Drug intelligence / Profile preview

LYS006

Development stage
Phase 2
Lead developer
Novartis
Modality
Small Molecules
Administration
Oral
01

Overview

LYS006 is a novel, highly potent and selective small molecule inhibitor of leukotriene A4 hydrolase (LTA4H), the final and rate-limiting enzyme in the biosynthesis of pro-inflammatory leukotriene B4 (LTB4). By inhibiting LTA4H, LYS006 suppresses the production of LTB4, a key mediator in neutrophil-driven inflammatory diseases. The drug has demonstrated strong pharmacodynamic effects with high selectivity and long-lasting inhibition of its target at low exposures. It is being developed for several neutrophil-driven inflammatory conditions including hidradenitis suppurativa, inflammatory acne, ulcerative colitis, and non-alcoholic steatohepatitis (NASH). Clinical studies have shown that it is well-tolerated with no dose-limiting toxicity up to the highest doses tested[1][2][3][4]. Developed by Novartis.

02

Targets

LTA4H (Leukotriene A4 hydrolase)

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