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HeartRestore

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Next-generation heart bypass grafts to naturally restore cardiovascular function...

Next-generation heart bypass grafts to naturally restore cardiovascular function. Coronary Artery Disease is caused by narrowing of heart arteries that supply blood, often due to atherosclerosis. Coronary artery bypass grafting (CABG) is the gold standard surgery to treat it, and it commonly involves harvesting... see more

30/11/2024

ASML NETHERLANDS B...

4M€

Project Budget: 4M€

Project leader

ASML NETHERLANDS B.V. No se ha especificado una descripción o un objeto social para esta compañía.

PARTICIPATION DEPralty Sin fecha límite de participación.

Financing granted El organismo HORIZON EUROPE notifico la concesión del proyecto The day 2024-11-30

HORIZON-EIC-2021-ACCELERATOROPEN-01: EIC Accelerator Open 2021 Scope:The EIC Accelerator supports companies (principally start-ups and SMEs) to scale up high impac...

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Este proyecto no cuenta con búsquedas de partenariado abiertas en este momento.

Private Information

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1 Participantes

ASML NETHERLANDS B.V.

2.48M€ | Leader

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Project duration: 24 months Date Start: 2022-11-22
End date: 2024-11-30

Project leader

ASML NETHERLANDS B.V. No se ha especificado una descripción o un objeto social para esta compañía.

Project Budget 4M€

participation deadline Sin fecha límite de participación.

Project description Coronary Artery Disease is caused by narrowing of heart arteries that supply blood, often due to atherosclerosis. Coronary artery bypass grafting (CABG) is the gold standard surgery to treat it, and it commonly involves harvesting patient’s veins from the legs as grafts. This collection affects patients causing chronic pain and costly complications. It also has a high failure rate with >20% implants occluded after 1 year. Xeltis has developed a unique restorative vascular graft (XABG) that eliminates the need for vein harvesting. The implant provides a homing structure for cells in which cardiac and vascular tissues can be naturally restored, with the related advantages and benefits for patients and the healthcare system. We have proven our technology in first niche applications, as well as completed pre-clinical studies successfully for XABG. Now, we plan to perform a full clinical validation to obtain a CE mark in Europe and start market deployment and commercial up-scaling.

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