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Safety and Tolerability of Tozadenant as Adjunctive Therapy in Levodopa-Treated Patients With Parkinson's Disease.

Idiopathic Parkinson Disease Clinical Trial

Official title:
A Multicenter, Open-Label Study to Evaluate the Safety and Tolerability of Tozadenant as Adjunctive Therapy in Levodopa-Treated Patients With Parkinson's Disease Experiencing End of Dose "Wearing-Off"

Clinical Trial Summary

Phase 3, international, multicenter, open-label 12 month safety study.

Clinical Trial Description

Each patient will participate for up to 52 weeks, which includes a Screening Period, followed by a Baseline Visit and open-label treatment for 1 year with a safety Follow-up 4 weeks after the last treatment.

- Screening Period: up to 6 weeks.

- Open-Label Treatment Period: 52 weeks (1 year)

- Post-Treatment Safety Follow Up: 4 weeks. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03051607
Study type Interventional
Source Biotie Therapies Inc.
Contact
Status Terminated
Phase Phase 3
Start date April 10, 2017
Completion date January 16, 2018
View Details
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