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Efficacy and Safety of LY451395 in Patients With Probable Alzheimer's Disease

Efficacy and Safety of LY451395 in Patients With Probable Alzheimer's Disease

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00051909
Enrollment
200
Registered
2003-01-20
Start date
2002-11-30
Completion date
2003-06-30
Last updated
2006-07-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alzheimer's Disease

Keywords

Alzheimer's Disease

Brief summary

Study of an investigational medication for the treatment of Alzheimer's Disease in patients who are not taking Aricept, Reminyl, Exelon.

Interventions

Sponsors

Eli Lilly and Company
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Must have a clinical diagnosis of Alzheimer's Disease * Must be at least 50 years of age * Must fluently read and speak English * Must have a reliable caregiver

Exclusion criteria

* Has serious health problems other than Alzheimer's Disease * Cannot swallow whole pills * Has had a menstrual period in the last two years * Takes insulin for diabetes * Has taken Aricept, Reminyl, or Exelon in the last 5 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026