C2N Diagnostics Receives $20M Program-Related Investment from GHR Foundation to Bring Alzheimer’s Blood Test to the Clinic
“A pressing need exists for affordable and accessible testing in dementia care,” stated
C2N expects to soon be able to provide practicing clinicians with a blood test that they can order for their patients who are showing early signs of memory loss. After a patient provides a sample of blood, the sample will be sent to C2N’s Clinical Laboratory Improvement Amendments (CLIA) certified lab facility for measurement. After analysis, C2N will report the results back to the patient’s doctor for sharing with the patient. The test will help doctors determine the likelihood that Alzheimer’s pathology is present. In addition to supporting C2N’s launch of the APTUS-Aβ™ test under CLIA, GHR’s funding will also fuel C2N’s global growth and pipeline of other neurologic diagnostic tests.
“C2N’s entrepreneurial mindset combined with their deep commitment to help patients are central to GHR’s goal of Alzheimer’s prevention,” stated
About APTUS™-Aβ
The APTUS™-Aβ blood test is an in vitro diagnostic under development for predicting brain amyloidosis as determined by PET scan results. It currently combines mass spectrometry-based quantification of plasma amyloid beta (Aβ) isoforms Aβ42 and Aβ40, ApoE status, and age to provide a probability score for the presence of amyloid pathology. C2N has shown that a lower plasma Aβ42/Aβ40 ratio correlates with brain amyloidosis determined by amyloid PET scans as well as other methods. Amyloid PET scans accurately detect amyloid plaques – one of the hallmarks of Alzheimer’s disease – and are used in the work up and management of people with cognitive impairment who are being evaluated for Alzheimer’s disease and other causes of cognitive decline. In early 2019, C2N was granted Breakthrough Device Designation for the APTUS™-Aβ test from the
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