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BHV-1320

Development stage
Preclinical
Lead developer
Biohaven
Modality
PROTACs (E3 ligase recruitment) → Targeted Protein Degraders (TPDs) → Small Molecules, Bivalent/Multivalent Binders → Multivalent & Scaffold-Based Small Molecules → Small Molecules
Administration
Subcutaneous
01

Overview

BHV-1320 is an investigational extracellular protein degrader developed by Biohaven using its proprietary Molecular Degrader of Extracellular proteins (MoDE) platform. The therapy is a bifunctional molecule designed to selectively bind to Immunoglobulin G (IgG) and the asialoglycoprotein receptor (ASGPR) on the surface of hepatocytes. This recruitment facilitates the internalization and subsequent lysosomal degradation of circulating IgG, thereby reducing the levels of pathogenic autoantibodies. BHV-1320 is specifically engineered for subcutaneous administration, distinguishing it from the lead intravenous candidate BHV-1300, and is intended to provide a more patient-friendly maintenance therapy for chronic autoantibody-mediated autoimmune diseases such as Myasthenia Gravis, Chronic Inflammatory Demyelinating Polyneuropathy (CIDP), and Graves' disease.

Other names
IgG MoDE (Subcutaneous)
02

Targets

ASGPR (Asialoglycoprotein Receptor 1)

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