GLP1R in Parkinson's Disease
- Sponsor
- Oslo University Hospital
- Study ID
- NCT03659682
- Phase
- PHASE2
- Status
- Unknown
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 40 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- Semaglutide — DRUGsubcutaneous, 1.0 mg, weekly, 48 months
Study Details
The purpose of the study is to test the neuroprotective and anti-inflammatory properties of semaglutide in idiopathic Parkinson's disease (PD)
Key Dates
- Start date
- Jan 2, 2019
- Status verified
- Sep 2018
- Primary completion
- Dec 31, 2024
- Completion
- Dec 31, 2024
Study Design
- Enrollment
- 120 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- CROSSOVER
- Primary purpose
- TREATMENT
Arms
- Active Comparator: semaglutideOzempic- 1.0 mg administered subcutaneously once weekly
- Placebo Comparator: placeboPlacebo, 1.0 mg administered subcutaneously once weekly
Primary Outcome Measure
Motor Function [ Time Frame: 48 months ]
Central Contacts
- Hanne F Harbo, MD, PhD+47 230 72246
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