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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03283449
Other study ID # STU00200893
Secondary ID R01AG056258
Status Recruiting
Phase Phase 1
First received
Last updated
Start date February 2016
Est. completion date March 30, 2024

Study information

Verified date March 2024
Source Northwestern University
Contact Seyi Adeolu
Phone 312-503-2398
Email PPA.Research@northwestern.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Recruiting
Enrollment 70
Est. completion date March 30, 2024
Est. primary completion date March 30, 2024
Accepts healthy volunteers No
Gender All
Age group 20 Years to 100 Years
Eligibility Inclusion Criteria: - Must have primary progressive aphasia Exclusion Criteria: - Pregnancy - Breastfeeding - Receiving radiation clinically

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
18F-AV-1451

Device:
PET
PET scanner for brain imaging

Locations

Country Name City State
United States Cognitive Neurology and Alzheimer's Disease Center - Northwestern University Chicago Illinois

Sponsors (2)

Lead Sponsor Collaborator
Northwestern University National Institute on Aging (NIA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Tau levels in PPA participants Tau deposition as measured by 18F-AV-1451 standardized uptake value ratio (SUVR) in cortical and medial temporal regions. 2 years