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Clinical Trial Summary

This study assesses the safety, tolerability, pharmacokinetics and efficacy of SAGE-217 in 29 participants with moderate to severe Parkinson's Disease.


Clinical Trial Description

Part A of the study is an open-label design with dosing of Levodopa for 3 days followed by SAGE-217 for 4 days. Part B of the study is an open-label design with evening dosing of SAGE-217 for 7 days as an adjunct to antiparkinsonian agent(s). This study was previously posted by Sage Therapeutics. In November 2023, sponsorship of the trial was transferred to Biogen. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03000569
Study type Interventional
Source Biogen
Contact
Status Completed
Phase Phase 2
Start date November 30, 2016
Completion date September 11, 2017

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