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A Fibroblast-Targeting Advanced Lead Mitigating Inflammation and Fibrosis in IBD

Project description

Targeting fibroblasts as a treatment for inflammatory bowel disease

Inflammatory bowel disease (IBD) is characterised by chronic inflammation that can lead to fibrosis with excessive scarring of the intestine caused by overactive fibroblasts. This process not only worsens chronic inflammation but also increases the risk of complications such as colon cancer. Current therapies mainly suppress inflammation without tackling fibroblast-driven fibrosis. The ERC-funded FIBROLEAD project introduces a pioneering oral therapy with the compound VM-313, shown to reduce inflammation and fibrosis in preclinical models. Researchers will validate the clinical and commercial potential of VM-313 by testing its safety and efficacy in animal models of IBD. Ultimately, the vision is to transform IBD treatment and improve treatment results.

Objective

Inflammatory bowel disease (IBD), which comprises Crohn's disease (CD) and ulcerative colitis (UC), is a growing global health challenge affecting over 6.8 million people. Characterized by chronic inflammation leading to intestinal fibrosis, IBD significantly reduces quality of life and increases the risk of severe complications, including colon cancer. Current treatments primarily target inflammation, and fail to address the persistent activation of inflammatory fibroblast phenotypes and the resulting fibrosis, contributing to frequent relapses and a heightened risk of disease progression.
To address this gap, FIBROLEAD introduces a pioneering approach by targeting fibroblasts, key mediators of chronic inflammation and fibrosis in IBD. Our recent research identified VM-313 to effectively disrupt pathogenic fibroblast activation. We now have evidence that this compound has a strong potential in mitigating both inflammation and fibrosis in vitro, ex vivo and in a mouse model of lung fibrosis. Additionally, it exhibits a favourable safety/toxicity profile and drug-like properties that are equal or superior to currently available anti-fibrotic drugs. These findings position VM-313 as a promising candidate for expanding and improving therapeutic strategies for IBD and other fibrotic diseases.
This PoC project aims to develop VM-313 as an advanced lead and validate its clinical and commercial potential. Our approach includes assessing its in vivo safety and efficacy in animal models of IBD and determining its mode of action via target identification and validation studies. In parallel, we will develop a comprehensive business case, engage with key stakeholders, and conduct a commercial assessment to evaluate market entry potential. By leveraging our unique targeting strategy and the advantages of a non-invasive oral therapy, VM-313 has the potential to transform IBD treatment, delivering significant benefits to patients.

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HORIZON-ERC-POC - HORIZON ERC Proof of Concept Grants

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Call for proposal

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(opens in new window) ERC-2025-POC

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Host institution

INOLYSIS MONOPROSOPI IDIOTIKI KEFALAIOUCHIKI ETAIREIA
Net EU contribution

Net EU financial contribution. The sum of money that the participant receives, deducted by the EU contribution to its linked third party. It considers the distribution of the EU financial contribution between direct beneficiaries of the project and other types of participants, like third-party participants.

€ 150 000,00
Address
TRAPEZOUNTOS 17
151 27 MELISSIA ATHENS
Greece

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SME

The organization defined itself as SME (small and medium-sized enterprise) at the time the Grant Agreement was signed.

Yes
Region
Αττική Aττική Βόρειος Τομέας Αθηνών
Activity type
Private for-profit entities (excluding Higher or Secondary Education Establishments)
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Total cost

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No data

Beneficiaries (1)

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