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Roche, Eli Lilly get FDA nod for new Alzheimer's blood test

Published

25 August 2026

Topic

opportunities

Sectors

Diagnostics

Geography

United States

Source

Read at medtechdive.com

Verified

Fusion42 · 25 August 2026 · Fusion42 review

Roche and Eli Lilly have received FDA approval for a new blood test for Alzheimer's disease, which will also be offered by Labcorp and Quest Diagnostics following earlier CE mark certification.

This Wire brief sits within Fusion42's coverage of Diagnostics, and 5 sources have reported it between 24 Aug 2026 and 25 Aug 2026.

◆ The Wire takeaway

You need to act now if you develop diagnostic tools for neurodegenerative diseases since FDA approval for these blood tests opens US clinical markets widely. Labs like Labcorp and Quest are early distributors — partner or compete with them fast.

Coverage

5 sources · first reported 24 Aug 2026 · latest 25 Aug 2026

Related on Wire

Topics

DiagnosticsalzheimersdiagnosticsFDA-approvalblood-testRocheEli-Lilly