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The resulting outputs allow clear demonstration of NXP002's potential to regulate four specific pathways that drive fibrotic disease. This includes core pathways, such as the TGF- ß pathway, but also evidences regulation of the WNT/ß-catenin and NLRP3 pathways, which are emerging as key disease progression pathways requiring suppression. The outputs also illustrate consistent translation from cell-based studies to clinical studies across multiple fibrotic organs, including the lung, in the resolution of extra cellular matrix deposition.
The Company has summarised its findings in a new document 'NXP002 Pathway and Translation Update' which is available via the following link http://www.rns-pdf.londonstockexchange.com/rns/7219A_1-2025-9-24.pdf and will be published on the Company's website.
The Company continues to have ongoing discussions with potential development partners and will further showcase NXP002 at the
Dr
"We await news on our
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+44 (0) 20 3003 8632 |
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+44 (0) 20 3934 6630 |
About
About IPF
IPF is a chronic lung disease characterised by progressive tissue scarring that prevents proper lung function. It is a progressive, fatal, age-associated lung disease affecting approximately three out of every one hundred thousand people in
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