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Clinical Trial Summary

This study is designed to evaluate the safety and efficacy of dipraglurant in PD patients with dyskinesia (randomized 1:1 to receive active or placebo) for 12 weeks (1 week at 150 mg per day and 11 weeks at 300 mg per day). The primary efficacy assessment will be based on the Unified Dyskinesia Rating Scale (UDysRS). Patients who complete the 12-week blinded treatment period may have the option to roll into an open-label safety extension study for an additional 12-month treatment period.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04857359
Study type Interventional
Source Addex Pharma S.A.
Contact Study Director
Phone 877-409-1775
Email [email protected]
Status Not yet recruiting
Phase Phase 2/Phase 3
Start date April 2021
Completion date April 2023

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