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Alzheimer's blood test developed by Roche, Lilly gets FDA clearance
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Fusion42 · 25 August 2026 · Fusion42 review
The FDA has granted clearance to a new blood test for Alzheimer's disease developed by Roche and Lilly, representing a significant advancement in early and non-invasive diagnosis.
This Wire brief sits within Fusion42's coverage of Biotech, and 3 sources have reported it between 24 Aug 2026 and 25 Aug 2026.
◆ ◆ The Wire takeaway
Your Alzheimer's diagnostic startup now faces competition from a clinically authorised blood test; accelerating non-invasive diagnostic offerings can secure your position before market expectations shift.
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3 sources · first reported 24 Aug 2026 · latest 25 Aug 2026
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