UAB Alzheimer's Disease Center Core Cohort - Tau Imaging Substudy

Who is this study for? Patients enrolled in the UAB-ADC study
What treatments are being studied? [F-18]AV-1451-PET
Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

The primary objective of this study is to measure the concentration and the regional brain distribution of pathologic tau deposition using the PET tracer AV-1451 in participants in the UAB-ADC cohort. The amount and distribution of AV-1451 in the brain will be correlated to demographic, clinical, genetic, and biospecimen data acquired through the separate ongoing UAB-ADC study. Assessment of interactions between race and vascular risk factors, brain tau levels measured with AV-1451-PET, and cognitive status will be the primary outcome of this imaging study. Individuals participating in this AV-1451-PET/MRI study will also be enrolled in an ongoing \[C-11\]PiB-PET/MRI study (IRB-300001005, IND-138128), and their amyloid, tau and cognitive statuses will be compared in terms of race and vascular risk factors.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 50
Healthy Volunteers: t
View:

• Enrollment in the UAB-ADC study under a separate IRB-approved research protocol.

• Enrollment in the UAB-ADC amyloid-PET substudy under a separate IRB-approved research protocol. The amyloid-PET study does not have to have been completed prior to enrollment and participation in this tau-PET study.

• Negative urine or serum hCG test within 2 days of \[F-18\]AV-1451 administration in women of child bearing potential. Women who are post-menopausal with at least 1 year since last menses or documented surgical sterilization will not require pregnancy testing.

Locations
United States
Alabama
UAB
RECRUITING
Birmingham
Contact Information
Primary
Chinara Dosse
cdosse@uabmc.edu
(205) 934-4501
Backup
Carol Chambless
cchambless@uabmc.edu
(205) 975-9569
Time Frame
Start Date: 2020-07-08
Estimated Completion Date: 2026-07-08
Participants
Target number of participants: 160
Treatments
Experimental: [F-18]AV-1451-PET/MRI
All participants in this study will undergo a tau-PET imaging using the tracer \[F-18\]AV-1451 with a simultaneous PET/MRI system. The \[F-18\]AV-1451 dosage is 740MBq (10 mCi) given intravenously, and the PET/MRI imaging will occur 75-105 min after tracer injection.
Related Therapeutic Areas
Sponsors
Leads: University of Alabama at Birmingham
Collaborators: National Institute on Aging (NIA)

This content was sourced from clinicaltrials.gov

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