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Effects of LY450139, on the Progression of Alzheimer's Disease as Compared With Placebo (IDENTITY-2)

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Eli Lilly and Company
ClinicalTrials.gov Identifier:
NCT00762411
First received: September 26, 2008
Last updated: September 22, 2014
Last verified: September 2014
  Purpose

Alzheimer's disease (AD) is a fatal degenerative disease of the brain for which there is no cure. AD causes brain cells to die. AD is thought to be caused by an excess of beta amyloid (β-amyloid), a sticky protein in the brain that forms amyloid plaques. At autopsy, AD patients are required to have these amyloid plaques in the brain in order to have a definitive diagnosis of AD. Inhibiting the enzyme gamma-secretase (γ-secretase) lowers the production of β-amyloid. Semagacestat (LY450139) is a functional γ-secretase inhibitor and was shown to lower β-amyloid in blood and spinal fluid in humans tested thus far and in blood, spinal fluid and brain in animals tested thus far. This study used several different tests to measure the effect of semagacestat on both β-amyloid and amyloid plaques for some patients. The buildup of amyloid plaques was measured by a brain scan that takes a picture of amyloid plaques in the brain. Other tests measured the overall function of the brain and brain size in some patients. In this trial, patients who initially received placebo (inactive sugar pill) were, at a certain point in the study, switched over to active drug, semagacestat. In other words, all patients could eventually receive active drug. Each patient's participation could last approximately 2 years. Patients taking approved AD medications were permitted to participate in this study and continue taking these medications during the study. All patients who completed this study had the option to continue receiving semagacestat by participating in an open label study.

Preliminary results from this study (LFBC) (and another similar study LFAN [NCT00594568]) showed semagacestat did not slow disease progression and was associated with worsening of clinical measures of cognition and the ability to perform activities of daily living. Study drug was stopped in all studies. LFBC, LFAN and open label LFBF (NCT01035138) have been amended to continue collecting safety data, including cognitive scores, for at least seven months. The CT-Registry will reflect results of analyses from the original protocol in addition to those from the amended protocol.


Condition Intervention Phase
Alzheimer's Disease
Drug: LY450139
Drug: Placebo
Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Effect of LY450139 a y-Secretase Inhibitor, on the Progression of Alzheimer's Disease as Compared With Placebo

Resource links provided by NLM:


Further study details as provided by Eli Lilly and Company:

Primary Outcome Measures:
  • Change From Baseline in Alzheimer's Disease Assessment Scale- Cognitive Subscale (ADAS-Cog11) at 76 Weeks [ Time Frame: Baseline (randomization), 76 weeks ] [ Designated as safety issue: No ]
    The cognitive subscale of the ADAS (ADAS Cog11) was used as a primary efficacy measure and consists of 11 items assessing areas of function most typically impaired in Alzheimer's disease (AD): orientation, verbal memory, language, and praxis. The scale ranges from 0 to 70, with higher scores indicating greater disease severity. Least Squares (LS) Mean value was controlled for baseline value, age, investigator, visit, and concomitant standard of care (SOC) medication.

  • Change From Baseline in Alzheimer's Disease Assessment Scale- Cognitive Subscale (ADAS-Cog11) at 16 Weeks After Cessation of Study Drug [ Time Frame: Baseline (randomization), 16 weeks following treatment cessation ] [ Designated as safety issue: Yes ]
    The cognitive subscale of ADAS (ADAS Cog11) consists of 11 items assessing areas of function most typically impaired in Alzheimer's disease (AD): orientation, verbal memory, language, and praxis. The scale ranges from 0 to 70, with higher scores indicating greater disease severity. Least Squares (LS) Mean value was controlled for baseline value, age, investigator, visit, and concomitant standard of care (SOC) medication.

  • Change From Baseline in Alzheimer's Disease Cooperative Study Activities of Daily Living Inventory (ADCS-ADL) at 76 Weeks [ Time Frame: Baseline (randomization), 76 weeks ] [ Designated as safety issue: No ]
    The ADCS-ADL is a 23-item inventory developed as a rater-administered questionnaire answered by the participant's caregiver. The ADCS-ADL measures both basic and instrumental activities of daily living by participants. The total score ranges from 0 to 78, with lower scores indicating greater disease severity. Least Squares (LS) Mean value was controlled for baseline value, age, investigator, visit, and concomitant standard of care (SOC) medication.

  • Change From Baseline in Alzheimer's Disease Cooperative Study Activities of Daily Living Inventory (ADCS-ADL) at 16 Weeks After Cessation of Study Drug [ Time Frame: Baseline (randomization), 16 weeks following treatment cessation ] [ Designated as safety issue: Yes ]
    The ADCS-ADL is a 23-item inventory developed as a rater-administered questionnaire answered by the participant's caregiver. The ADCS-ADL measures both basic and instrumental activities of daily living by participants. The total score ranges from 0 to 78, with lower scores indicating greater disease severity. Least Squares (LS) Mean value was controlled for baseline value, age, investigator, visit, and concomitant standard of care (SOC) medication.


Secondary Outcome Measures:
  • Change From Baseline in Clinical Dementia Rating (Sum of Boxes; CDR-SB) at 76 Weeks [ Time Frame: Baseline (randomization), 76 weeks ] [ Designated as safety issue: No ]
    CDR-SB is a semi-structured interview of participants and their caregivers. Participant's cognitive status is rated across 6 domains of functioning, including memory, orientation, judgment/problem solving, community affairs, home/hobbies, and personal care. Severity score assigned for each of 6 domains; total score (SB) ranges from 0 to 18. Higher scores indicate greater disease severity. Least Squares (LS) Mean value was controlled for baseline value, age, investigator, visit, and concomitant standard of care (SOC) medication.

  • Change From Baseline in Neuropsychiatric Inventory (NPI) at 76 Weeks [ Time Frame: Baseline (randomization), 76 weeks ] [ Designated as safety issue: No ]
    NPI assesses psychopathology in participants with dementia and other neurologic disorders. Information is obtained from a caregiver familiar with the participant's behavior. Total score ranges from 12 to 144; higher scores indicate greater disease severity. Least Squares (LS) Mean value was controlled for baseline value, age, investigator, visit, and concomitant standard of care (SOC) medication.

  • Change From Baseline in the Resource Utilization in Dementia-Lite (RUD-Lite) up to 76 Weeks [ Time Frame: Baseline (randomization), up to 76 weeks ] [ Designated as safety issue: No ]
    Assesses healthcare resource utilization (formal and informal care). Information gathered on both caregivers (care-giving time, work status) and participants (accommodation and healthcare resource utilization) was gathered from baseline and follow-up interviews. Reported number of hospitalizations per participant up to 76 weeks. Least Squares (LS) Mean value was controlled for age and investigator.

  • Change From Baseline in the EuroQol 5-Dimensional Health-Related Quality of Life Scale Proxy Version (EQ-5D Proxy) Visual Analog Scale (VAS) at 76 Weeks [ Time Frame: Baseline (randomization), 76 weeks ] [ Designated as safety issue: No ]
    EQ-5D (proxy version) measures mobility, self-care, usual activities, pain/discomfort, anxiety/depression; each has 3 severity levels (no, some, severe problems) coded to a 1-digit number (1-3). Digits are combined into 5-digit number describing health state. Numerals 1-3 are not added for total score. VAS assesses caregiver's impression of participant's overall health state; scores range: 0 to 100. Lower scores indicate greater disease severity. Least Squares (LS) Mean value controlled for baseline value, age, investigator, visit, and concomitant standard of care (SOC) medication.

  • Change From Baseline in Quality of Life in Alzheimer's Disease (QoL-AD) at 76 Weeks [ Time Frame: Baseline (randomization), 76 weeks ] [ Designated as safety issue: No ]
    Assess QoL for AD: participant rates mood, relationships, memory, finances, physical condition, and overall QoL assessment. Each of 13 items, rated on a 4-point scale. Sum of items=total score (range: 13 to 52). Higher scores indicate greater QoL. Participant's primary caregiver asked to complete same measure. Least Squares (LS) Mean value controlled for baseline value, age, investigator, visit, and concomitant standard of care (SOC) medication.

  • Change From Baseline in Mini Mental State Examination (MMSE) at 76 Weeks [ Time Frame: Baseline (randomization), 76 weeks ] [ Designated as safety issue: No ]
    MMSE is a brief screening instrument used to assess cognitive function (orientation, memory, attention, ability to name objects, follow verbal/written commands, write a sentence, and copy figures) in elderly participants. Total score ranges from 0 to 30; lower score indicates greater disease severity. Least Squares (LS) Mean value was controlled for baseline value, age, investigator, visit, and concomitant standard of care (SOC) medication

  • Percent Change From Baseline in Amyloid Beta (Aβ) 1-42 Plasma Concentration at 52 Weeks [ Time Frame: Baseline (randomization), 52 weeks ] [ Designated as safety issue: No ]
    Concentration of amino acid peptide known as Aβ 1-42 in plasma. Least Squares (LS) Mean value was controlled for baseline value, age, and investigator.

  • Change From Baseline in Positron Emission Tomography (PET) Using Fluorine-18 Fluorodeoxyglucose (18F-FDG) at 76 Weeks [ Time Frame: Baseline (randomization), 76 weeks ] [ Designated as safety issue: No ]
    Measurement of local cerebral glucose metabolism by PET using the radioactive tracer 18F-FDG. The outcome reported is the composite summary of the standard uptake value ratio (SUVR) normalized to the Pons. Least Squares (LS) Mean value was controlled for baseline value, age, and investigator.

  • Change From Baseline in Hippocampal Volume Using Volumetric Magnetic Resonance Imaging (vMRI) up to 76 Weeks [ Time Frame: Baseline (randomization), up to 76 weeks ] [ Designated as safety issue: No ]
    The vMRI assessment of right and left hippocampal volume is reported. Least Squares (LS) Mean value was controlled for baseline value, age, and investigator.

  • Change From Baseline in Amyloid Imaging Positron Emission Tomography (AV-45 PET) up to 76 Weeks [ Time Frame: Baseline (randomization), up to 76 weeks ] [ Designated as safety issue: No ]
    A radioactive tracer for PET that is a ligand for amyloid called [18F]-AV-45. This permits the visualization of amyloid in the brains of Alzheimer's participants. The outcome reported is the composite summary of the standard uptake value ratio (SUVR) normalized to the cerebellar gray matter. Least Squares (LS) Mean value was controlled for baseline value, age, and investigator.

  • Change From Baseline in Tau Concentration in Spinal Fluid up to 76 Weeks [ Time Frame: Baseline (randomization), up to 76 weeks ] [ Designated as safety issue: No ]
    Concentration of total tau in spinal fluid. Least Squares (LS) Mean value was controlled for baseline value, age, and investigator.

  • LY450139 Population Pharmacokinetics: Clearance of LY450139 [ Time Frame: 6 weeks, 12 weeks, and 52 weeks ] [ Designated as safety issue: No ]
    Model estimated apparent oral clearance. Clearance is defined as the volume of plasma which is completely cleared of drug (LY450139) per unit time.

  • LY450139 Population Pharmacokinetics: Volume of Distribution of LY450139 [ Time Frame: 6 weeks, 12 weeks, and 52 weeks ] [ Designated as safety issue: No ]
    Model-estimated apparent volume of distribution. Volume of distribution is a measure of the extent to which drug distributes in the body.

  • Change From Baseline in Clinical Dementia Rating (Sum of Boxes; CDR-SB) at 4 Weeks After Cessation of Study Drug [ Time Frame: Baseline (randomization), 4 weeks following treatment cessation ] [ Designated as safety issue: Yes ]
    Semi-structured interview. Participant's cognitive status rated across 6 domains of functioning: memory, orientation, judgment/problem solving, community affairs, home/hobbies, personal care. Severity score assigned for each of 6 domains; total score (SB) ranges: 0 to 18. Higher scores=greater disease severity. Least Squares Mean value controlled for baseline value, age, investigator, visit, and concomitant standard of care medication. LY450139 dosing stopped due to evidence of dose-dependent cognitive/functional worsening. Participants followed off-dose for 32 weeks, but CDR-SB not assessed.

  • Change From Baseline in Neuropsychiatric Inventory (NPI) at 4 Weeks After Cessation of Study Drug [ Time Frame: Baseline (randomization), 4 weeks following treatment cessation ] [ Designated as safety issue: Yes ]
    NPI assesses psychopathology in participants with dementia and other neurologic disorders. Information is obtained from a caregiver familiar with participant's behavior. Total score ranges from 12 to 144; higher scores indicate greater disease severity. The Least Squares (LS) Mean value was controlled for baseline value, age, investigator, visit, and concomitant standard of care (SOC) medication. All LY450139 dosing stopped due to evidence of dose-dependent cognitive/functional worsening. Participants were followed off-dose for 32 weeks, but NPI was not assessed.

  • Change From Baseline in Resource Utilization in Dementia-Lite (RUD-Lite) at 4 Weeks After Cessation of Study Drug [ Time Frame: Baseline (randomization), 4 weeks following treatment cessation ] [ Designated as safety issue: Yes ]
    Assesses healthcare resource utilization (formal and informal care). Information gathered on both care-giving time, work status) and participants (accommodation, healthcare resource utilization) is collected. Reported number of participant hospitalizations. Least Squares (LS) Mean value controlled for age and investigator. All LY450139 dosing was stopped due to evidence of dose-dependent cognitive/functional worsening. Participants were followed off-dose for 32 weeks, but RUD-Lite was not assessed.

  • Change From Baseline in EuroQol 5-Dimensional Health-Related Quality of Life Scale Proxy Version (EQ-5D Proxy) Visual Analog Scale (VAS) at 4 Weeks After Cessation of Study Drug [ Time Frame: Baseline (randomization), 4 weeks following treatment cessation ] [ Designated as safety issue: Yes ]
    EQ-5D (proxy version) measures mobility, self-care, usual activities, pain/discomfort, anxiety/depression. 3 severity levels: no, some, severe problems. VAS assesses caregiver's impression of participant's health state; score ranges: 0 to 100. Lower scores=greater disease severity. Least Squares (LS) Mean value controlled for baseline value, age, investigator, visit, and concomitant standard of care (SOC) medication. All LY450139 dosing was stopped due to evidence of dose-dependent cognitive/functional worsening. Participants were followed off-dose for 32 weeks, but EQ-5D VAS was not assessed.

  • Change From Baseline in Quality of Life in Alzheimer's Disease (QoL-AD) at 4 Weeks After Cessation of Study Drug [ Time Frame: Baseline (randomization), 4 weeks following treatment cessation ] [ Designated as safety issue: Yes ]
    Assess QoL for AD; participant rates mood, relationships, memory, finances, physical condition, and overall QoL assessment. Each of 13 items rated on a 4-point scale. Sum of items=total score (range: 13-52). Higher scores=greater QoL. Participant's primary caregiver asked to complete same measure. Least Squares Mean value controlled for baseline, age, investigator, visit, and concomitant standard of care (SOC) medication. All LY450139 dosing was stopped due to evidence of dose-dependent cognitive/functional worsening. Participants were followed off-dose for 32 weeks, but QoL-AD not assessed.

  • Change From Baseline in Mini Mental State Examination (MMSE) 4 Weeks After Cessation of Study Drug [ Time Frame: Baseline (randomization), 4 weeks following treatment cessation ] [ Designated as safety issue: Yes ]
    Used to assess cognitive function (orientation, memory, attention, ability to name objects, follow verbal/written commands, write a sentence, and copy figures) in elderly participants. Total score ranges: 0 to 30. Lower score indicates greater disease severity. Least Squares (LS) Mean value was controlled for baseline value, age, investigator, visit, and concomitant standard of care (SOC) medication. All LY450139 dosing was stopped due to evidence of dose-dependent cognitive/functional worsening. Participants were followed off-dose for 32 weeks, but MMSE was not assessed.

  • Change From Baseline in Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS-Cog12) at 76 Weeks [ Time Frame: Baseline (randomization), 76 weeks ] [ Designated as safety issue: No ]
    ADAS-Cog12 is ADAS‑Cog11 augmented with delayed free recall measure, resulting in a total score ranging from 0 to 80. Higher scores indicate greater disease severity. Least Squares (LS) Mean value was controlled for baseline value, age, investigator, visit, and concomitant standard of care (SOC) medication.

  • Change From Baseline in Alzheimer's Disease Assessment Scale (ADAS-Cog14) at 76 Weeks [ Time Frame: Baseline (randomization), 76 weeks ] [ Designated as safety issue: No ]
    ADAS-Cog14 is ADAS-Cog11 augmented with delayed free recall, digit cancellation, and maze completion measures. A score of 0 to 10 for delayed free recall and a conversion code of 0 to 5 for digit cancellation and maze completion provide total score ranges for this extended ADAS-Cog14 of 0 to 90. Higher scores indicate greater disease severity. Least Squares (LS) Mean value was controlled for baseline value, age, investigator, visit, and concomitant standard of care (SOC) medication.

  • Change From Baseline in Phosphorylated-Tau (P-tau) Concentration in Spinal Fluid up to 76 Weeks [ Time Frame: Baseline (randomization), up to 76 weeks ] [ Designated as safety issue: No ]
    Concentration of p-tau in spinal fluid. Least Squares (LS) Mean value was controlled for baseline value, age, and investigator.

  • Change From Baseline in Amyloid Beta (Aβ) 1-42 Concentration in Spinal Fluid up to 76 Weeks [ Time Frame: Baseline (randomization), up to 76 weeks ] [ Designated as safety issue: No ]
    Concentration of an amino acid peptide known as Aβ 1-42 in spinal fluid. Least Squares (LS) Mean value was controlled for baseline value, age, and investigator.

  • Change From Baseline in Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS-Cog12) at 16 Weeks After Cessation of Study Drug [ Time Frame: Baseline (randomization), 16 weeks following treatment cessation ] [ Designated as safety issue: Yes ]
    ADAS-Cog12 is ADAS‑Cog11 augmented with delayed free recall measure, resulting in a total score ranging from 0 to 80. Higher scores indicate greater disease severity. Least Squares (LS) Mean value was controlled for baseline value, age, investigator, visit, and concomitant standard of care (SOC) medication.

  • Change From Baseline in Alzheimer's Disease Assessment Scale (ADAS-Cog14) at 16 Weeks After Cessation of Study Drug [ Time Frame: Baseline (randomization), 16 weeks following treatment cessation ] [ Designated as safety issue: Yes ]
    ADAS-Cog14 is ADAS-Cog11 augmented with delayed free recall, digit cancellation, and maze completion measures. A score of 0 to 10 for delayed free recall and a conversion code of 0 to 5 for digit cancellation and maze completion provide total score ranges for this extended ADAS-Cog14 of 0 to 90. Higher scores indicate greater disease severity. Least Squares (LS) Mean value was controlled for baseline value, age, investigator, visit, concomitant standard of care (SOC) medication.


Enrollment: 1111
Study Start Date: September 2008
Study Completion Date: April 2011
Primary Completion Date: April 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: LY450139
Participants received 60 milligrams (mg) LY450139 orally once daily for 2 weeks followed by 100 mg LY450139 orally once daily for 2 weeks, then 140 mg LY450139 orally once daily until Week 88.
Drug: LY450139
Administered orally once daily.
Other Name: Semagacestat
Placebo Comparator: Placebo
Participants received placebo orally once daily for the first 76 weeks. At the end of 76 weeks, participants in the placebo arm received LY450139 titrated up to 140 mg orally once daily until Week 88.
Drug: Placebo
Administered orally once daily.

  Eligibility

Ages Eligible for Study:   55 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Meets criteria for mild to moderate Alzheimer's disease (AD) with Mini-Mental State Examination score of 16 through 26 at visit 1
  • Modified Hachinski Ischemia Scale score of less than or equal to 4
  • Geriatric Depression Scale score of less than or equal to 6
  • A magnetic resonance imaging (MRI) or computerized tomography (CT) scan in the last 2 years with no findings inconsistent with a diagnosis of AD
  • If female, must be without menstruation for a least 12 consecutive months or have had both ovaries removed.

Exclusion Criteria:

  • Is not capable of swallowing whole oral medication
  • Has serious or unstable illnesses
  • Does not have a reliable caregiver
  • Chronic alcohol and/or drug abuse within the past 5 years
  • Has ever had a active vaccination for AD
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00762411

  Hide Study Locations
Locations
United States, Arizona
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Phoenix, Arizona, United States, 85004
United States, California
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Costa Mesa, California, United States, 92626
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La Jolla, California, United States, 92037
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Laguna Hills, California, United States, 92653
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Los Angeles, California, United States, 90036
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Oxnard, California, United States, 93030
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San Francisco, California, United States, 94109
United States, Florida
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Boca Raton, Florida, United States, 33431
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Hallandale Beach, Florida, United States, 33009
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Hollywood, Florida, United States, 33021
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Miami, Florida, United States, 33137
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Orlando, Florida, United States, 32806
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Tampa, Florida, United States, 33609
United States, Louisiana
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New Orleans, Louisiana, United States, 70131
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Shreveport, Louisiana, United States, 71104
United States, Mississippi
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Hattiesburg, Mississippi, United States, 39401
United States, Nebraska
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Omaha, Nebraska, United States, 68105
United States, New York
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Albany, New York, United States, 12205
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Manhasset, New York, United States, 11030
United States, North Carolina
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Durham, North Carolina, United States, 27710
United States, Oklahoma
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Oklahoma City, Oklahoma, United States, 73103
United States, Pennsylvania
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Philadelphia, Pennsylvania, United States, 19131
Brazil
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Rio De Janeiro, Brazil, 21020-130
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Salvador, Brazil, 40301500
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São Paulo, Brazil, 040024-002
Bulgaria
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Sofia, Bulgaria, 1527
Canada, Manitoba
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Winnipeg, Manitoba, Canada, R3N 0K6
Canada, New Brunswick
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Saint John, New Brunswick, Canada, E2L 3L6
Canada, Ontario
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London, Ontario, Canada, N6C 5J1
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Ottawa, Ontario, Canada, K1N 5C8
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Peterborough, Ontario, Canada, K9H2P4
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Toronto, Ontario, Canada, M3B2S7
Canada, Quebec
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Greenfield Park, Quebec, Canada, J4V 2J2
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Montreal, Quebec, Canada, H1T 2M4
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Verdun, Quebec, Canada, H4H 1R3
China
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Beijing, China, 100853
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Shanghai, China, 200025
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Xi'An, China, 710038
France
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Montpellier, France, 34295
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Paris, France, 75651
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Poitiers, France, 86021
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Strasbourg, France, 67091
Germany
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Berlin, Germany, 10629
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Frankfurt, Germany, 60528
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Hamburg, Germany, 22083
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Heidelberg, Germany, 69115
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Mannheim, Germany, 68165
Hungary
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Budapest, Hungary, H-1083
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Esztergom, Hungary, 2500
Italy
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Boggiovara, Italy, 41100
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Cassino, Italy, 03043
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Milano, Italy, 20122
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Parma, Italy, 43100
Japan
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Akita, Japan, 010-0874
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Fukuoka, Japan, 814-0180
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Hyogo, Japan, 655-0037
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Ibaraki, Japan, 305-8576
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Iwate, Japan, 020-8505
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Kanagawa, Japan, 251-0038
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Kumamoto, Japan, 861-8002
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Kyoto, Japan, 606-0851
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Nagasaki, Japan, 852-8108
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Osaka, Japan, 599-8263
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Saitama, Japan, 344-0036
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Tokyo, Japan, 113-8655
Korea, Republic of
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Seoul, Korea, Republic of, 139-707
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Suwon, Korea, Republic of, 443-721
Mexico
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Aguascalientes, Mexico, 20217
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Monterrey, Mexico, 64710
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Saltillo, Mexico, 25000
Romania
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Bucharest, Romania, 011241
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Timisoara, Romania, 300736
Russian Federation
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Ekaterinburg, Russian Federation, 620030
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Kazan, Russian Federation, 420101
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Saint Petersburg, Russian Federation, 190021
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Saratov, Russian Federation, 410028
Serbia
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Belgrade, Serbia, 11000
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Kragujevac, Serbia, 34000
Taiwan
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Changhua, Taiwan, 500
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Tainan, Taiwan, 70403
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Taipei, Taiwan, 111
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Tao-Yuan, Taiwan, 333
Turkey
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Eskisehir, Turkey, 26480
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Istanbul, Turkey, 34452
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Izmir, Turkey, 35340
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Samsun, Turkey
Ukraine
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Dnipropetrovsk, Ukraine, 49616
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Donetsk, Ukraine, 83037
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Kherson, Ukraine, 73488
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Kyiv, Ukraine, 04080
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Odesa, Ukraine, 65006
Sponsors and Collaborators
Eli Lilly and Company
Investigators
Study Director: Call 1-877-CTLILLY (1-877-285-4559 or 1-317-615-4559 Mon - Fri 9 AM - 5 PM eastern time (UTC/GMT - 5 hours, EST) Eli Lilly and Company
  More Information

No publications provided

Responsible Party: Eli Lilly and Company
ClinicalTrials.gov Identifier: NCT00762411     History of Changes
Other Study ID Numbers: 11271, H6L-MC-LFBC
Study First Received: September 26, 2008
Results First Received: November 6, 2013
Last Updated: September 22, 2014
Health Authority: United States: Food and Drug Administration

Keywords provided by Eli Lilly and Company:
Alzheimer's Disease

Additional relevant MeSH terms:
Alzheimer Disease
Brain Diseases
Central Nervous System Diseases
Delirium, Dementia, Amnestic, Cognitive Disorders
Dementia
Mental Disorders
Nervous System Diseases
Neurodegenerative Diseases
Tauopathies

ClinicalTrials.gov processed this record on November 25, 2014