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Assessment of Safety, Tolerability, and Pharmacodynamic Effects of LY2886721 in Patients with Mild Cognitive Impairment Due to Alzheimer's Disease or Mild Alzheimer's Disease

Phase 1
Recruiting
Conditions
Mild Cognitive Impairment due to Alzheimer's Disease or mild Alzheimer Disease
Registration Number
JPRN-jRCT2080221890
Lead Sponsor
Eli Lilly Japan K.K.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
recruiting
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

1.Presents gradual and progressive change in memory function reported by participant or partner over more than 6 months
2.Meets criteria for MCI due to AD or Mild AD based on Free and Cued Selective Reminding score with Immediate Recall (FCSRT-IR) of greater than or equal to 16 for free recall or greater than or equal to 40 for total recall
3.Clinical Dementia Rating Scale (CDR) score of 0.5 or 1, memory box score of less than or equal to 0.5
4.Mini Mental State Examination (MMSE) score of 20-30
5.florbetapir F18 scan positive for the presence of amyloid beta
6.Women must be postmenopausal

Exclusion Criteria

Not provided

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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