Study to Assess Real Life Effectiveness of Foslevodopa/Foscarbidopa in Adult German Participants at Initial Stages of Advanced Parkinson's Disease (EARLY-FOS)
Recruiting · NCT06916507 · Observational (researchers observe without assigning treatment) · Lead sponsor: AbbVie
View the official record on ClinicalTrials.gov →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 foscarbidopa/ foslevodopa is in treating German adult participants at initial stages of advanced Parkinson's disease under routine clinical practice. Foslevodopa/Foscarbidopa is an approved drug for the treatment of Parkinson's Disease. Approximately 125 adult participants who are prescribed Foslevodopa/Foscarbidopa by their doctors will be enrolled across approximately 20 sites in Germany. Participants will receive Foslevodopa/Foscarbidopa subcutaneous infusion as prescribed by their physician. Participants will be followed for up to 12 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.
Who can take part
Inclusion criteria
- Participants with a diagnosis of levodopa-responsive idiopathic Parkinson's disease
- Eligibility for foscarbidopa/foslevodopa (LDp/CDp) therapy in accordance with the approved local label
- Participant must be an adult male or female, 18-64 years of age
- Time since beginning of motor fluctuations ≤ 3 years
- The Hoehn and Yahr (H\&Y) stage \< 3 in the on-medication condition
- Decision to treat with LDp/CDp made by the clinician prior to any decision to approach the participant to participate in this study
Exclusion criteria
- Previous Exposure to any device-aided therapy (DAT).
- Any condition included in the contraindications section of the approved local LDp/CDp label.
- Participants with Mini mental state examination (MMSE) score \< 24
Where it is running
19 locations listed.
- Klinikum Bremen-Nord /ID# 275822 - Bremen, Germany
- Kliniken Schmieder - Allensbach /ID# 285402 - Allensbach, Baden-Wurttemberg, Germany
- Universitaetsklinikum Heidelberg /ID# 274164 - Heidelberg, Baden-Wurttemberg, Germany
- Universitaetsklinikum Tuebingen /ID# 275828 - Tübingen, Baden-Wurttemberg, Germany
- Praxis Prof. Kassubek/Prof. Riecker /ID# 274165 - Ulm, Baden-Wurttemberg, Germany
- Parkinson-Klinik Ortenau GmbH&Co KG /ID# 274161 - Wolfach, Baden-Wurttemberg, Germany
- Universitaetsklinikum Erlangen /ID# 280831 - Erlangen, Bavaria, Germany
- Klinikum Ingolstadt /ID# 280573 - Ingolstadt, Bavaria, Germany
- Klinikum der Universitaet Muenchen Grosshadern /ID# 274168 - Munich, Bavaria, Germany
- Klinikum Ernst von Bergmann /ID# 274176 - Potsdam, Brandenburg, Germany
- Universitaetskliniken Giessen und Marburg /ID# 274224 - Marburg, Hesse, Germany
- Knappschaftskrankenhaus Bottrop /ID# 274284 - Bottrop, North Rhine-Westphalia, Germany
- Cellitinnen-NTC Neurologisches Therapiecentrum /ID# 277865 - Cologne, North Rhine-Westphalia, Germany
- Klinikum Lippe Detmold /ID# 279451 - Detmold, North Rhine-Westphalia, Germany
- Klinikum Dortmund Klinikzentrum Mitte /ID# 280222 - Dortmund, North Rhine-Westphalia, Germany
- Universitaetsklinikum Carl Gustav Carus Dresden /ID# 274167 - Dresden, Saxony, Germany
- Krankenhaus Martha-Maria Halle-Dolau /ID# 274174 - Halle, Saxony-Anhalt, Germany
- Praxis MD Oehlwein /ID# 274222 - Gera, Thuringia, Germany
- Asklepios Fachklinikum Stadtroda /ID# 274162 - Stadtroda, Thuringia, Germany