Extension Study To Evaluate Safety And Tolerability Of 24-Hour Daily Exposure Of Continuous Subcutaneous Infusion of ABBV-951 In Adult Participants With Parkinson's Disease
Public ClinicalTrials.gov record NCT04379050. 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
An Open-label Extension of Study M15-741 to Evaluate the Safety and Tolerability of 24-hour Daily Exposure of Continuous Subcutaneous Infusion of ABBV-951 in Subjects With Parkinson's Disease
Study identification
- NCT ID
- NCT04379050
- Recruitment status
- Active, not recruiting
- Study type
- Interventional
- Phase
- Phase 3
- Lead sponsor
- AbbVie
- Industry
- Enrollment
- 130 participants
Conditions and interventions
Conditions
Interventions
- ABBV-951 Drug
Drug
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
- Jun 7, 2020
- Primary completion
- Mar 31, 2026
- Completion
- Mar 31, 2026
- Last update posted
- Aug 4, 2025
2020 – 2026
United States locations
- U.S. sites
- 15
- U.S. states
- 12
- U.S. cities
- 15
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| University of Alabama at Birmingham - Main /ID# 215597 | Birmingham | Alabama | 35233 | — |
| Banner Sun Health Research Institute /ID# 215579 | Sun City | Arizona | 85351 | — |
| University of Colorado Hospital /ID# 215625 | Aurora | Colorado | 80045 | — |
| Parkinson's Disease and Movement Disorders Center of Boca Raton /ID# 215412 | Boca Raton | Florida | 33486 | — |
| Indiana Clinical Research Cent /ID# 216490 | Indianapolis | Indiana | 46202 | — |
| Univ Kansas Med Ctr /ID# 215624 | Kansas City | Kansas | 66160 | — |
| Washington University-School of Medicine /ID# 215472 | St Louis | Missouri | 63110 | — |
| Dartmouth-Hitchcock Medical Center /ID# 216834 | Lebanon | New Hampshire | 03756 | — |
| M3 Wake Research Inc. /ID# 215596 | Raleigh | North Carolina | 27612-8106 | — |
| Legacy Medical Group - Neurology /ID# 215536 | Portland | Oregon | 97232-2003 | — |
| Baylor College of Medicine /ID# 215401 | Houston | Texas | 77030 | — |
| Central Texas Neurology Consul /ID# 217013 | Round Rock | Texas | 78681 | — |
| Univ Texas HSC San Antonio /ID# 215400 | San Antonio | Texas | 78229-3901 | — |
| Booth Gardner Parkinson's Care Center /ID# 215535 | Kirkland | Washington | 98034-3029 | — |
| Inland Northwest Research /ID# 215533 | Spokane | Washington | 99202-1342 | — |
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 36 non-U.S. sites.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT04379050, 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 Aug 4, 2025 · Synced Apr 23, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT04379050 live on ClinicalTrials.gov.