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NCT07227896 · ClinicalTrials.gov registry record

Real-World Study of Foslevodopa/Foscarbidopa to Assess Quality of Life Outcomes in Adult Participants Earlier Within Advanced Parkinson Disease

A clinical trial, sponsored by AbbVie.

Not yet
Registry status
100
Enrollment target

NCT07227896: Clinical Trial study, sponsored by AbbVie.

NCT07227896 is a clinical trial that has not yet begun recruiting, run by AbbVie. The registered enrollment target is 100 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07227896 has not yet begun recruiting, sponsored by AbbVie.

NOT YET RECRUITING
Registry status
100 participants
Enrollment target

Study 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 earlier within advanced Parkinson disease under routine clinical practice. Foslevodopa/Foscarbidopa is an approved drug for the treatment of Parkinson's Disease. Approximately 100 adult participants who are prescribed Foslevodopa/Foscarbidopa by their doctors will be enrolled across approximately 40 sites across the world. Participants will receive Foslevodopa/Foscarbidopa subcutaneous infusion as prescribed by their physician. Participants will be followed for up to 6 months. There are no additional examinations due to the study but the participants and caregivers will need to fill several questionnaires to generate data on their motor function and well-being

Primary Outcome

The Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS) is an investigator-used rating tool to follow the longitudinal course of Parkinson's Disease (PD)

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2026-03-01
Est. Completion 2027-10
AbbVie

526 total trials

What is known before NCT07227896 opens enrollment

NCT07227896 is an observational study that tracks outcomes without assigning an intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap.

The record links to 0 conditions, and to 0 interventions.

NCT07227896 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07227896 about?

NCT07227896 is a clinical study titled "Real-World Study of Foslevodopa/Foscarbidopa to Assess Quality of Life Outcomes in Adult Participants Earlier Within Advanced Parkinson Disease". 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/Foscarbidop...

What is the current status of trial NCT07227896?

This trial is currently not yet recruiting. The enrollment target is 100 participants. The study started on 2026-03-01. Estimated completion is 2027-10.

Who is sponsoring clinical trial NCT07227896?

This trial is sponsored by AbbVie, which has 526 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT07227896, the US trial registry maintained by the National Library of Medicine. NCT07227896 (mid enrollment · none site footprint · not yet recruiting) retrieved and formatted by PlainTrial, see methodology.