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FDA clears C2N Diagnostics' first blood test for early Alzheimer's

Published

11 September 2026

Topic

opportunities

Sectors

Digital Health

Geography

United States

Source

Read at longevity.technology

Verified

Fusion42 · 11 September 2026 · Fusion42 review

The FDA has cleared C2N Diagnostics' PrecivityAD2 blood test for early detection of Alzheimer’s in symptomatic adults aged 40 and older, enabling a less invasive and more accessible diagnostic alternative to PET scans and spinal taps.

This Wire brief sits within Fusion42's coverage of Digital Health.

◆ The Wire takeaway

You can now bring early Alzheimer’s testing to symptomatic younger adults with a simple blood draw, avoiding costly scans and painful spinal taps. This clears the way for quicker patient diagnosis and earlier treatment starts that are critical for effective therapy.

Coverage

1 source · 11 Sep 2026

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Digital Healthalzheimersdiagnosticsblood-testFDA-clearancedigital-healthlongevity