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Clinical Trial Summary

This will be a prospective, multi-center, randomized, double-blind, parallel group, placebo-controlled study, in participants with PD who are on a stable regimen of dopaminergic medication and have at least mild levodopa-induced dyskinesia. Eligible participants will be randomized to one of three treatment groups to receive adjunctive daily treatment with either safinamide 100 mg, safinamide 150 mg or placebo in a 1:1:1 ratio. Outcome will be assessed after 26 weeks of treatment.


Clinical Trial Description

Trial participation will be up to a maximum duration of 32 weeks and will comprise:

- Screening period (up to 4 weeks) for screening assessments;

- Two weeks titration period: participants randomized to the 100 mg study arm will receive 100 mg during Week 1 and throughout the rest of the study; participants randomized to the 150 mg study arm will receive 100 mg during Weeks 1 and 2 , and 150 mg from Week 3 and throughout the rest of the study; participants randomized to the placebo arm will receive identical placebo tablets.

- Twenty-four weeks maintenance period during which patients receive their randomized treatment as an adjunct to their standard anti-PD medications, which should remain unaltered. End of treatment evaluations will be performed at the end of Week 26 or at early discontinuation

- A telephone follow-up call will be performed 2 weeks after the end of treatment to assess adverse events and concomitant medications ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03987750
Study type Interventional
Source Zambon SpA
Contact
Status Withdrawn
Phase Phase 3
Start date October 2019
Completion date May 2021

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