Therapeutics
Anti-LOX for the Treatment of Duchenne, Fibrosis and Cancer (No. T4-1913)

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Overview

LOX is a key driver of fibrosis and tumor progression through its role in extracellular matrix remodeling. We developed a set of LOX inhibitors based on LOX’s natural prodomain (LPD) to treat fibrosis, Duchenne Muscular Dystrophy (DMD), and cancer.

Applications
  • Treatment of fibrotic diseases and metastatic cancer
  • Mutation-independent treatment of DMD
Differentiation
  • Selective: targets only extracellular LOX
  • Broad: applicable across a range of fibrotic diseases and cancer
  • Validated: in vivo efficacy in fibrosis and cancer mouse models
  • Stable: high-affinity Fc-fusion inhibitor
  • Antibody-like: durable and selective design
Development Stage
  • Fc- protein inhibitor purified, characterized for stability and high-affinity binding
  • Showed significant reduction in fibrosis and improved muscle function in DMD mice
  • Reduced lung metastases in a melanoma mouse model

LOX inhibitor

 

LOX inhibitors (LPD) reduced collagen deposits in the MDX Duchenne mouse model

Patent Status: 
USA Published: Publication Number: 20240398906 USA Published: Publication Number: 2022-0049236-A1
Full Professor Irit Sagi

Irit Sagi

Faculty of Biology
Immunology and Regenerative Biology
All projects (3)
Contact for more information

Dr. Tamar Farfel-Becker

Director of Business Development, Life Sciences

+972-8-9344546 Linkedin