Parkinson's Disease (PD) Clinical Trial
Official title:
A 52-Week, Open-label, Single-arm Study to Evaluate the Safety and Tolerability of 24-hour Daily Exposure of Continuous Subcutaneous Infusion of ABBV-951 in Subjects With Parkinson's Disease
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.
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| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
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||
| Completed |
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Phase 1 | |
| Completed |
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Phase 1 | |
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Phase 2 | |
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| Completed |
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Phase 1 | |
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Phase 3 |