Last updated on July 2019

Study of AGB101 in Mild Cognitive Impairment Due to Alzheimer's Disease

Brief description of study

The primary objective of the study is to evaluate the efficacy of AGB101 on slowing cognitive and functional impairment as measured by changes in the Clinical Dementia Rating-Sum of Boxes (CDR-SB) score as compared with placebo in participants with mild cognitive impairment due to Alzheimer's Disease (MCI due to AD) also known as prodromal AD. Participants will be randomized to receive placebo or AGB101 (220 mg), once daily for 78 weeks. Secondary objectives are to assess the effect of AGB101 compared with placebo on clinical progression as measured by Mini-Mental State Examination (MMSE) and Functional Activities Questionnaire (FAQ).

Clinical Study Identifier: NCT03486938

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Excell Research Inc

Oceanside, CA United States
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Waterbury, CT United States
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Palmetto Bay, FL United States
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Sarasota, FL United States
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Decatur, GA United States
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Clinical Trials of Texas, Inc

San Antonio, TX United States
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Senior Clinical Trials, Inc.

Laguna Hills, CA United States
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Care Access Research, Santa Clarita

Santa Clarita, CA United States
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MD Clinical

Hallandale Beach, FL United States
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Miami Jewish Health

Miami, FL United States
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Great Lakes Clinical Trials

Chicago, IL United States
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Richmond Behavioral Associates

Staten Island, NY United States
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Bioclinica Research

Orlando, FL United States
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Recruitment Status: Open

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