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

Recruiting now

Conditions studied: Parkinson's Disease

In brief

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.

Key facts

Study ID

NCT07382440

Run by

AbbVie

People needed

120

Starts

2026-03-09

Expected to finish

2028-09-01

Last updated by the study team

2026-07-10

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Participant diagnosed with Advanced Parkinson's Disease (PD), aged 18 years or older able to provide voluntary informed consent.
• Participant evaluated for commercially available continuous subcutaneous Foslevodopa/Foscarbidopa (LDp/CDp) in the hospital at the clinician's discretion as part of his/her routine clinical care and the intention to administer subcutaneous LDp/CDp made prior to and independent of recruitment into the study.

You may not qualify if…

• Participant participating in an interventional research study (not including noninterventional studies) during the administration of LDp/CDp.
• Participant evaluated for commercially available continuous subcutaneous LD/CDp outside of the hospital.

Where it is running

• Imelda Ziekenhuis /ID# 279436 — Bonheiden, Antwerpen, Belgium (enrolling)
• Universitair Ziekenhuis Antwerpen /ID# 279434 — Edegem, Antwerpen, Belgium (enrolling)
• Chu Tivoli /ID# 279455 — La Louvière, Hainaut, Belgium (enrolling)
• Centre Hospitalier De Wallonie Picarde - Site Notre Dame /ID# 279452 — Tournai, Hainaut, Belgium (enrolling)
• Jessa Ziekenhuis - Campus Virga Jesse /ID# 279454 — Hasselt, Limburg, Belgium (enrolling)
• AZ Sint-Lucas /ID# 279453 — Ghent, Oost-Vlaanderen, Belgium (enrolling)
• UZ Gent /ID# 279433 — Ghent, Oost-Vlaanderen, Belgium (enrolling)
• Universitair Ziekenhuis Leuven /ID# 279439 — Leuven, Vlaams-Brabant, Belgium (enrolling)
• Algemeen Ziekenhuis Sint-Jan Brugge /ID# 279422 — Bruges, West-Vlaanderen, Belgium (enrolling)
• Az Groeninge Campus Kennedylaan /ID# 279423 — Kortrijk, West-Vlaanderen, Belgium (enrolling)
• AZ Oostende /ID# 279461 — Ostend, West-Vlaanderen, Belgium (enrolling)
• AZ-Delta. /ID# 279437 — Roeselare, West-Vlaanderen, Belgium (enrolling)

Full record on ClinicalTrials.gov

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