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Clinical Trial Summary

The overall goal of this protocol is to evaluate the imaging characteristics of [18F]PI-2620 using positron emission tomography (PET) in patients with progressive supranuclear palsy, Richardson's syndrome (PSP-RS)


Clinical Trial Description

The imaging characteristics of [18F]PI-2620 using positron emission tomography (PET) in patients with progressive supranuclear palsy, Richardson's syndrome (PSP-RS) will be evaluated by a) determining the test-retest variability of the [18F]PI-2620 binding parameters in brain of patients with PSP-RS and non-demented controls (NDC). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05187546
Study type Interventional
Source Life Molecular Imaging SA
Contact Audrey Perrotin, PhD
Phone +49 (0)30 461 1246 03
Email [email protected]
Status Recruiting
Phase Phase 1
Start date January 2022
Completion date December 2022

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