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Completed Phase 3 Interventional Results available

Study of Idalopirdine in Patients With Mild - Moderate Alzheimer's Disease Treated With an Acetylcholinesterase Inhibitor

ClinicalTrials.gov ID: NCT02006654

Public ClinicalTrials.gov record NCT02006654. 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 7, 2026, 11:34 AM 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 Study of Idalopirdine in Patients With Mild - Moderate Alzheimer's Disease Treated With an Acetylcholinesterase Inhibitor

Study identification

NCT ID
NCT02006654
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
H. Lundbeck A/S
Industry
Enrollment
734 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
Feb 28, 2014
Primary completion
Dec 31, 2016
Completion
Dec 31, 2016
Last update posted
Feb 6, 2018

2014 – 2017

United States locations

U.S. sites
26
U.S. states
15
U.S. cities
26
Facility City State ZIP Site status
US612 Mesa Arizona
US625 Bellflower California
US626 Costa Mesa California
US604 Oxnard California
US627 Santa Ana California
US609 Danbury Connecticut
US614 Norwalk Connecticut
US608 Deerfield Beach Florida
US616 Hialeah Florida
US620 Miami Florida
US603 North Palm Beach Florida
US631 Port Charlotte Florida
US622 Elk Grove Village Illinois
US611 Elkhart Indiana
US606 Prairie Village Kansas
US601 Farmington Hills Michigan
US607 St Louis Missouri
US613 Lawrenceville New Jersey
US635 Paterson New Jersey
US630 Toms River New Jersey
US621 Albany New York
US632 Staten Island New York
US633 Charlotte North Carolina
US623 Oklahoma City Oklahoma
US618 Norristown Pennsylvania
US619 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 81 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02006654, 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 6, 2018 · Synced May 7, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02006654 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →