If you are a device manufacturer dealing with the limitations of current post-MI interventions — this project developed a minimally invasive endocardial catheter that delivers a specialized hydrogel to prevent irreversible cardiac remodelling.
Bio-absorbable Heart Patch and Delivery System to Prevent Post-Heart Attack Scarring
Imagine a heart attack as a burn that leaves a permanent scar, making the heart stiff and weak. This technology acts like a smart, temporary scaffold that supports the heart wall and blocks scar tissue from forming. Once the heart heals, the material simply dissolves safely into the body.
What needed solving
Current treatments for heart attacks fail to prevent scar tissue and cardiac remodelling, leaving millions of patients at risk of heart failure.
What was built
A recombinant elastin-like hydrogel and a matching minimally invasive endocardial catheter, supported by GMP manufacturing protocols.
Who needs this
Who can put this to work
If you are a biotech firm dealing with the difficulty of scaling lab-grade hydrogels — this project developed GMP manufacturing SOPs and a fed-batch synthesis method for elastin-like recombinant hydrogels.
If you are a healthcare provider dealing with the high cost of treating 26.5 million IHD patients in Europe — this project developed a therapeutic intervention to reduce heart failure risk and long-term patient burden.
Quick answers
What is the cost or pricing model for this treatment?
Based on available project data, specific pricing is not provided, but the project is developing a health economic evaluation to assess potential savings and patient benefits.
Can this be produced at an industrial scale?
Yes, the project is currently refining production using a fed-batch hydrogel synthesis method and has documented Standard Operating Procedures (SOPs) for GMP manufacturing.
What is the status of the IP and licensing?
The project is actively developing intellectual property rights (IPR) strategies in preparation for first-in-human validation studies.
What regulatory hurdles are being addressed?
The consortium is developing regulatory strategies to move the hydrogel and catheter toward a first-in-human (FIH) validation study.
What is the timeline for clinical use?
The project runs until 2026-11-30, aiming to reach the preparedness level for a first-in-human study by the end of the period.
Who built it
The consortium is highly commercially oriented, with a 50% industry ratio consisting of 4 industrial partners, including 3 SMEs. This balance between 3 universities and 1 research institute suggests a strong push toward translation, specifically focusing on GMP manufacturing and catheter delivery systems.
Contact the University of Galway for details on the ELR-SCAR preclinical validation results.
Talk to the team behind this work.
Contact us to explore licensing opportunities for the ELR-hydrogel GMP processes.