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Preclinical in vivo validation of a glioblastoma neuro snooper electrical device

Project description

Brain implant for post-tumour resection monitoring

Glioblastoma is an aggressive and fast-growing type of brain tumour that originates in the glial cells of the brain. It is highly resistant to standard treatments like surgery, radiation and chemotherapy, leading to poor prognosis and limited survival rates for patients. The ERC-funded GBM Neuro Snooper project aims to validate a proof-of-concept for a new medical device, the ‘GBM Neuro Snooper’. This device will profile in situ electrophysiology after tumour resection, offering new insights into brain tumour mechanisms and patient treatment strategies. Unlike existing devices, this miniaturised implant will be designed for moderate invasiveness. In the long term, this technology may also aid in advancing our understanding of conditions like epilepsy and Alzheimer’s disease.

Objective

Median survival for people that are diagnosed with glioblastoma (GBM) is only 15 months. Chemoradiotherapy and targeted therapies still fail to combat peritumoral relapse after tumour removal. Preventing peritumoral brain invasion is the main target to cure GBM. Our project aims to validate a proof-of concept for a new medical device (MD) GBM Neuro Snooper in GBM animal models, a required step before initiating a clinical trial (Technology Readiness Level from 2/3 to 4). This MD will allow to define an in-situ electrophysiology profile of patients with GBM, after the tumor resection, to access a new mechanistic understanding in the brain tumour field as well as, new strategies for patient stratification and treatment. Already existing MDs with electrode wires are either very stiff or with a millimetric dimension. The ERC work will lead to a first generic, miniaturised prototype implant with moderate invasiveness and which design was validated in connection with neurosurgeons for the GBM application, validation of its Freedom to Operate in the context of continuous IP landscaping and the creation of an exploitation plan. In a long-term perspective, it will help characterise hyperexcitability in brain diseases such as tumors, but also epilepsy or the Alzheimer Disease. We will also investigate the effect of stimulation of the peritumoral tissue and the correlation with the recorded signals as a new electro-theragnostic strategy. We will address the ethics and social dimension of using such a MD and our exploitation plan will include the protection of intellectual property, business strategy and the preparation of a clinical trial after project completion. The project will be performed by a dedicated team that includes significant expertise in technical development, preclinical validation of devices, surgery, and knowledge transfer.

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Programme(s)

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Topic(s)

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Funding Scheme

Funding scheme (or “Type of Action”) inside a programme with common features. It specifies: the scope of what is funded; the reimbursement rate; specific evaluation criteria to qualify for funding; and the use of simplified forms of costs like lump sums.

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

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Call for proposal

Procedure for inviting applicants to submit project proposals, with the aim of receiving EU funding.

(opens in new window) ERC-2023-POC

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Host institution

INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE
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
Total cost

The total costs incurred by this organisation to participate in the project, including direct and indirect costs. This amount is a subset of the overall project budget.

No data

Beneficiaries (1)

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