promise | BraiN20®: A paradigm shift in Acute Ischemic Stroke (AIS) patient management

Summary
Acute Ischemic Stroke (AIS) represents 85% of strokes and is the 2nd leading cause of death and the leading cause of disability worldwide. Today, AIS patient management lies on imaging tools (multimodal CT/MRI) and scores to select patients for Endovascular treatment (EVT) – the gold standard. Still, its efficacy is limited to 46% due to the lack of tools to guide decision-making. BraiN20® is a non-invasive medical device class IIb that provides real-time monitoring of AIS patients’ brain viability, thereby predicting who will benefit from EVT. Time is Brain has the exclusive right to the IPR of a neurophysiological biomarker: N20, a SEP and surrogate of cerebral blood flow. TiB aims to implement the clinical trials to validate BraiN20®, acquire CE-Mark and FDA clearance, and bring it to market. By providing real-time and continuous monitoring of brain viability, BraiN20® will accelerate stroke management and predict EVT outcome and offer tailored care for each patient.
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More information & hyperlinks
Web resources: https://cordis.europa.eu/project/id/190126352
Start date: 01-05-2023
End date: 30-04-2026
Total budget - Public funding: 5 150 878,25 Euro - 2 500 000,00 Euro
Cordis data

Original description

Acute Ischemic Stroke (AIS) represents 85% of strokes and is the 2nd leading cause of death and the leading cause of disability worldwide. Today, AIS patient management lies on imaging tools (multimodal CT/MRI) and scores to select patients for Endovascular treatment (EVT) – the gold standard. Still, its efficacy is limited to 46% due to the lack of tools to guide decision-making. BraiN20® is a non-invasive medical device class IIb that provides real-time monitoring of AIS patients’ brain viability, thereby predicting who will benefit from EVT. Time is Brain has the exclusive right to the IPR of a neurophysiological biomarker: N20, a SEP and surrogate of cerebral blood flow. TiB aims to implement the clinical trials to validate BraiN20®, acquire CE-Mark and FDA clearance, and bring it to market. By providing real-time and continuous monitoring of brain viability, BraiN20® will accelerate stroke management and predict EVT outcome and offer tailored care for each patient.

Status

SIGNED

Call topic

HORIZON-EIC-2022-ACCELERATOROPEN-01

Update Date

31-07-2023
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Horizon Europe
HORIZON.3 Innovative Europe
HORIZON.3.1 The European Innovation Council (EIC)
HORIZON.3.1.0 Cross-cutting call topics
HORIZON-EIC-2022-ACCELERATOR-01
HORIZON-EIC-2022-ACCELERATOROPEN-01 EIC Accelerator Open