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Test-retest Study With [18F]PI-2620 in PSP-RS and NDC

Progressive Supranuclear Palsy Clinical Trial

Official title:
An Open Label, Single Center Study to Evaluate the Safety and Test-retest Characteristics of [18F]PI-2620 as PET Radioligand for Imaging Tau Deposition in the Brains of Patients With Progressive Supranuclear Palsy Richardson Syndrome (PSP-RS) Compared to Non-demented Controls (NDC)

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

Clinical Trial Details
NCT number NCT05187546
Study type Interventional
Source Life Molecular Imaging SA
Contact
Status Completed
Phase Phase 1
Start date March 10, 2022
Completion date March 5, 2024
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