Actively Recruiting

Age: 18Years +
All Genders
NCT06937034

Study on Practical ExperienceS of Treatment With Foslevodopa/foScaRbidopa in Advanced Parkinson's Disease

Led by AbbVie · Updated on 2025-08-05

2000

Participants Needed

4

Research Sites

33 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Main objective of this study is to describe the evolution of infusion settings (base, high and low infusion rates) of foslevodopa/foscarbidopa subcutaneous infusion (LDp/CDp) at different timepoints in the treatment of advanced Parkinson's disease (aPD) as captured in ONE-CRM.

CONDITIONS

Official Title

Study on Practical ExperienceS of Treatment With Foslevodopa/foScaRbidopa in Advanced Parkinson's Disease

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with levodopa-responsive idiopathic Parkinson's Disease
  • Prescribed foslevodopa/foscarbidopa continuous subcutaneous infusion (LDp/CDp CSCI) in routine clinical practice
  • Consented to be enrolled in the AbbVie Patient Support Program
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 4 locations

1

Medizinische Universitaet Graz /ID# 278569

Graz, Styria, Austria, 8010

Not Yet Recruiting

2

Medisch Spectrum Twente /ID# 276695

Enschede, Overijssel, Netherlands, 7512 KZ

Actively Recruiting

3

Universitatea De Medicină Și Farmacie Victor Babeș /ID# 276720

Timișoara, Timiș County, Romania, 300041

Actively Recruiting

4

Karolinska University Hospital Solna /ID# 277116

Solna, Stockholm County, Sweden, 171 64

Actively Recruiting

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Research Team

A

ABBVIE CALL CENTER

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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