Clinical trial
Safety/Efficacy Study of Levodopa-Carbidopa Intestinal Gel in Parkinson's…
NCT00360568 · AbbVie (prior sponsor, Abbott), Industry · Completed
Key facts
| NCT number | NCT00360568 |
|---|---|
| Title | Safety/Efficacy Study of Levodopa-Carbidopa Intestinal Gel in Parkinson's Subjects |
| Official title | Open-Label, 12-Month Safety and Efficacy Study of Levodopa - Carbidopa Intestinal Gel in Levodopa-Responsive Parkinson's Disease Subjects |
| Lead sponsor | AbbVie (prior sponsor, Abbott), Industry |
| Collaborators | Quintiles, Inc. Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Dyskinesias, Parkinson's Disease, Severe Motor Fluctuations |
| Intervention type | Device, Drug |
| Interventions | Levodopa-carbidopa intestinal gel, CADD-Legacy® 1400 ambulatory infusion pump, PEG tube, J-tube |
| Enrollment | 62 |
| Start date | Jun 1, 2009 |
| Primary completion | Oct 1, 2012 |
| Completion | Oct 1, 2012 |
| First posted | Aug 4, 2006 |
| Last update posted | Jan 16, 2015 |
| Countries | Germany, New Zealand, United States |
At a glance
- 10–99 Study sites
- Yes Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: