A Placebo-Controlled, Double-Blind, Parallel-Group, 18-Month Study With an Open-Label Extension Phase to Confirm Safety and Efficacy of BAN2401 in Subjects With Early Alzheimer’s Disease

  • STATUS
    Not Recruiting
Updated on 25 September 2022
dementia
mini-mental state examination
amyloid
mental state examination
memantine
acetylcholinesterase
acetylcholinesterase inhibitor

Summary

This study will be conducted to evaluate the efficacy of BAN2401 in participants with early Alzheimer's disease (EAD) by determining the superiority of BAN2401 compared with placebo on the change from baseline in the Clinical Dementia Rating-Sum of Boxes (CDR-SB) at 18 months of treatment in the Core Study.
This study will also evaluate the long-term safety and tolerability of BAN2401 in participants with EAD in the Extension Phase and whether the long-term effects of BAN2401 as measured by the CDR-SB at the end of the Core Study is maintained over time in the Extension Phase.
 

Description

    - Participants will receive all study related medical care - Diagnostic tests for Alzheimer's Disease for free - Study medication - Participants will be compensated for their time and travel.

Details
Condition Alzheimer's Disease, Alzheimer's Disease
Clinical Study IdentifierTX228684
Last Modified on25 September 2022

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