The first ADC for BPDCN

A first-of-its-kind
treatment

DECNUPAZ is an IgG1-based ADC designed to target CD123, a protein overexpressed on BPDCN cells.1-3

DECNUPAZ delivers a payload that is a member of the IGN* class of cytotoxic molecules.1

*IGN=indolinobenzodiazepine pseudodimer

DECNUPAZ mechanism
of action

1Target and Bind

The IgG1 antibody portion of DECNUPAZ targets and binds to CD123 with high affinity. While DECNUPAZ binds with high affinity to CD123, it may also affect healthy cells.1,4

2Internalize and Release

Once bound, DECNUPAZ is internalized. The peptide linker undergoes lysosomal degradation, releasing the IGN payload (FGN849).1,5

3Attach and Alkylate

The IGN payload then alkylates DNA, which leads to singlestrand breaks, making it first in class.1,6

4Disrupt and Drive Cell Death

These single-strand breaks may trigger cell cycle arrest and apoptosis, leading to cell death.1

Because of the way DECNUPAZ works, it has been shown to have adverse reactions. The most common Grade 3–4 laboratory abnormalities seen with DECNUPAZ (≥10%) were decreased neutrophils, platelets, lymphocyte count, white blood cells, hemoglobin, and increased glucose.1

The IGN* payload has shown potency against tumor cells and potentially less cytotoxicity to normal bone marrow progenitors in a descriptive pre‑clinical study.1,4

ADC=antibody-drug conjugate; BPDCN=blastic plasmacytoid dendritic cell neoplasm; DNA=deoxyribonucleic acid; IgG1=immunoglobulin G1