This is a phase 3, open-label, multiple-center, non-randomized single dose study to assess the safety and efficacy of \[123I\]NAV5001 SPECT imaging in aiding in the differentiaion of parkinsonian syndromes from non-parkinsonian tremor.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
13
A single intravenous dose of 8.0 ± 1.0 mCi
Xenoscience, Inc.
Phoenix, Arizona, United States
Compass Research
Orlando, Florida, United States
The incidence of Parkinson' Syndrome based on the Movement Disorder Specialist Consensus Panel
Time frame: One Year
The incidence of positve [123I]NAV5001 SPECT brain scans
Time frame: One Year
The incidence of Parkinson' Syndrome based on the on-site neurologist assessment
Time frame: Baseline
The incidence of Parkinson' Syndrome based on the on-site neurologist assessment at 6 months
Time frame: 6 months
The incidence of Parkinson' Syndrome based on the on-site neurologist assessment at 1 year
Time frame: 1 Year
Incidence of adverse events post baseline
Time frame: 1 year
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