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Quest Diagnostics to Offer FDA-Cleared Roche pTau217 Blood Test to Assess Alzheimer's ...

Published

26 August 2026

Topic

opportunities

Sectors

Health

Geography

United States

Source

Read at biobuzz.io

Verified

Fusion42 · 26 August 2026 · Fusion42 review

Quest Diagnostics will offer Roche’s FDA-cleared Elecsys pTau217 blood test, the first single-biomarker test able to both confirm and rule out amyloid pathology for Alzheimer's disease, integrating it with its own multi-biomarker panel for broader diagnostic use starting late 2026. This blood-based testing offers a less invasive, more accessible and cost-effective alternative to traditional PET scans or spinal tap diagnostics.

This Wire brief sits within Fusion42's coverage of Health, and 6 sources have reported it between 24 Aug 2026 and 26 Aug 2026.

◆ The Wire takeaway

You must adapt your neurodegenerative disease diagnostics to include blood biomarker tests cleared by the FDA, as these replace invasive scans and taps with a simpler model accessible in routine labs.

Coverage

6 sources · first reported 24 Aug 2026 · latest 26 Aug 2026

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Topics

Healthalzheimersblood-testingFDA-clearancediagnosticsbiomarkers