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FDA clears blood test to aid evaluation for Alzheimer's disease
The U.S. Food and Drug Administration (FDA) has cleared an innovative blood test for marketing.
AI Summary
The U.S. Food and Drug Administration cleared a new blood test for marketing. The test, called PrecivityAD2, uses technology invented at Washington University School of Medicine in St. Louis to help diagnose Alzheimer’s disease early. C2N Diagnostics, a WashU‑based startup, developed and validated the test before FDA approval.
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