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Evaluating the effect of inhaled levodopa (Inbrija®) for early morning off in Parkinson’s disease

Status
Not yet recruiting
Phases
Phase 3
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2026-526465-18-00
Enrollment
22
Registered
2026-06-25
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

parkinson's disease

Brief summary

Time in minutes from completion of the assigned morning study dose (T0) to the first PKG-defined ON state per valid morning, evaluated within a 0–120-minute post-dose window and truncated at 120 minutes.

Detailed description

Patient-reported time-to-ON following the morning dose, Overall preferred morning treatment, Experience with use of the treatment, Early-morning motor function, ease of initiating morning activities, perceived independence, and perceived confidence/security, Unified Parkinson’s Disease Rating Scale, Part II (MDS-UPDRS-II), Parkinson’s Disease Questionnaire (PDQ-8), Non-Motor Symptoms Scale (MDS-NMS-Q), Proportion of PKG epochs below a fixed bradykinesia threshold (BKS < 25) within predefined post-dose windows (0–10, 0–20, 0–30, and 0–60 minutes after morning dosing), Proportion of PKG epochs below the individualized threshold (BKS < θ) within the same post-dose windows, Early-morning physical activity and inactivity, quantified using PKG-derived activity metrics (including immobility time), Pre-dose baseline motor severity during run-in, defined as the mean PKG BKS in the 10 minutes preceding the participant’s first levodopa/DDCI dose of the day., Time spent in OFF, ON, and dyskinetic states over the day, expressed as the proportion of valid daytime epochs in each state. States will be defined using fixed PKG thresholds: OFF: BKS ≥ 25 ON: BKS < 25 and DKS ≤ 9 Dyskinesia: DKS > 9, Sleep-related PKG metrics derived from nocturnal recordings (e.g., total sleep duration, sleep efficiency, nocturnal immobility, and sleep fragmentation), summarised per night and averaged within each intervention period.

Interventions

DRUGInbrija 33 mg inhalation powder
DRUGMadopar Quick "125"

Sponsors

Region Hovedstaden
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Time in minutes from completion of the assigned morning study dose (T0) to the first PKG-defined ON state per valid morning, evaluated within a 0–120-minute post-dose window and truncated at 120 minutes.

Secondary

MeasureTime frame
Patient-reported time-to-ON following the morning dose, Overall preferred morning treatment, Experience with use of the treatment, Early-morning motor function, ease of initiating morning activities, perceived independence, and perceived confidence/security, Unified Parkinson’s Disease Rating Scale, Part II (MDS-UPDRS-II), Parkinson’s Disease Questionnaire (PDQ-8), Non-Motor Symptoms Scale (MDS-NMS-Q), Proportion of PKG epochs below a fixed bradykinesia threshold (BKS < 25) within predefined post-dose windows (0–10, 0–20, 0–30, and 0–60 minutes after morning dosing), Proportion of PKG epochs below the individualized threshold (BKS < θ) within the same post-dose windows, Early-morning physical activity and inactivity, quantified using PKG-derived activity metrics (including immobility time), Pre-dose baseline motor severity during run-in, defined as the mean PKG BKS in the 10 minutes preceding the participant’s first levodopa/DDCI dose of the day., Time spent in OFF, ON, and dyskinetic

Outcome results

None listed

Source: EU CTIS · Data processed: Jun 26, 2026