Dose-Finding Study To Evaluate Safety, Tolerability, and Efficacy of E2609 in Participants With Mild Cognitive Impairment Due to Alzheimer's Disease (Prodromal Alzheimer's Disease) and Mild to Moderate Dementia Due to Alzheimer's Disease

PHASE2TerminatedINTERVENTIONAL
Enrollment

70

Participants

Timeline

Start Date

November 26, 2014

Primary Completion Date

December 20, 2019

Study Completion Date

December 20, 2019

Conditions
Alzheimer DiseaseDementia, Alzheimer Type
Interventions
DRUG

E2609

Each participant will receive 2 tablets, which when combined will make up the required doses of E2609 or placebo, to be administered orally once per day (QD) with food.

DRUG

Placebo

Each participant will receive 2 tablets, which when combined will make up the required doses of E2609 or placebo, to be administered orally once per day (QD) with food.

Trial Locations (21)

Unknown

Bellflower

Costa Mesa

Glendale

Irvine

Aventura

Boca Raton

Brooksville

Lake Worth

Orlando

Port Charlotte

Atlanta

Savannah

Wichita

Kalamazoo

Mount Arlington

Scotch Plains

Charlotte

Dayton

Port Royal

Dallas

San Antonio

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Biogen

INDUSTRY

lead

Eisai Inc.

INDUSTRY