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Completed

Mild Alzheimer's, Mild Cognitive Impairment

A Study of LY3002813 in Participants With Memory Damage Due to Alzheimer's Disease (AD) or AD

AACD | {{ defaultRegistry.registryAnchorText }} NCT02624778 {{ currentLocaleObject.registryAnchorText }}

Study Purpose

The purpose of this study is to evaluate the effect of LY3002813 on brain scans, evaluate the safety of LY3002813 by looking at adverse events (side effects) and to look at the effect of LY3002813 on the body. The study is for research purposes only and is not intended to treat any medical condition.

Completed Study

The results of this study are not yet available.

Time Commitment

Your participation could last up to 84 weeks and include 27 visits to the study center.

Who Participated? Tool Tip Icon

Here you can find out a bit more about the requirements for volunteers who took part in this study

Gender

Male Female

Age

50+ years
  • Participant must present with mild cognitive impairment (for example, minor problems with mental abilities such as memory or thinking) due to Alzheimer's disease (AD) or mild-to-moderate Alzheimer's disease (AD)

  • Female participant must not be of childbearing potiential (for example, has had hysterectomy or without menstruation for at least 1 year)

  • Participant must have up to 2 reliable study partners who are in frequent contact with the participant, will accompany the participant to the office and/or be available by telephone at designated times, will monitor administration of prescribed medications and provide a separate written informed consent to participate

  • Participant must not have a history of bleeding inside the brain, carotid artery occlusion, stroke or epilepsy

  • Participant must not have gamma globulin therapy (IVIG) within the last year

  • Participant must be willing and able to undergo an MRI (magnetic resonance imaging)

Where This Study Took Place Tool Tip Icon

Where This Study Took Place Tool Tip Icon

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