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Clinical Trial Summary

This open-label study is designed to assess the long-term safety and tolerability of dipraglurant in PD patients for up to 52 weeks (at doses of 150-300 mg per day) for patients that have completed an Addex sponsored double-blind clinical trial of dipraglurant.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05116813
Study type Interventional
Source Addex Pharma S.A.
Contact Study Director
Phone 877-409-1775
Email addex@druginfo.com
Status Recruiting
Phase Phase 2/Phase 3
Start date October 25, 2021
Completion date December 2023

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