FDA greenlights first blood test to diagnose Alzheimer's disease

1 month ago 5
FDA headquarters in Washington DC.

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The Food and Drug Administration (FDA) has cleared Lumipulse G for U.S. commercialization as the first blood-based test that could help in the diagnosis of Alzheimer’s disease.

Developed by Pennsylvania-based Fujirebio Diagnostics, Lumipulse G received the FDA’s 510 ((k)) clearance on Friday

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