Alzheimer's Disease
IND-enabling studies underway

The diagnostic and the treatment.
Together. For the first time.

Two companion biologics that visualize Alzheimer's with accuracy and treat it at the source — unified by AI. Our published preclinical animal-model data show reversal of cogntive deficits.

The approach

Diagnosis drives treatment

Alzheimer's has two devastating problems: we can't see it coming clearly enough, and we can't stop it once it starts. ExQor tackles both simultaneously with a unified system.

The MRI diagnostic biologic reveals exactly where damage is occurring. That scan then drives the treatment — telling us precisely where to target, how much to give, and whether it's working. No guesswork, no population-level dosing.

"Approved antibody therapies such as lecanemab and donanemab are designed to slow progression. ExQor is pursuing a different goal — repair at the source — and our published preclinical animal-model data show reversal of cognitive deficits . Clinical efficacy in humans will be established in our clinical trials."

Both biologics use a clathrin-mediated transport mechanism to cross the blood-brain barrier non-invasively — a platform discovery that underpins the entire system.

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Non-invasive delivery

Simplified administration. No surgery, no infusion center required — with home-based delivery potential.

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Real-time monitoring

MRI scans confirm treatment response over time. Objective evidence, not subjective reporting.

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AI-guided precision

The AI platform scores individual risk and tailors dosing strategy — clinician decision support, fully documented.

Development status

Regulatory pathway

ExQor is in IND-enabling studies targeting Phase 1 first-in-human trials. Our regulatory strategy leverages the diagnostic biologic as the entry point under FDA's companion diagnostic framework, with the treatment biologic following in sequence.

Current stage: IND-enabling studies
FDA IND preparation in progress. Phase 1 first-in-human trial targeting enrollment. Companion diagnostic framework: diagnostic biologic as regulatory entry point.

Market & patient impact

The scale of the opportunity

For the approximately 55 million people worldwide living with dementia — and the 131.5 million projected by 2050 — ExQor's unified approach aims to shift the treatment paradigm from disease management toward disease modification and repair. This is the program's objective; it has not yet been demonstrated in humans.

MRI diagnostic accessibility and home-based delivery potential could democratize access to advanced neurological care, reducing the global economic burden currently projected to reach $1.6 trillion by 2050. (Source: The Lancet)

55M
people living with dementia worldwide today
131M
projected patients by 2050
$1.6T
projected global economic burden by 2050

Get in touch

We welcome inquiries from partners interested in our CNS diagnostic and therapeutic programs.

Email: info@exqor.com
Tel: +1 (617) 742-4422