Actively Recruiting

Age: 18Years +
All Genders
NCT07382440

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

Led by AbbVie · Updated on 2026-04-07

120

Participants Needed

10

Research Sites

129 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with advanced Parkinson's Disease
  • Aged 18 years or older
  • Able to provide voluntary informed consent
  • Evaluated for continuous subcutaneous Foslevodopa/Foscarbidopa at hospital as part of routine care
  • Intention to start subcutaneous Foslevodopa/Foscarbidopa treatment made prior to study recruitment
Not Eligible

You will not qualify if you...

  • Currently participating in an interventional research study (excluding noninterventional studies) during treatment
  • Evaluated for continuous subcutaneous Foslevodopa/Foscarbidopa treatment outside of hospital

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 10 locations

1

Universitair Ziekenhuis Antwerpen /ID# 279434

Edegem, Antwerpen, Belgium, 2650

Actively Recruiting

2

Chu Tivoli /ID# 279455

La Louvière, Hainaut, Belgium, 7100

Actively Recruiting

3

Centre Hospitalier De Wallonie Picarde - Site Notre Dame /ID# 279452

Tournai, Hainaut, Belgium, 7500

Actively Recruiting

4

Jessa Ziekenhuis - Campus Virga Jesse /ID# 279454

Hasselt, Limburg, Belgium, 3500

Actively Recruiting

5

UZ Gent /ID# 279433

Ghent, Oost-Vlaanderen, Belgium, 9000

Actively Recruiting

6

Universitair Ziekenhuis Leuven /ID# 279439

Leuven, Vlaams-Brabant, Belgium, 3000

Actively Recruiting

7

AZ Sint-Jan Brugge /ID# 279422

Bruges, West-Vlaanderen, Belgium, 8000

Actively Recruiting

8

Az Groeninge Campus Kennedylaan /ID# 279423

Kortrijk, West-Vlaanderen, Belgium, 8500

Actively Recruiting

9

AZ Oostende /ID# 279461

Ostend, West-Vlaanderen, Belgium, 8400

Actively Recruiting

10

AZ-Delta. /ID# 279437

Roeselare, West-Vlaanderen, Belgium, 8800

Actively Recruiting

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Research Team

C

Clementine Semanaz

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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