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NRI

Development stage
Preclinical
Lead developer
Chugai Pharmaceutical
Modality
Fc-Fusion Proteins → Carrier/Scaffold Proteins → Recombinant Proteins and Enzymes, Gene Therapies, Antibody Fragments → Engineered Antibody Formats → Antibody-Based Therapeutics
Administration
Intraperitoneal
01

Overview

NRI (New Receptor Inhibitor of IL-6) is an experimental recombinant biologic agent developed by researchers at Saga University in collaboration with Chugai Pharmaceutical. It is a humanized anti-interleukin-6 receptor (IL-6R) agent engineered from the monoclonal antibody tocilizumab. The structure of NRI consists of a single-chain variable fragment (scFv) derived from the VH and VL regions of tocilizumab, which is dimerized by fusion to the Fc portion of human immunoglobulin G1 (IgG1). This single-gene design was specifically optimized for delivery via gene therapy vectors, such as adenovirus (Ad/CMV/NRI). NRI functions as an IL-6R antagonist, blocking the binding of IL-6 and inhibiting downstream signaling pathways critical for the progression of inflammatory diseases and certain malignancies. Preclinical studies have demonstrated its efficacy in inhibiting the growth of IL-6-dependent cell lines, such as multiple myeloma and Lennert's lymphoma, and achieving sustained therapeutic serum levels in mouse models following intraperitoneal administration.

Other names
New Receptor Inhibitor of IL-6Ad/CMV/NRI
02

Targets

IL-6R (Interleukin-6 receptor subunit alpha)

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