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Clinical Trial Summary

The purpose of this study was to assess the safety and tolerability of ABBV-951 (Foslevodopa/Foscarbidopa) in participants with Parkinson's disease (PD). This was a single-arm study with preplanned analyses conducted by dose subgroup (Low Dose or High Dose) based on the modal total daily dose (most frequent dose) over the treatment period.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03781167
Study type Interventional
Source AbbVie
Contact
Status Completed
Phase Phase 3
Start date April 29, 2019
Completion date August 17, 2022

See also
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