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Clinical Trial Summary

This study is designed to assess the safety and tolerability of dipraglurant in patients with blepharospasm (BSP) (randomized 1:1:1 to receive dipraglurant 50 mg, 100 mg or placebo) and explore the efficacy of 50 mg and 100 mg immediate release tablets (versus placebo) on the severity and frequency of BSP signs and symptoms using objective measures, clinical ratings and patient reported outcomes.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05027997
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
Start date August 2021
Completion date December 2021

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