The main purpose of this study is to evaluate the effects of donanemab (LY3002813) versus placebo in Chinese participants who are at risk for decline of memory, language and physical ability to perform activities of daily living from Alzheimer's disease (AD). The study drug will be administered intravenously (IV) (into a vein in the arm). The study will last up to approximately 156 weeks, excluding screening.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
140
Time to Clinical Progression as Measured by Clinical Dementia Rating-Global Score (CDR-GS)
Time frame: Baseline Up to Week 156
Change From Baseline in Plasma Phosphorylated Tau at Threonine 217 (P-tau217)
Time frame: Baseline, Week 52
Change From Baseline as Measured by Clinical Dementia Rating-Sum of Boxes (CDR-SB)
Time frame: Baseline Up to Week 156
Pharmacokinetics (PK): Peak Concentrations of Serum Donanemab
Time frame: Baseline Up to Week 156
PK: Trough Concentrations of Serum Donanemab
Time frame: Baseline Up to Week 156
Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or
CONTACT
Physicians interested in becoming principal investigators please contact
CONTACT
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