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Effect of Exenatide on disease progression in early Parkinson’s disease.

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-520069-30-00
Acronym
Exenatide
Enrollment
60
Registered
2024-12-20
Start date
2020-01-21
Completion date
Unknown
Last updated
2024-12-20

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

FDG-PET network analysis at baseline, 9 and 21 months

Detailed description

MDS-UPDRS part 3 in OFF-medication state and accelerometer-based parameters of physical activity, MDS-UPDRS part 3 in ON-medication state, MDS-UPDRS parts 1, 2 and 4, biofluid-based parameters at baseline, 9, 18 and 21 months, LEDD at baseline, 3, 6, 9, 12, 15, 18 and 21 months, PDQ-39, NMSQuest, ESS at baseline, 6, 12, 18 months, MoCA at baseline, 9 and 21 months, B-SIT at baseline, 9 and 18 months, MADRS at screening, 6, 12 and 18 months

Interventions

DRUGBydureon 2 mg powder and solvent for prolonged-release suspension for injection
DRUGPowder and solvent for prolongedrelease suspension for injection in pre-filled pen

Sponsors

Region Stockholm – SLSO
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
FDG-PET network analysis at baseline, 9 and 21 months

Secondary

MeasureTime frame
MDS-UPDRS part 3 in OFF-medication state and accelerometer-based parameters of physical activity, MDS-UPDRS part 3 in ON-medication state, MDS-UPDRS parts 1, 2 and 4, biofluid-based parameters at baseline, 9, 18 and 21 months, LEDD at baseline, 3, 6, 9, 12, 15, 18 and 21 months, PDQ-39, NMSQuest, ESS at baseline, 6, 12, 18 months, MoCA at baseline, 9 and 21 months, B-SIT at baseline, 9 and 18 months, MADRS at screening, 6, 12 and 18 months

Countries

Sweden

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026