Safety/Efficacy Study of Levodopa-Carbidopa Intestinal Gel in Parkinson's Subjects
Public ClinicalTrials.gov record NCT00360568. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
Open-Label, 12-Month Safety and Efficacy Study of Levodopa - Carbidopa Intestinal Gel in Levodopa-Responsive Parkinson's Disease Subjects
Study identification
- NCT ID
- NCT00360568
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 3
- Lead sponsor
- AbbVie (prior sponsor, Abbott)
- Industry
- Enrollment
- 62 participants
Conditions and interventions
Interventions
- Levodopa-carbidopa intestinal gel Drug
- CADD-Legacy® 1400 ambulatory infusion pump Device
- PEG tube Device
- J-tube Device
Drug · Device
Eligibility (public fields only)
- Age range
- 30 Years and older
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- May 31, 2009
- Primary completion
- Sep 30, 2012
- Completion
- Sep 30, 2012
- Last update posted
- Jan 15, 2015
2009 – 2012
United States locations
- U.S. sites
- 16
- U.S. states
- 11
- U.S. cities
- 16
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Site Reference ID/Investigator# 45869 | Birmingham | Alabama | 35222 | — |
| Site Reference ID/Investigator# 45834 | Fountain Valley | California | 92708 | — |
| Site Reference ID/Investigator# 45854 | Los Angeles | California | 90033 | — |
| Site Reference ID/Investigator# 45856 | Oceanside | California | 92056 | — |
| Site Reference ID/Investigator# 45859 | Washington D.C. | District of Columbia | 20007 | — |
| Site Reference ID/Investigator# 45857 | Bradenton | Florida | 34205 | — |
| Site Reference ID/Investigator# 45863 | Gainesville | Florida | 32610 | — |
| Site Reference ID/Investigator# 45836 | Port Charlotte | Florida | 33890 | — |
| Site Reference ID/Investigator# 45874 | Chicago | Illinois | 60611 | — |
| Site Reference ID/Investigator# 45868 | Lexington | Kentucky | 40536 | — |
| Site Reference ID/Investigator# 45862 | Baltimore | Maryland | 21201 | — |
| Site Reference ID/Investigator# 45861 | St Louis | Missouri | 63110 | — |
| Site Reference ID/Investigator# 45873 | New York | New York | 10032 | — |
| Site Reference ID/Investigator# 45878 | Cincinnati | Ohio | 45267 | — |
| Site Reference ID/Investigator# 45850 | Cleveland | Ohio | 44195-0001 | — |
| Site Reference ID/Investigator# 45887 | Burlington | Vermont | 05401 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
Non-U.S. locations
This page focuses on the U.S. directory. The official record also lists 6 non-U.S. sites.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT00360568, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Jan 15, 2015 · Synced Jul 24, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT00360568 live on ClinicalTrials.gov.