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NuVasc is building the first precision-medicine platform for neurovascular lesions including brain arteriovenous malformations (bAVM) and aneurysms. We use endovascular-enabled molecular genomics and targeted therapeutics to change how neurovascular lesions are diagnosed, risk-stratified, and treated.

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Brain AVMs are the leading cause of hemorrhagic stroke in children, & can lead to permanent neurologic disability or death
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Treatment options are limited to brain surgery (requiring long hospitalization, if ruptured) or radiation therapy
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Many of the underlying biological pathways that cause brain AVMs have been implicated in cancer
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Pharmacological treatment of brain AVMs is not in use because there is no standard for genomic diagnosis of AVMs
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Scope: 18 in 100,000 people have a brain AVM and 1 in 50 people have an intracranial aneurysm
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Treatments are currently limited to high-risk craniotomy or radiation therapy, and risk of non-treatment is death or permanent disability
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Mutations in cerebrovascular lesions overlap with well-characterized targets in oncology (KRAS, BRAF, MEK, PI3KCA, etc.)
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Precision therapies exist, but clinicians lack a safe, reliable way to determine which patients will benefit
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Millions of patients have neurovascular lesions eligible for targeted therapies, with 50,000+ AVMs and over 1 million aneurysms in the US

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