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Completed Phase 3 Interventional

A Safety and Efficacy Study of Oral Dimebon in Patients With Mild-To-Moderate Alzheimer's Disease

ClinicalTrials.gov ID: NCT00675623

Public ClinicalTrials.gov record NCT00675623. 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 Nov 5, 2026, 1:02 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Global Phase 3, Double-Blind, Placebo-Controlled Safety and Efficacy Study of Oral Dimebon in Patients With Mild-to-Moderate Alzheimer's Disease (CONNECTION)

Brief summary

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

The Connection Study is a six-month confirmatory Phase 3 study to determine the safety and efficacy of Dimebon in the treatment of mild-to-moderate Alzheimer's disease (AD).

Study identification

NCT ID
NCT00675623
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Medivation, Inc.
Industry
Enrollment
598 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
May 2008 (Type not available)
Primary completion
Dec 2009 (Actual)
Completion
Not listed
Last update posted
Sep 27, 2016

Started 2008

United States locations

U.S. sites
28
U.S. states
15
U.S. cities
28
Facility City State ZIP Site status
Not listed Phoenix Arizona 85004 —
Not listed Costa Mesa California — —
Not listed Fresno California 93720 —
Not listed Rancho Mirage California — —
Not listed Hamden Connecticut — —
Not listed New Haven Connecticut — —
Not listed Norwalk Connecticut — —
Not listed Hallandale Florida 33009 —
Not listed Hialeah Florida — —
Not listed Miami Florida 33137 —
Not listed North Miami Florida 33161 —
Not listed Sunrise Florida 33351 —
Not listed West Palm Beach Florida 33407 —
Not listed Indianapolis Indiana 46260 —
Not listed Paducah Kentucky 42003 —
Not listed Newton Massachusetts 02459 —
Not listed Ann Arbor Michigan — —
Not listed St Louis Missouri 63044 —
Not listed Brooklyn New York — —
Not listed Cedarhurst New York 11516 —
Not listed New York New York — —
Not listed Rochester New York 14620 —
Not listed Staten Island New York — —
Not listed Morganton North Carolina 28655 —
Not listed Centerville Ohio — —
Not listed Norristown Pennsylvania — —
Not listed Austin Texas — —
Not listed Middleton Wisconsin 53562 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00675623, 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 Sep 27, 2016 · Synced Nov 5, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00675623 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →