Establishing 18F-PBR06 PET Imaging as a Viable Pharmacodynamic Endpoint in MSA
Completed · Phase 1/Phase 2
Conditions studied: MSA
In brief
The specific aims of the study are: Primary: To determine the presence and regional distribution of microglial activation, as assessed by \[F-18\]PBR06 PET, in subjects with MSA as compared to healthy controls, at baseline and at 9 months follow-up. Secondary: To assess the relationship between microglial activation and clinical progression at baseline and follow-up. Hypothesis: The working hypothesis is that there is microglial activation in Multiple System Atrophy and that the presence and regional distribution of microglial activation is different in MSA versus healthy controls and correlates with disease severity and comorbidities.
Key facts
- Study ID
- NCT03033680
- Run by
- Brigham and Women's Hospital
- People needed
- 17
- Starts
- 2017-03-24
- Expected to finish
- 2021-01-15
- Last updated by the study team
- 2021-04-26
Who can join
Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Probable MSA clinical diagnosis.
- Male and female subjects age 18 to 70 years.
- Motor symptom onset <2 years prior.
- Available brain MRI.
You may not qualify if…
- Individuals with a known alternate neurologic disorder, previous head injury, or substance abuse.
- Individuals with bipolar disease and schizophrenia
- Concurrent medical conditions that contraindicate study procedures.
- Women who are pregnant or nursing. Also, any woman who is seeking to become pregnant or suspects she is pregnant will be excluded from enrollment.
- Claustrophobia
- Corticosteroid treatment in the past four weeks
- Non-MRI compatible implanted devices
- Low Affinity binders
Where it is running
- Movement Disorders Clinic, 60 Fenwood Road — Boston, Massachusetts, United States
Full record on ClinicalTrials.gov
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