Drug intelligence / Profile preview

BNZ-1

Development stage
Phase 2
Lead developer
Equillium
Modality
PEGylated Peptides → Modified Peptides → Peptides, Small Molecules
Administration
Intravenous, Subcutaneous
01

Overview

BNZ-1 is a first-in-class, pegylated 19-mer peptide that acts as a selective and simultaneous inhibitor of the cytokines interleukin-2 (IL-2), interleukin-9 (IL-9), and interleukin-15 (IL-15) by blocking their binding to the common gamma chain (\(\gamma_c\)) receptor subunit. This mechanism disrupts signaling pathways implicated in multiple T-cell malignancies and autoimmune diseases. BNZ-1 has demonstrated clinical proof-of-concept in cutaneous T-cell lymphoma (CTCL) with favorable safety, tolerability, and clinically meaningful improvements in disease scores. It is also being developed for alopecia areata. The drug was originally developed by Bioniz Therapeutics and later acquired by Equillium[1][2][3][4][5][7].

Brand names
EQ101EQ-101EQ 101
Other names
BNZ-1BNZ1BNZ 1BNZ132-1BNZ-132-1BNZ 132-1BNZ132-1-40BNZ-132-1-40BNZ 132-1-40EQ-101EQ101EQ 101
02

Targets

IL-15R (Interleukin 15 receptor alpha/interleukin 15 complex)IL-2R (Interleukin-2/interleukin-15 receptor complex)IL9R (Interleukin-9 receptor)

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