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Completed Phase 3 Interventional

A Safety and Efficacy Study of Dimebon in Patients With Huntington Disease

ClinicalTrials.gov ID: NCT00920946

Public ClinicalTrials.gov record NCT00920946. 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 Sep 24, 2026, 6:45 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 Phase 3, Randomized, Double-Blind, Placebo-Controlled Safety and Efficacy Study of Dimebon in Patients With Mile-to-Moderate Huntington Disease

Brief summary

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

The purpose of this study is to determine if Dimebon is safe and effective for the treatment of cognitive impairment in Huntington disease.

Study identification

NCT ID
NCT00920946
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Medivation, Inc.
Industry
Enrollment
403 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
30 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
Jun 30, 2009
Primary completion
Jun 30, 2011
Completion
Not listed
Last update posted
Oct 11, 2016

Started 2009

United States locations

U.S. sites
24
U.S. states
15
U.S. cities
24
Facility City State ZIP Site status
Not listed Scottsdale Arizona 85259 —
Not listed Davis California 95616 —
Not listed Irvine California 92697 —
Not listed La Jolla California 92161 —
Not listed San Francisco California 94143 —
Not listed Gainsville Florida 32610 —
Not listed Miami Florida 33136 —
Not listed Boise Idaho 83702 —
Not listed Indianapolis Indiana 46202 —
Not listed Kansas City Kansas 66160 —
Not listed Wichita Kansas 67206 —
Not listed Charlestown Massachusetts 02129 —
Not listed Golden Valley Minnesota 55427 —
Not listed St Louis Missouri 63110 —
Not listed New York New York 10032 —
Not listed Rochester New York 14620 —
Not listed Durham North Carolina 27705 —
Not listed Winstom-Salem North Carolina 27157 —
Not listed Cleveland Ohio 44195 —
Not listed Columbus Ohio 43210 —
Not listed Portland Oregon 97201 —
Not listed Philadelphia Pennsylvania 19107 —
Not listed Pittsburgh Pennsylvania 15213 —
Not listed Milwaukee Wisconsin 53226 —

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 13 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00920946, 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 Oct 11, 2016 · Synced Sep 24, 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 protocol, eligibility criteria, and contact information for NCT00920946 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →