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Clinical Trial Summary

This study will evaluate the efficacy and safety of pridopidine 45mg twice daily (BID) in patients with early stage manifest Huntington Disease (HD).

Clinical Trial Description

This is a phase 3, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of pridopidine 45 mg BID in patients with early stage HD. Eligible patients who completed the Main Study (65 to 78 weeks) will have the option to enroll into an open-label extension. ;

Study Design

Related Conditions & MeSH terms

NCT number NCT04556656
Study type Interventional
Source Prilenia
Status Active, not recruiting
Phase Phase 3
Start date October 16, 2020
Completion date March 14, 2024

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