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Completed Phase 3 Interventional Results available

Idalopirdine in Patients With Mild-moderate Alzheimer's Disease Treated With Donepezil

ClinicalTrials.gov ID: NCT02006641

Public ClinicalTrials.gov record NCT02006641. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 10, 2026, 11:27 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Randomised, Double-blind, Parallel-group, Placebo-controlled, Fixed-dose Study of Idalopirdine in Patients With Mild-moderate Alzheimer's Disease Treated With Donepezil

Study identification

NCT ID
NCT02006641
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
H. Lundbeck A/S
Industry
Enrollment
858 participants

Conditions and interventions

Interventions

  • Idalopirdine Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
50 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 31, 2014
Primary completion
Nov 30, 2016
Completion
Nov 30, 2016
Last update posted
Feb 19, 2018

2014 – 2016

United States locations

U.S. sites
48
U.S. states
20
U.S. cities
46
Facility City State ZIP Site status
US338 Phoenix Arizona
US342 Fayetteville Arkansas
US322 Anaheim California
US305 Carson California
US346 Costa Mesa California
US327 Fullerton California
US315 Lomita California
US351 Oceanside California
US307 Redlands California
US301 Santa Rosa California
US337 New London Connecticut
US332 Stamford Connecticut
US308 Delray Beach Florida
US320 Hallandale Florida
US347 Hialeah Florida
US340 Lake Worth Florida
US303 Miami Florida
US313 Miami Florida
US335 Naples Florida
US345 Orange City Florida
US309 Palm Beach Gardens Florida
US302 Sunrise Florida
US304 Atlanta Georgia
US360 Augusta Georgia
US318 Decatur Georgia
US334 Lake Charles Louisiana
US350 Belmont Massachusetts
US344 Boston Massachusetts
US310 Saint Paul Minnesota
US321 Hattiesburg Mississippi
US330 Creve Coeur Missouri
US339 Paterson New Jersey
US312 Staten Island New York
US316 Charlotte North Carolina
US336 Winston-Salem North Carolina
US323 Cincinnati Ohio
US349 Cleveland Ohio
US306 Columbus Ohio
US352 Lakewood Ohio
US333 Oklahoma City Oklahoma
US314 Allentown Pennsylvania
US324 Pittsburgh Pennsylvania
US341 Pittsburgh Pennsylvania
US325 Reading Pennsylvania
US319 Port Royal South Carolina
US356 Cordova Tennessee
US343 Fort Worth Texas
US354 Houston Texas

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 114 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02006641, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 19, 2018 · Synced May 10, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02006641 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →