Drug intelligence / Profile preview

ITMN-520

Development stage
Discontinued
Lead developer
InterMune
Modality
Small Molecules
Administration
Oral
01

Overview

ITMN-520 is a small molecule pirfenidone analog that was developed by InterMune for the treatment of idiopathic pulmonary fibrosis (IPF) and other fibrotic conditions. As a next-generation compound in InterMune's pulmonology portfolio, it was designed to improve upon the efficacy or safety profile of pirfenidone (Esbriet). Like its parent compound, ITMN-520 is thought to possess anti-fibrotic and anti-inflammatory properties, potentially through the modulation of transforming growth factor-beta (TGF-beta) and tumor necrosis factor-alpha (TNF-alpha) pathways. Development of the compound appears to have been discontinued or deprioritized following the regulatory success of pirfenidone and the subsequent acquisition of InterMune by Roche in 2014.

02

Targets

TNFA (Tumor necrosis factor alpha (soluble))TGFB1 (Transforming growth factor Beta-1 proprotein)

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