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Exploring the Utility of [18F]3F4AP for Demyelination Imaging

Exploring the Utility of [18F]3F4AP for Demyelination Imaging

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06999434
Enrollment
105
Registered
2025-05-31
Start date
2025-05-05
Completion date
2030-05-05
Last updated
2025-05-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Demyelinating Disorders, MCI, Alzheimer's Disease (AD), MS (Multiple Sclerosis), SCI - Spinal Cord Injury, Spinal Radiculopathy

Keywords

3F4AP, Demyelinating Disorders, MS, SCI, AD

Brief summary

The overall objective is to obtain an assessment of the pharmacokinetics of \[18F\]3F4AP in healthy volunteers and subjects with demyelinating diseases such as mild cognitive impairment (MCI), Alzheimer's Disease (AD), Multiple Sclerosis (MS), Spinal Cord Injury (SCI) and Spinal radiculopathy (SR).

Interventions

DRUG[ 18F]3F4AP

PET Scan #3

DRUG[18F]MK6240

PET Scan #2

PET Scan #1

Sponsors

National Institute for Biomedical Imaging and Bioengineering (NIBIB)
CollaboratorNIH
National Institute on Aging (NIA)
CollaboratorNIH
Yale University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

Inclusion: 1. Male and Female subjects must be ≥18 and \<90 years of age; 2. Able to understand and provide informed consent prior to study procedures 3. Must be in good health Exclusion: 1. Less than 18 years of age; 2. Pregnant or breastfeeding; 3. Any significant systemic illness or unstable medical condition; 4. Pre-existing medical conditions or claustrophobic reactions; 5. Research-related radiation exposure exceeds current PET Center guidelines (i.e. 50 mSv in the prior 12 months); 6. History of a bleeding disorder or are currently taking anticoagulants.

Design outcomes

Primary

MeasureTime frameDescription
Associations between imaging modalities and biomarkers.5 yearsThe Pearson correlation coefficient r will be used to assess the strength of the linear correlations between outcome measures. A P value of 0.05 or less will be considered statistically significant.
Demyelination5 years\[18F\]3F4AP will be used to measure demyelination. On the MR images, after co-registration and alignment, signal from pre- and post-contrast T1-weighted images, T2-weighted image, ratio between T1- and T2-weighted images (T1/T2) will be calculated to assess demyelination and white matter lesion (WML) on MR sequences.
Tau burden5 years\[18F\]MK6240 will be used to measure Tau burden.
Amyloid burden5 years\[11C\]PiB will reflect amyloid burden.
Tracer rate constant5 yearsThe tracer rate constant for transfer from arterial plasma to tissue K1 and relative delivery R1 will also be estimated using tracer kineticmodeling technique, to provide measures of cerebral perfusion or CBF.
Tracers volume of distribution (VT)5 yearsPET images measured with \[ 18F\]3F4AP will quantify demyelination, those obtained with \[18F\]MK6240 will quantify tau burden and those obtained with \[11C\]PiB will reflect amyloid burden. PET images acquired with \[18F\]3F4AP, \[18F\]MK6240 and \[11C\]PiB, will measure the tracers volume of distribution (VT).
Distribution volume ratio (DVR)5 yearsPET images acquired with \[18F\]3F4AP, \[18F\]MK6240 and \[11C\]PiB, will measure the tracers distribution volume ratio (DVR).
Binding potential (BPND)5 yearsPET images acquired with \[18F\]3F4AP, \[18F\]MK6240 and \[11C\]PiB, will measure the tracers binding potential (BPND).

Secondary

MeasureTime frameDescription
Measure of cerebrovascular burden5 yearsvolume of White matter hyperintensities (WMH) on T1 images or T2 images
Measure of White matter lesions (WML)5 yearsThe total WML load score will be calculated as the sum of the frequency of lesions multiplied by their volume.
MR/MRSI images5 yearsEvaluated to determine the effect of pulse sequence parameters and/or hardware configuration on image quality. The images acquired with different pulse sequence parameters or MR hardware configurations will be compared. Comparison of the MR images entails comparing the result of specific image quality measures such as signal-to-noise ratio (SNR) and contrast-to-noise ratio (CNR) as well as the level of image artifacts
Measure of brain atrophy5 yearsT1 images segmented and parcellated using FreeSurfer will be used to calculate cortical volumes, including the total cortical volume but also the hippocampal volume and will serve as proxies for neocortical and allocortical atrophy.

Countries

United States

Contacts

Primary ContactShannan Henry
shannan.henry@yale.edu+1 (203) 737-5278
Backup ContactKayla Cottiers
kayla.cottiers@yale.edu203-737-7496

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026