Donanemab (LY3002813) Trial in Chinese Participants With Cognitively Unimpaired (Preclinical) Alz… (NCT07571161) | Clinical Trial Compass
Not Yet RecruitingPhase 3
Donanemab (LY3002813) Trial in Chinese Participants With Cognitively Unimpaired (Preclinical) Alzheimer's Disease
China140 participantsStarted 2026-04
Plain-language summary
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.
Who can participate
Age range55 Years – 80 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* A Telephone Interview for Cognitive Status - Modified (TICS-M) score indicative of intact cognitive function (cut-off score of 35 or higher)
* Clinical Dementia Rating-Global Score (CDR-GS) of 0
* A plasma P-tau result consistent with amyloid pathology
* A reliable study partner who:
* Provides written informed consent to participate in the study in their role
* Has frequent contact with the participant and is familiar with their overall function and behavior, including daily activities and cognitive abilities
* Is of legal age (18 years of age or older) to consent
* Is available to conduct functional scales
* Have adequate literacy, vision, and hearing for neuropsychological testing
Exclusion Criteria:
* Have mild cognitive impairment (MCI), dementia, or other significant neurodegenerative diseases that could affect cognition
* Have a serious or unstable illness (including cardiovascular, hepatic, renal, gastrointestinal, respiratory, endocrinologic, neurologic, psychiatric, immunologic, or hematologic disease, or other condition) that, in the investigator's opinion, could interfere with study analyses or result in a life expectancy of 5 years or fewer
* Have received active or passive immunization against amyloid beta (Aβ) in any other study
* Have current or prior use of prescription medications for treatment of MCI or AD
* Have any contraindications for magnetic resonance imaging (MRI), including claustrophobia or the presence of contrain…
What they're measuring
1
Time to Clinical Progression as Measured by Clinical Dementia Rating-Global Score (CDR-GS)
Timeframe: Baseline Up to Week 156
Trial details
NCT IDNCT07571161
SponsorEli Lilly and Company
Sponsor typeINDUSTRY
Study typeINTERVENTIONAL
Primary completion2030-04
Contact for this trial
Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or