This study is a pre-screening process used to assess participants' potential eligibility for Roche interventional Alzheimer's disease studies.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
SCREENING
Masking
NONE
Enrollment
80,000
Participants will have their blood drawn and cognitive score measured by the ISLT.
Concentration of pTau217 in Blood on Day1
Time frame: Day 1
Cognitive score in ISLT on Day 1
Time frame: Day 1
Reference Study ID Number: WP45722 https://forpatients.roche.com/ No attachments to email below.
CONTACT
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CONTACT
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