Study of Idalopirdine in Patients With Mild - Moderate Alzheimer's Disease Treated With Donepezil

NCT ID: NCT01955161

Last Updated: 2017-09-19

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

View full results

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

933 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-10-31

Study Completion Date

2016-07-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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 30 mg/day or 60 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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Alzheimer's Disease

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Placebo

Placebo adjunct to 10 mg Donepezil

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DRUG

Once daily, matching placebo capsules, orally

Idalopirdine 30 mg

Idalopirdine adjunct to 10 mg Donepezil

Group Type EXPERIMENTAL

Idalopirdine

Intervention Type DRUG

Once daily, encapsulated tablets, orally

Idalopirdine 60 mg

Idalopirdine adjunct to 10 mg Donepezil

Group Type EXPERIMENTAL

Idalopirdine

Intervention Type DRUG

Once daily, encapsulated tablets, orally

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Placebo

Once daily, matching placebo capsules, orally

Intervention Type DRUG

Idalopirdine

Once daily, encapsulated tablets, orally

Intervention Type DRUG

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* The patient has a knowledgeable and reliable caregiver.
* The patient is an outpatient.
* The patient has probable AD.
* The patient has mild to moderate AD.
* Stable treatment with donepezil.
* The patient, if a woman, must have had her last natural menstruation ≥24 months prior to baseline, OR be surgically sterile.
* The patient, if a man, agrees to protocol-defined use of effective contraception if his female partner is of childbearing potential, OR must have been surgically sterilised prior to the screening visit.

Exclusion Criteria

* The patient has evidence of any clinically significant neurodegenerative disease, or other serious neurological disorders other than AD.
* The patient has a Diagnostic and Statistical Manual of Mental Disorders, 4th edition, Text Revision (DSM-IV-TR) Axis I disorder other than AD.
* The patient has evidence of clinically significant disease.
* The patient's donepezil therapy is likely to be interrupted or discontinued during the study.
* The patient is currently receiving memantine or has taken memantine within 2 months prior to screening.
Minimum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Otsuka Pharmaceutical Co., Ltd.

INDUSTRY

Sponsor Role collaborator

H. Lundbeck A/S

INDUSTRY

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Email contact via H. Lundbeck A/S

Role: STUDY_DIRECTOR

[email protected]

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

US027

Birmingham, Alabama, United States

Site Status

US012

Phoenix, Arizona, United States

Site Status

US024

Little Rock, Arkansas, United States

Site Status

US053

Glendale, California, United States

Site Status

US023

Imperial, California, United States

Site Status

US015

La Jolla, California, United States

Site Status

US045

Long Beach, California, United States

Site Status

US002

Los Angeles, California, United States

Site Status

US058

San Francisco, California, United States

Site Status

US018

Santa Ana, California, United States

Site Status

US060

Denver, Colorado, United States

Site Status

US042

Boca Raton, Florida, United States

Site Status

US021

Bradenton, Florida, United States

Site Status

US050

Brooksville, Florida, United States

Site Status

US019

Orlando, Florida, United States

Site Status

US038

Port Charlotte, Florida, United States

Site Status

US001

West Palm Beach, Florida, United States

Site Status

US020

Atlanta, Georgia, United States

Site Status

US048

Kailua, Hawaii, United States

Site Status

US030

Chicago, Illinois, United States

Site Status

US051

Joliet, Illinois, United States

Site Status

US040

Indianapolis, Indiana, United States

Site Status

US036

Freeport, Maine, United States

Site Status

US032

Newton, Massachusetts, United States

Site Status

US035

Kalamazoo, Michigan, United States

Site Status

US041

Flowood, Mississippi, United States

Site Status

US054

St Louis, Missouri, United States

Site Status

US046

Princeton, New Jersey, United States

Site Status

US028

Toms River, New Jersey, United States

Site Status

US044

Toms River, New Jersey, United States

Site Status

US049

Albany, New York, United States

Site Status

US010

Amherst, New York, United States

Site Status

US014

Manhasset, New York, United States

Site Status

US008

New York, New York, United States

Site Status

US029

New York, New York, United States

Site Status

US056

New York, New York, United States

Site Status

US037

Orangeburg, New York, United States

Site Status

US043

Staten Island, New York, United States

Site Status

US007

Centerville, Ohio, United States

Site Status

US006

Columbus, Ohio, United States

Site Status

US052

Edmond, Oklahoma, United States

Site Status

US026

Portland, Oregon, United States

Site Status

US057

Jenkintown, Pennsylvania, United States

Site Status

US047

Arlington, Virginia, United States

Site Status

US025

Madison, Wisconsin, United States

Site Status

US004

Milwaukee, Wisconsin, United States

Site Status

AR002

Buenos Aires, , Argentina

Site Status

AR003

Buenos Aires, , Argentina

Site Status

AR006

Buenos Aires, , Argentina

Site Status

AR007

Buenos Aires, , Argentina

Site Status

AR009

Córdoba, , Argentina

Site Status

AR004

Mar del Plata, , Argentina

Site Status

AR005

Mendoza, , Argentina

Site Status

AR008

Mendoza, , Argentina

Site Status

AR010

Rosario, , Argentina

Site Status

BE003

Bruges, , Belgium

Site Status

BE002

Brussels, , Belgium

Site Status

BE004

Brussels, , Belgium

Site Status

BE005

Leuven, , Belgium

Site Status

BE001

Roeselare, , Belgium

Site Status

BE006

Thuin, , Belgium

Site Status

BG005

Plovdiv, , Bulgaria

Site Status

BG001

Sofia, , Bulgaria

Site Status

BG002

Sofia, , Bulgaria

Site Status

BG003

Sofia, , Bulgaria

Site Status

BG004

Sofia, , Bulgaria

Site Status

BG006

Sofia, , Bulgaria

Site Status

BG007

Varna, , Bulgaria

Site Status

CA002

Gatineau, , Canada

Site Status

CA006

London, , Canada

Site Status

CA008

Newmarket, , Canada

Site Status

CA001

Toronto, , Canada

Site Status

CA004

Toronto, , Canada

Site Status

CL004

Antofagasta, , Chile

Site Status

CL002

Santiago, , Chile

Site Status

CL003

Santiago, , Chile

Site Status

CL005

Santiago, , Chile

Site Status

CL001

Valdivia, , Chile

Site Status

CZ006

Brno, , Czechia

Site Status

CZ007

Kutná Hora, , Czechia

Site Status

CZ004

Pardubice, , Czechia

Site Status

CZ001

Prague, , Czechia

Site Status

CZ002

Prague, , Czechia

Site Status

CZ003

Prague, , Czechia

Site Status

CZ005

Rychnov nad Kněžnou, , Czechia

Site Status

DK003

Aarhus N, , Denmark

Site Status

DK001

Copenhagen, , Denmark

Site Status

DK002

Odense C, , Denmark

Site Status

FR006

Besançon, , France

Site Status

FR008

Limoges Cedex1, , France

Site Status

FR003

Nantes, , France

Site Status

FR001

Paris, , France

Site Status

FR005

Paris, , France

Site Status

FR004

Saint-Etienne, , France

Site Status

FR002

Toulouse, , France

Site Status

DE002

Berlin, , Germany

Site Status

DE006

Ellwangen, , Germany

Site Status

DE010

Günzburg, , Germany

Site Status

DE005

Hanover, , Germany

Site Status

DE007

Heidelberg, , Germany

Site Status

DE009

München, , Germany

Site Status

DE008

Ulm, , Germany

Site Status

DE004

Unterhaching, , Germany

Site Status

IT004

Ancona, , Italy

Site Status

IT006

Brescia, , Italy

Site Status

IT002

Florence, , Italy

Site Status

IT005

Genoa, , Italy

Site Status

IT003

Lamezia Terme, , Italy

Site Status

IT001

Milan, , Italy

Site Status

IT007

Palermo, , Italy

Site Status

PL004

Gliwice, , Poland

Site Status

PL007

Katowice, , Poland

Site Status

PL005

Poznan, , Poland

Site Status

PL006

Sopot, , Poland

Site Status

PL002

Szczecin, , Poland

Site Status

PL003

Warsaw, , Poland

Site Status

PL008

Wroclaw, , Poland

Site Status

RO002

Bucharest, , Romania

Site Status

RO001

Târgu Mureş, , Romania

Site Status

ZA003

Bloemfontein, , South Africa

Site Status

ZA006

Cape Town, , South Africa

Site Status

ZA007

Cape Town, , South Africa

Site Status

ZA004

George, , South Africa

Site Status

ZA005

Port Elizabeth, , South Africa

Site Status

ZA001

Pretoria, , South Africa

Site Status

ZA002

Rosebank, , South Africa

Site Status

ES002

Alicante, , Spain

Site Status

ES006

Barcelona, , Spain

Site Status

ES001

Donostia / San Sebastian, , Spain

Site Status

ES005

Manresa, , Spain

Site Status

ES004

Salamanca, , Spain

Site Status

ES003

Santiago de Compostela, , Spain

Site Status

UA008

Dnipropetrovsk, , Ukraine

Site Status

UA006

Kherson,Vil. Stepanivka, , Ukraine

Site Status

UA005

Kyiv, , Ukraine

Site Status

UA007

Kyiv, , Ukraine

Site Status

UA001

Lviv, , Ukraine

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States Argentina Belgium Bulgaria Canada Chile Czechia Denmark France Germany Italy Poland Romania South Africa Spain Ukraine

References

Explore related publications, articles, or registry entries linked to this study.

Ballard C, Atri A, Boneva N, Cummings JL, Frolich L, Molinuevo JL, Tariot PN, Raket LL. Enrichment factors for clinical trials in mild-to-moderate Alzheimer's disease. Alzheimers Dement (N Y). 2019 May 20;5:164-174. doi: 10.1016/j.trci.2019.04.001. eCollection 2019.

Reference Type DERIVED
PMID: 31193334 (View on PubMed)

Cummings JL, Atri A, Ballard C, Boneva N, Frolich L, Molinuevo JL, Raket LL, Tariot PN. Insights into globalization: comparison of patient characteristics and disease progression among geographic regions in a multinational Alzheimer's disease clinical program. Alzheimers Res Ther. 2018 Nov 24;10(1):116. doi: 10.1186/s13195-018-0443-2.

Reference Type DERIVED
PMID: 30474567 (View on PubMed)

Atri A, Frolich L, Ballard C, Tariot PN, Molinuevo JL, Boneva N, Windfeld K, Raket LL, Cummings JL. Effect of Idalopirdine as Adjunct to Cholinesterase Inhibitors on Change in Cognition in Patients With Alzheimer Disease: Three Randomized Clinical Trials. JAMA. 2018 Jan 9;319(2):130-142. doi: 10.1001/jama.2017.20373.

Reference Type DERIVED
PMID: 29318278 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

2012-004763-45

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

14861A

Identifier Type: -

Identifier Source: org_study_id