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Novel MetaP2 Inhibitors for Treatment of Age-Related Macular Degeneration

Benny Ofra , HUJI, School of Medicine - IMRIC, School of Pharmacy- Institute for Drug Research

Category

Life Sciences and Biotechnology   

Keywords

AMD, Angiogenic, VEGF, METAP2

Current development stage

TRL3 Experimental proof of concept      

 

Application

Age Related Macular Degeneration (AMD) is the leading cause of blindness in elderlies in the western world and an increasingly growing problem. The global AMD and diabetic retinopathy treatment market is overwhelmingly dominated by the high-cost injectable anti-vascular endothelial growth factor (anti-VEGF) drugs, including Lucentis, Avastin, and Eylea. However, these treatments are restricted to a single growth factor and mainly affecting edema rather regressing blood vessels.  As a result, the treatments become less effective over time due to compensating mechanisms.

It is considered that a broad spectrum inhibitors of angiogenesis based on Methionine Aminopeptidase 2 (MetAp2) inhibition may affect downstream signals to VEGF and thus lead to higher potency of the treatments.

Our Innovation

Using synthetic chemistry, novel compounds with high ability to block MetAp2 activity were synthesized. These compounds have a potential for use as anti-angiogenic drugs in different vascular pathologies, and specifically in AMD.

Advantages

  • Broad spectrum application
  • Lower potency of treatments
  • Small molecule drug
  • No need for repeated injections

Clinical Results

In-vitro: Molecules have been synthesized and tested in MetAp2 inhibition and in cell assays (inhibited proliferation of endothelial cells).

Opportunity

The synthetic compounds have a potential for use as anti-angiogenic drugs in vascular pathologies, including cancer, inflammatory diseases, obesity, dermal diseases, ocular diseases, arthritis etc. Potentially also relevant to autoimmune diseases and obesity.

 

Contact for more information:

Ariela Markel
VP, Business Development, Healthcare
+972-2-6586608
Contact ME:
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