Fibrozumab: A bispecific antibody for cancer and fibrosis

Targeting:

Drug-Resistant Cancer Cells

Activated Fibroblasts

Angiogenic Endothelial Cells



Same mechanism, additional therapeutic opportunities

ONCOLOGY

Pancreatic cancer stroma

Disassembles CAF-built fibrotic matrix in vitro and in vivo; reduces stromal stiffness and reverses fibrosis hallmarks.

Selective for disease matrix
LUNG FIBROSIS

Lung fibrosis

Blocks fibronectin and collagen assembly by fibroblasts from IPF patients while sparing physiological matrix in healthy fibroblasts.

Spares normal fibroblast matrix
LIVER FIBROSIS

Liver fibrosis

Reduces fibrotic gene expression in human liver spheroids stimulated with a fibrotic cocktail; consistent with hepatic stellate cell biology.

Validated in human liver model

How can Fibrozumab target cancer and fibrosis?

Blocking the same targets on multiple cell types involved in drug resistance, cancer progression, and fibrosis:

Targeting triple-positive cancer cells:

Adjuvant PDAC after curative-intent resection.

An essential combination partner for resistance-prone targeted therapy.

Targeting fibrotic cells:

To disrupt tumor fibrosis by targeting cancer-associated fibroblast production of fibronectin.

Targeting angiogenic endothelial cells:

To suppress tumor-associated angiogenesis.