Drug intelligence / Profile preview

IMB216P

Development stage
Preclinical
Lead developer
ImmunoBiochem
Modality
PROTACs (E3 ligase recruitment) → Targeted Protein Degraders (TPDs) → Small Molecules, Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Bivalent/Multivalent Binders → Multivalent & Scaffold-Based Small Molecules → Small Molecules
Administration
Subcutaneous
01

Overview

IMB216P is a first-in-class degrader-antibody conjugate (DAC) developed by ImmunoBiochem for the treatment of chronic autoimmune and inflammatory diseases. It consists of a monoclonal antibody targeting the interleukin-7 receptor alpha (IL7RA/CD127) conjugated to a proteolysis-targeting chimera (PROTAC) payload that induces the degradation of Janus kinase 1 (JAK1) and Tyrosine kinase 2 (TYK2). By targeting IL7RA, IMB216P selectively delivers the degrader to pathogenic T cells while sparing regulatory T cells (Tregs), which typically express low levels of CD127. This targeted approach aims to provide potent immunosuppression with improved safety compared to systemic JAK inhibitors. The drug is currently in IND-enabling studies for indications including inflammatory bowel disease (IBD), psoriasis, and systemic lupus erythematosus.

Other names
IMB216PIMB-216PIMB 216P
02

Targets

JAK1 (Janus kinase 1)TYK2 (Tyrosine kinase 2)IL7R (Interleukin-7 Receptor)

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