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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 Jul 22, 2026, 6:34 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

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)

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

  • Dimebon 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
Apr 30, 2008
Primary completion
Nov 30, 2009
Completion
Not listed
Last update posted
Sep 26, 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 26, 2016 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00675623 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →