
Improve Alzheimer’s disease detection with innovative, FDA-cleared PrecivityAD2 blood biomarker testing
Join Mayo Clinic Laboratories and C2N Diagnostics for our webinar exploring how the evolution of blood biomarker testing for Alzheimer's disease has expanded access to earlier, less-invasive diagnosis. Focusing on the newly FDA-cleared PrecivityAD2 blood test, which is offered by Mayo Clinic Laboratories in collaboration with C2N Diagnostics, the discussion will highlight how results from blood biomarker testing can support timely diagnosis, informed clinical decision-making, and improved patient care.
On Thursday, Oct. 29, from 11 a.m. to noon CT, learn more about the evolving diagnostic landscape of Alzheimer’s disease and why PrecivityAD2 testing is at the leading edge of early detection of amyloid pathology and Alzheimer’s disease diagnosis. This webinar is presented by Matthew Binnicker, Ph.D., chief scientific officer for Mayo Clinic Laboratories; Ronald Petersen, M.D., Ph.D., professor of neurology at Mayo Clinic; and Joel Braunstein, M.D., MBA, co-founder and CEO of C2N Diagnostics.
Don't miss this opportunity to learn how the latest clinical insights on Alzheimer’s disease diagnosis along with the noninvasive, PrecivityAD2 blood test can improve early detection for Alzheimer’s disease.
For questions, contact us at mcleducation@mayo.edu.