Fujirebio’s Lumipulse G Wins FDA Clearance as First Blood Test for Diagnosis of Alzheimer’s Disease
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Via libera della Fda americana al primo test del sangue per la diagnosi di Alzheimer. L'esame, dell'azienda statunitense Fujirebio Diagnostics, si chiama 'Lumipulse' ed è indicato per individuare precocemente le placche amiloidi associate alla malattia neurodegenerativa in adulti over 55 che presentano segni e sintomi della patologia. Il nuovo test offre un'opzione diagnostica meno invasiva rispetto alle metodiche tradizionali, spiega la Food and Drug Administration. L'analisi ha ricevuto la des
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Fujirebio Submits FDA Regulatory Filing for Lumipulse® G pTau 217/β-Amyloid 1-42 Plasma Ratio In-Vitro Diagnostic Test as an Aid to Identify Patients With Amyloid Pathology Associated With Alzheimer's Disease
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