Imaging Inflammation in Alzheimer's Disease With 11C-ER176

Sponsor
William Charles Kreisl (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT03744312
Collaborator
(none)
50
1
2
46.3
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Study Details

Study Description

Brief Summary

This study is being done to learn about inflammation in the brain of those with Alzheimer's disease (AD). The purpose of this study is to determine if 11C-ER176 is able to accurately measure inflammation in patients with Alzheimer's disease. Both patients (with either mild cognitive impairment (MCI) or Alzheimer's disease) and healthy controls (participants without memory complaints or impairment) will be included in this study.

Condition or Disease Intervention/Treatment Phase
Phase 1/Phase 2

Detailed Description

Inflammation likely plays a role in the damage to the brain caused by Alzheimer's disease.

Accurately measuring inflammation in the brain could provide new information about the mechanisms that cause Alzheimer's disease, and could help identify new treatments that reduce inflammation. Positron emission tomography (PET) imaging is a type of brain scanning method that allows investigators to measure small molecules in the brain. ER176-PET was recently developed as an improved method for measuring brain inflammation. However, ER176-PET has not yet been used in patients with Alzheimer's disease. The investigators propose to use ER176-PET imaging in subjects with mild cognitive impairment (a very early stage of Alzheimer's disease) or mild Alzheimer's disease to compare the amount of inflammation with that seen in older control subjects. The investigators will first use a "gold standard" method of measuring ER176 in brain that requires sampling arterial blood during the scan. The investigators will compare these results to those obtained using novel methods that don't require blood sampling. The investigators hope to show that ER176 is a useful tool for measuring inflammation in Alzheimer's disease, and that the investigators can develop a way to obtain ER176 PET scans that don't require arterial blood sampling.

This study uses a special type of scan called a PET scan to take pictures of the brain. During the PET scan, a special dye is injected into the body. Two types of dye will be used in this study: Florbetaben and 11C-ER176. Florbetaben sticks to amyloid plaques, which are in the brain in Alzheimer's disease. Florbetaben has been approved by the Food and Drug Administration to help diagnose Alzheimer's disease. 11C-ER176 sticks to parts of the brain where there is inflammation. Past studies have shown that inflammation is present in the brains of patients with Alzheimer's disease.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Imaging Inflammation in Alzheimer's Disease With 11C-ER176
Actual Study Start Date :
Sep 10, 2018
Anticipated Primary Completion Date :
Jul 20, 2022
Anticipated Study Completion Date :
Jul 20, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Cognitive impairment

Alzheimer's disease (mild cognitive impairment or mild stage Alzheimer's disease dementia)

Drug: 11C-ER176
11C-ER176 sticks to parts of the brain where there is inflammation. Past studies have shown that inflammation is present in the brains of patients with Alzheimer's disease. The purpose of this study is to determine if 11C-ER176 is able to accurately measure inflammation in patients with Alzheimer's disease.
Other Names:
  • [11C] ER176
  • Drug: Florbetaben
    Florbetaben sticks to amyloid plaques, which are in the brain in Alzheimer's disease.
    Other Names:
  • NeuraCeq
  • Active Comparator: No cognitive impairment

    Healthy Controls

    Drug: 11C-ER176
    11C-ER176 sticks to parts of the brain where there is inflammation. Past studies have shown that inflammation is present in the brains of patients with Alzheimer's disease. The purpose of this study is to determine if 11C-ER176 is able to accurately measure inflammation in patients with Alzheimer's disease.
    Other Names:
  • [11C] ER176
  • Drug: Florbetaben
    Florbetaben sticks to amyloid plaques, which are in the brain in Alzheimer's disease.
    Other Names:
  • NeuraCeq
  • Outcome Measures

    Primary Outcome Measures

    1. 11C-ER176 total distribution volume [Up to one year from baseline]

      Total distribution volume reflects the amount of TSPO (the inflammatory protein that 11C-ER176 sticks to) in the brain. This measure requires arterial blood sampling.

    Secondary Outcome Measures

    1. 11C-ER176 Standardized Uptake Value Ratio [Up to one year from baseline]

      The standardize uptake value ratio is the concentration of radioactivity measured from the 11C-ER176 PET scan in the cortex compared to the uptake in the cerebellum (pseudo-reference region).

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    50 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    1. Age 50 and older

    2. Meet criteria for either a) amnestic mild cognitive impairment or Alzheimer's disease, or b) have no cognitive impairment

    3. If you are unable to provide informed consent, you must have a surrogate decision maker and be able to verbally assent to the study procedures

    4. Written and oral fluency in English

    5. Able to participate in all scheduled evaluations and to complete all required tests and procedures.

    6. In the opinion of the investigator, you must be considered likely to comply with the study protocol and to have a high probability of completing the study.

    Exclusion Criteria:
    1. Past or present history of certain brain disorders other than MCI or AD.

    2. Certain significant medical conditions, which make study procedures of the current study unsafe. Such serious medical conditions include uncontrolled epilepsy and multiple serious injuries.

    3. Contraindication to MRI scanning

    4. Conditions precluding entry into the scanners (e.g. morbid obesity, claustrophobia, etc.).

    5. Exposure to research related radiation in the past year that, when combined with this study, would place you above the allowable limits.

    6. Participation in the last year in a clinical trial for a disease modifying drug for AD.

    7. Inability to have a catheter in your vein for the injection of radioligand.

    8. Inability to have blood drawn from your veins.

    9. Taking anticoagulant medication (e.g., warfarin).

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Columbia University Medical Center New York New York United States 10032

    Sponsors and Collaborators

    • William Charles Kreisl

    Investigators

    • Principal Investigator: William C Kreisl, M.D., Columbia University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    William Charles Kreisl, Boris and Rose Katz Assistant Professor of Neurology, Columbia University
    ClinicalTrials.gov Identifier:
    NCT03744312
    Other Study ID Numbers:
    • AAAR6570
    First Posted:
    Nov 16, 2018
    Last Update Posted:
    Aug 5, 2021
    Last Verified:
    Aug 1, 2021
    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 William Charles Kreisl, Boris and Rose Katz Assistant Professor of Neurology, Columbia University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 5, 2021