Protocol Z: Imaging of Brain Structural/Functional Connectivity and Amyloid and Tau Lesions in APOE4 Carriers.

Sponsor
Tammie L. S. Benzinger, MD, PhD (Other)
Overall Status
Recruiting
CT.gov ID
NCT03816228
Collaborator
(none)
80
1
33
2.4

Study Details

Study Description

Brief Summary

This is a multi-center study at Washington University (WASH U), University of Southern California (USC), and Huntington Medical Research Institute (HMRI).The overall goal of both the AA program and the PPG program is to advance current knowledge on the vascular contributions to dementia particularly in individuals with the major genetic risk factor for late-onset AD, i.e., apolipoprotein E-ε4 (APOE4) gene that develop early vascular dysfunction and significant cerebrovascular pathology compared to non-carriers, and establish whether the neurovasculature plays a key role in cognitive decline, and therefore is a key new therapeutic target to treat dementia in APOE4 carriers.

Condition or Disease Intervention/Treatment Phase
  • Drug: F 18 T807 Flortaucipir

Study Design

Study Type:
Observational
Anticipated Enrollment :
80 participants
Observational Model:
Other
Time Perspective:
Prospective
Official Title:
Imaging of Brain Structural/Functional Connectivity and Amyloid and Tau Lesions in APOE4 Carriers. (IND 123119, Protocol Z)
Anticipated Study Start Date :
Sep 1, 2022
Anticipated Primary Completion Date :
Jan 1, 2025
Anticipated Study Completion Date :
Jun 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental Flortaucipir

Drug: F 18 T807 Flortaucipir
Participants will receive a single intravenous bolus injection of approximately 6.5-10mCi (240-370MBq) of F 18 T807. For those who cannot tolerate the full exam, participants will receive single intravenous bolus injection of approximately 6.5-10mCi (240-370MBq) of F 18 T807.
Other Names:
  • 18F-AV-1451
  • Outcome Measures

    Primary Outcome Measures

    1. F 18 T807 Standard Uptake Value Ratios [5 years]

      F 18 T807 Standard Uptake Value Ratios (SUVR) will be correlated with other imaging modalities (MRI, PET amyloid imaging) and cognitive performance.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Male or female, any race

    • Age > 18 years

    • Participation in one of the ongoing projects affiliated with the Knight ADRC at Washington University and referred by the MAP staff and a Washington University physician.

    • Normal cognition or early-stage symptomatic AD

    • Females of childbearing potential without documented history of menopause or hysterectomy who do participate must not be pregnant or breastfeeding at screening

    • (negative urine β-HCG within 24 hours prior to injection), and must agree to avoid becoming pregnant. Females of childbearing potential who do not agree to use reliable contraception or refrain from sexual activity for 24 hours following administration of flortaucipir injection.

    • Enrollment in DCE-MRI study

    • Capacity to give informed consent and follow study procedures

    Exclusion Criteria:
    • Any illness preventing cooperation with testing or longitudinal participation

    • Exclusion from the Knight ADRC or DIAN referring project

    • Has a high risk for Torsades de Pointes or is taking medications known to prolong or may prolong QT interval (refer to study attachment "Restricted Medication List").

    • MRI contraindications (e.g. electronic medical devices, severe claustrophobia, inability to lie still for long periods) that make it unsafe to participate in an MRI scan, using standard screening processes implemented by Washington University and Barnes-Jewish Hospital

    • Currently pregnant or breastfeeding

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Washington University School of Medicine Saint Louis Missouri United States 63110

    Sponsors and Collaborators

    • Tammie L. S. Benzinger, MD, PhD

    Investigators

    • Principal Investigator: Tammie Benzinger, MD, PhD, Washington University School of Medicine

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Tammie L. S. Benzinger, MD, PhD, Professor of Radiology & Neurological Surgery, Washington University School of Medicine
    ClinicalTrials.gov Identifier:
    NCT03816228
    Other Study ID Numbers:
    • IND 123119 Protocol Z
    First Posted:
    Jan 25, 2019
    Last Update Posted:
    Apr 15, 2022
    Last Verified:
    Apr 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Tammie L. S. Benzinger, MD, PhD, Professor of Radiology & Neurological Surgery, Washington University School of Medicine
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 15, 2022