Clinical Trial

A Study to Assess Change in Disease Symptoms in Adult Participants With Advanced Parkinson Disease Using Subcutaneous Foslevodopa/Foscarbidopa in Belgium

Study acronym: ProParkB
Recruiting
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Summary
Parkinson's disease (PD) is a neurological condition, which affects the brain. PD gets worse over time, but how quickly it progresses varies a lot from person to person. Some symptoms of PD are tremors, stiffness, and slowness of movement. This study will assess how effective Foslevodopa/Foscarbidopa is in treating adult participants with advanced Parkinson Disease under routine clinical practice in Belgium. Foslevodopa/Foscarbidopa is an approved drug for the treatment of Parkinson's Disease. Approximately 120 adult participants who are prescribed Foslevodopa/Foscarbidopa by their doctors will be enrolled at 15 sites across Belgium. Participants will receive Foslevodopa/Foscarbidopa subcutaneous infusion as prescribed by their physician. Participants will be followed for up to 18 months. There is expected to be no additional burden for participants in this trial. Participants will attend regular visits during the study at a hospital or clinic according to their routine clinical practice.
Protocol Amendment History 4 changes
critical Recruitment opened 2026-04-08
notable Trial sites expanded: 0 -> 10 locations 2026-04-08
notable Primary completion pushed: 2027-12 -> 2028-09 2026-04-08
minor Completion pushed: 2027-12 -> 2028-09 2026-04-08
Trial Details
NCT Number NCT07382440
Lead Sponsor AbbVie
Conditions Parkinson's Disease
Enrollment 120 participants
Start Date 2026-03-09
Primary Completion 2028-09 (estimated)
Study Completion 2028-09 (estimated)
Updated on ClinicalTrials.gov 2026-07-10