Lucent Diagnostics Announces Collaboration with Tempus to Integrate Blood-Based Alzheimer’s Biomarker Testing into Clinical Workflows
Agreement supports the identification of patients eligible for Alzheimer’s disease biomarker testing through Tempus Next and enables neurologists to order LucentAD® Complete on Tempus’ clinical ordering platform
More than 7 million Americans are living with Alzheimer’s disease today, yet only a small fraction are evaluated for eligibility for approved treatments. The collaboration aims to narrow that gap by embedding clinical guideline-directed identification and blood-based biomarker testing options directly into clinical decision-making workflows used by neurologists.
“This collaboration represents an important step toward ensuring blood-based Alzheimer’s biomarker testing becomes part of routine clinical practice – without placing additional burden on providers,” said
Tempus Next is an AI-enabled care pathway intelligence platform that identifies care gaps and equips providers with actionable insights consistent with clinical guidelines at the point of care. While the Tempus Next Care Gap Program helps identify patients who may benefit from biomarker testing based on established clinical guidelines, clinicians have the option to order LucentAD Complete through existing EHR integrations.
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