Adding Atomoxetine To Standard Medication Treatment In Patients With Alzheimer's Disease

PHASE2/PHASE3CompletedINTERVENTIONAL
Enrollment

124

Participants

Timeline

Start Date

October 31, 2003

Study Completion Date

January 31, 2006

Conditions
Alzheimer Disease
Interventions
DRUG

atomoxetine hydrochloride

DRUG

placebo

Trial Locations (3)

Unknown

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician, Sherman Oaks

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician, Rochester

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician, Wichita Falls

All Listed Sponsors
lead

Eli Lilly and Company

INDUSTRY

NCT00191009 - Adding Atomoxetine To Standard Medication Treatment In Patients With Alzheimer's Disease | Biotech Hunter | Biotech Hunter