Drug intelligence / Profile preview

IB-DMD

Development stage
Preclinical
Lead developer
Innobioscience
Modality
Small Molecules
Administration
Oral, Injectable
01

Overview

IB-DMD is a small molecule drug candidate being developed by Innobioscience for the treatment of Duchenne Muscular Dystrophy (DMD) and skeletal muscular fibrosis. The compound is designed to inhibit the NF-κB/IKKβ signaling pathway and modulate key fibrotic mediators, including Connective Tissue Growth Factor (CTGF), Transforming Growth Factor beta 1 (TGF-β1), and Plasminogen Activator Inhibitor-1 (PAI-1). By targeting these pathways, IB-DMD aims to reduce chronic inflammation and muscle fibrosis, which are central to the progressive muscle degeneration seen in DMD. Preclinical studies suggest that IB-DMD can improve muscular function and reduce muscle damage and tearing. It is being developed in both oral and injectable formulations.

02

Targets

CTGF (Connective tissue growth factor)NF-κBPAI-1 (Plasminogen activator inhibitor type 1)TGFB1 (Transforming growth factor Beta-1 proprotein)

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