Huntington's Disease Clinical Trial
Official title:
A Multicenter, Multinational, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of Laquinimod (0.5, 1.0 and 1.5 mg/Day) as Treatment in Patients With Huntington's Disease
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).
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Status | Clinical Trial | Phase | |
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Recruiting |
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Phase 1/Phase 2 | |
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Phase 2 | |
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Phase 2 | |
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Phase 1 | |
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N/A | |
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Phase 2 | |
Completed |
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Phase 3 | |
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Completed |
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Phase 1/Phase 2 | |
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Phase 2 | |
Not yet recruiting |
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N/A | |
Active, not recruiting |
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Phase 2/Phase 3 | |
Completed |
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Phase 1 | |
Completed |
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Phase 1/Phase 2 | |
Completed |
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Phase 2 | |
Completed |
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Phase 1/Phase 2 |