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Clinical Trial Summary

The purpose of this study is to evaluate whether the DopaFuse System can reduce the fluctuation of plasma levodopa levels compared to participants' standard intermittent doses of oral LD/CD tablets (background treatment). It will also assess whether the system is safe, well tolerated, and can relieve motor symptoms.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04778176
Study type Interventional
Source SynAgile Corporation
Contact
Status Completed
Phase Phase 2
Start date June 16, 2021
Completion date August 2, 2022

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