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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 Oct 28, 2026, 11:36 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 Study of Idalopirdine in Patients With Mild - Moderate Alzheimer's Disease Treated With an Acetylcholinesterase Inhibitor

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

To establish efficacy of idalopirdine as adjunctive therapy to acetylcholinesterase inhibitors (AChEIs) for symptomatic treatment of patients with mild-moderate Alzheimer's disease (AD).

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

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
Mar 2014 (Type not available)
Primary completion
Jan 2017 (Actual)
Completion
Jan 2017 (Actual)
Last update posted
Feb 7, 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 7, 2018 · Synced Oct 28, 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 public registry record, listed eligibility criteria, and available contact information for NCT02006654 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →