterferon alfa-2b + nucleoside analog + Bacteroides fragilis + branched-chain amino acids

Development stage
Preclinical
Lead developer
Merck
Modality
Small Molecules, Defined Consortia → Multi-strain Products → Live Biotherapeutic Products → Microbiome Therapeutics, Microbial Metabolites → Microbiome-Derived Products → Microbiome Therapeutics, 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, Bacterial Strains → Single Strain Products → Live Biotherapeutic Products → Microbiome Therapeutics, Frozen FMT → Fecal Microbiota Transplantation (FMT) → Microbiome Therapeutics, Microbial Proteins → Microbiome-Derived Products → Microbiome Therapeutics, Complex Communities → Multi-strain Products → Live Biotherapeutic Products → Microbiome Therapeutics, Cytokines & Interferons → Recombinant Proteins and Enzymes
Administration
Subcutaneous, Oral
01

Overview

This combination therapeutic regimen is being investigated for the treatment of chronic hepatitis B virus (HBV) infection. It consists of standard-of-care antiviral therapy—peginterferon alfa-2b (an immune modulator) and a nucleoside analog (a viral polymerase inhibitor)—supplemented with the probiotic *Bacteroides fragilis* and branched-chain amino acids (BCAA). The rationale behind this combination is to enhance HBsAg clearance by modulating the gut microbiota and providing nutritional support to improve the host's immune response against the virus. The study is being conducted by the First Affiliated Hospital of Fujian Medical University.

Other names
PegIFNα2b + nucleoside analog + Bacteroides fragilis + branched-chain amino acids
02

Targets

IFNAR2 (Interferon alpha/beta receptor subunit 2)IFNAR1 (Interferon alpha/beta receptor 1)

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