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Clinical Trials/NCT03283449
NCT03283449
Completed
Phase 1

Tau PET Imaging in Atypical Dementias

University of Chicago1 site in 1 country70 target enrollmentFebruary 2016

Overview

Phase
Phase 1
Intervention
18F-AV-1451
Conditions
Primary Progressive Aphasia With Suspected Alzheimer's Disease
Sponsor
University of Chicago
Enrollment
70
Locations
1
Primary Endpoint
Tau levels in PPA participants
Status
Completed
Last Updated
last year

Overview

Brief Summary

The goal of this study is to demonstrate the feasibility of mapping tau pathology in subjects with Primary Progressive Aphasia, using PET protocol with F-AV-1451 (trade name AV-1451) and to systematically document the extent and location of tau pathology in PPA patients in vivo using the same techniques.

Registry
clinicaltrials.gov
Start Date
February 2016
End Date
February 28, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Must have primary progressive aphasia

Exclusion Criteria

  • Pregnancy
  • Breastfeeding
  • Receiving radiation clinically

Arms & Interventions

AV-1451 Recipients

Participants in this arm of the study will all receive an injection of 10 Mci of AV-1451 and then be scanned in a PET scanner for brain imaging.

Intervention: 18F-AV-1451

AV-1451 Recipients

Participants in this arm of the study will all receive an injection of 10 Mci of AV-1451 and then be scanned in a PET scanner for brain imaging.

Intervention: PET

Outcomes

Primary Outcomes

Tau levels in PPA participants

Time Frame: 2 years

Tau deposition as measured by 18F-AV-1451 standardized uptake value ratio (SUVR) in cortical and medial temporal regions.

Study Sites (1)

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