drugset / Trial / NCT00387270

Safety Study of the Novel Drug Dimebon to Treat Patients With Huntington's Disease

NCT00387270

Phase 1/2 Completed 9 enrolled Medivation, Inc. Huntington Study Group · collab
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This study is being conducted to determine the safety and tolerability of Dimebon in people with Huntington's disease after short-term exposure (one week) and after longer exposure (three months). Also, the study will assess whether or not there is an effect of Dimebon on the symptoms of Huntington's disease, including cognitive (thinking abilities), motor (movement), behavior, and overall functioning.

Timeline

Start
2006-10
Primary completion
2007-03
Completion
2007-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Latrepirdine Small molecule 10 mg
Subject Latrepirdine Small molecule 20 mg

Indications