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A Study of the Novel Drug Dimebon in Patients With Huntington's Disease — DIMOND  

Huntington's Disease Clinical Trial

Official title:
A Multi-Center, Phase 2 Randomized, Double-Blinded, Placebo-Controlled Study of Dimebon in Subjects With Huntington's Disease

Clinical Trial Summary

This study will evaluate the safety of 3 months of Dimebon dosing and the efficacy of Dimebon in improving cognitive, motor, and overall function in subjects with Huntington's Disease.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00497159
Study type Interventional
Source Medivation, Inc.
Contact
Status Completed
Phase Phase 2
Start date July 2007
Completion date June 2008
View Details
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