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Randomised, Double-blind, Parallel-group, Placebo-controlled, Fixed-dose Study of Idalopirdine in Patients With Mild-moderate Alzheimer's Disease Treated With Donepezil
To establish efficacy of Idalopirdine as adjunctive therapy to donepezil for symptomatic treatment of patients with mild-to-moderate Alzheimer's disease (AD).
The study consisted of a screening period (up to 2-week period from screening to randomization), a 24-week double-blind treatment period with placebo or idalopirdine 10 mg/day or 30 mg/day as adjunctive therapy to donepezil 10 mg/day, and a 4-week safety follow-up period following study completion or withdrawal from treatment.
Age
50 - No limit years
Sex
ALL
Healthy Volunteers
No
US338
Phoenix, Arizona, United States
US342
Fayetteville, Arkansas, United States
US322
Anaheim, California, United States
US305
Carson, California, United States
US346
Costa Mesa, California, United States
US327
Fullerton, California, United States
US315
Lomita, California, United States
US351
Oceanside, California, United States
US307
Redlands, California, United States
US301
Santa Rosa, California, United States
Start Date
February 1, 2014
Primary Completion Date
December 1, 2016
Completion Date
December 1, 2016
Last Updated
February 20, 2018
858
ACTUAL participants
Placebo
DRUG
Idalopirdine
DRUG
Lead Sponsor
H. Lundbeck A/S
Collaborators
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07033494