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Clinical Trial Summary

The primary objective of this study is to assess the efficacy of laquinimod as treatment in participants with HD after 52 weeks using the Unified Huntington's Disease Rating Scale Total Motor Score (UHDRS-TMS or TMS).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02215616
Study type Interventional
Source Teva Pharmaceutical Industries
Contact
Status Completed
Phase Phase 2
Start date October 28, 2014
Completion date June 19, 2018

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