Drug intelligence / Profile preview

orziloben

Development stage
Unknown
Lead developer
NorthSea Therapeutics
Modality
Small Molecules
Administration
Oral
01

Overview

Orziloben (NST-6179) is a synthetic, structurally engineered fatty acid (SEFA) analogue developed by NorthSea Therapeutics for the treatment of intestinal failure-associated liver disease (IFALD). As a medium-chain fatty acid derivative, it is designed to target metabolic and inflammatory pathways in the liver that are disrupted during long-term parenteral nutrition. Orziloben acts primarily as an agonist of the peroxisome proliferator-activated receptor alpha (PPARα), promoting fatty acid oxidation and reducing hepatic steatosis and inflammation. It is currently being evaluated in Phase 2 clinical trials as an oral therapy for adult patients with IFALD, a condition characterized by liver injury resulting from the lack of enteral nutrition and the components of parenteral nutrition.

Other names
orziloben
02

Targets

PPARG (Peroxisome proliferator-activated receptor gamma)GPR84PPARA (Peroxisome proliferator-activated receptor alpha)

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