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

  • STATUS
    Recruiting
  • End date
    Dec 26, 2022
  • participants needed
    15
  • sponsor
    Life Molecular Imaging GmbH
Updated on 26 April 2022
Accepts healthy volunteers

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)

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).

Details
Condition Progressive Supranuclear Palsy
Treatment [18F]-PI2620
Clinical Study IdentifierNCT05187546
SponsorLife Molecular Imaging GmbH
Last Modified on26 April 2022

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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