A Phase 2 Study to Evaluate Efficacy and Safety of AL002 in Participants With Early Alzheimer's Disease (INVOKE-2)
What is this Study about?
This is a phase 2, Randomized, Double-blind, Placebo-controlled, Multicenter Study that will assess efficacy and safety of AL002 administered intravenously (IV) in participants with Early Alzheimer's Disease.
What Will Happen in This Study?
Participants will receive drug treatment via IV in clinic on Day 1 and once every 4 weeks thereafter. The total duration of study participation for each participant will be up to approximately 115 weeks, including treatment period of a minimum of 48 weeks, and a maximum of 96 weeks.
Who is Eligible to Participate in this Study?
You are eligible to participate in this study if you meet the following criteria:
- 50-85 years old
- Diagnosis of early Alzheimer's Disease
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