A Study of Remternetug Versus Placebo in Early Alzheimer's Disease Participants at Risk for Cognitive and Functional Decline

What is this Study about?

The purpose of this study is to measure the difference in time to developing or worsening memory, thinking, or functional problems due to Alzheimer's disease occurring in participants receiving study drug compared to placebo.

Participation could last up to 255 weeks including screening, a double-blind treatment period, and a double-blind observation period. In addition, eligible participants who receive placebo during the double-blind treatment period may choose to extend their study participation to receive open-label remternetug in an extension period.

What Will Happen in This Study?

Participant will take the study drug by subcutaneous injection.  
Planned duration of treatment is 255 weeks.

Who is Eligible to Participate in this Study?

Male or female participants aged 65 to 80 years of age 
Minimal to no cognitive/functional impairment at Screening
Must have a study partner

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