ClinicalTrials.gg
RecruitingNCT07000851I-CANUpdated Jul 14, 2026

Imaging Studies in Corticobasal Syndrome

An observational study in Cortico Basal Degeneration, Corticobasal Syndrome and Corticobasal Syndrome(CBS), sponsored by Jennifer Whitwell. Recruiting at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-07-14.

Sponsored by Jennifer Whitwell · Observational

From the registry’s dates

  • Started Jun 2025; still recruiting 1 year 4 months later.
Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
80
Ages
18 Years and older
Sex
All
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Study summary

The primary goal of this study is to investigate inflammation and white matter damage in corticobasal syndrome and determine whether these processes are related to each other. The investigator's will address our goal by using neuroimaging and blood plasma biomarkers, as well as molecular pathology.

Read the detailed description

Corticobasal syndrome (CBS) is a neurodegenerative disorder characterized by cognitive and behavioral change, as well as asymmetric parkinsonism, dystonia, myoclonus, and limb apraxia. Emerging evidence suggests neuroinflammation plays a key role in the pathogenesis of neurodegenerative disease, including the 4R tauopathies and AD, and neuroinflammation has been linked mechanistically to damage of the white matter. The primary goal of this study is to investigate inflammation and white matter damage using imaging and blood samples.

The investigator's will use the PET ligand 11C-ER176 to assess patterns of neuroinflammation in the brain and Neurite Orientation Dispersion and Density Imaging (NODDI) to measure white matter microstructure, including axonal density and alignment. The investigator's will also investigate blood plasma metrics, including neurofilament light chain and plasma glial fibrillary acidic protein (GFAP) that measure neuroaxonal injury and astrogliosis, and inflammation and tau metrics. The investigator's will employ beta-amyloid (A) and tau (T) PET to subdivide the CBS patients into those with biomarker AD (A+T+, CBS-AD) and those without biomarker AD (CBS-4R). The investigator's will also compare these groups to disease controls with typical amnestic biomarker AD (Amn-AD) and healthy controls (HC) that have previously been recruited for other grants (existing data collected under approved IRBs).

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Conditions studied

  • Cortico Basal Degeneration
  • Corticobasal Syndrome
  • Corticobasal Syndrome(CBS)
  • Corticobasal Degeneration
  • Corticobasal Degeneration (CBD)
  • Corticobasal Syndrome (CBS)

Keywords

  • neurodegeneration
  • neurodegenerative disease
  • cbs
  • cbd
  • corticobasal syndrome
  • corticobasal degeneration
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In context

Corticobasal Degeneration

64 studies on the registry are indexed under Corticobasal Degeneration; 26 are open to participants now.

This study's planned enrollment of 80 is below the median of 186 across 35 observational studies indexed under Corticobasal Degeneration.

Browse Corticobasal Degeneration studies →

Lead sponsor

This is the only study on the registry with Jennifer Whitwell as lead sponsor.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

All patients who meet criteria are eligible to participate

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age 18 years or older
  • Meet possible or probable CBS criteria

Exclusion criteria

Exclusion Criteria:

  • Subjects will be excluded if MRI is (due to implanted device, severe claustrophobia, etc)
  • Subjects will be excluded if they have a concurrent illnesses or structural abnormality that could account for the CBS syndrome
  • Subjects will be excluded if they have a mutation in the progranulin gene
  • Subjects will excluded if they have received anti-Aβ therapy
  • Women who are pregnant will be excluded
  • Subjects will be excluded if they are actively taking daily anti-inflammatory medications (NSAIDs, corticosteriods, etc)
  • Subjects will be excluded if they have generalized inflammatory condition and treatment with , corticoid/, steroidal or non-steroidal anti-inflammatory medication within 2 weeks of scanning
Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

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Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
80 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • Corticobasal Syndrome

    patients diagnosed with cbs

    Diagnostic Test: C-11 ER176 Radiotracer · Diagnostic Test: C-11 PiB · Diagnostic Test: AV1451 Tau

  • Healthy Control

    Healthy Control Volunteer

    Diagnostic Test: C-11 ER176 Radiotracer · Diagnostic Test: C-11 PiB · Diagnostic Test: AV1451 Tau

Interventions

  • Diagnostic testC-11 ER176 Radiotracer

    PET scan looking for inflammation

  • Diagnostic testC-11 PiB

    PET scan looking for amyloid protein

  • Diagnostic testAV1451 Tau

    Pet scan looking for Tau protein

06

What researchers measure

Primary outcomes

  1. The investigators will use C-11 ER176 PET imaging to evaluate neuroinflammation and white matter integrity in CBS

    Measure whether regional patterns of ER176-PET uptake and white matter microstructure abnormalities using NODDI differ between CBS-4R, CBS-AD, Amn-AD, and HC.

    Time frame: approximately 4-5 years into study visits

Secondary outcomes

  1. the investigators will use blood samples to assess inflammatory and tau blood plasma metrics in CBS.

    Measure whether plasma metrics differ between CBS-4R, CBS-AD, Amn-AD, and HC.

    Time frame: approximately 4-5 years into study visits

Other outcomes

  1. The investigators will use MR imaging to compare regional markers of inflammation, white matter integrity and tau burden in autopsy tissue from patients with CBS from two different 4R tauopathies and CBS-AD.

    Time frame: Approximately 8-10 years after study completion

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Study locations

1 of 1 sites recruiting
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 14, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07000851
Lead sponsor
Jennifer Whitwell
Responsible party
Jennifer Whitwell (Associate Consultant II, Mayo Clinic) — Sponsor-investigator
First posted
Jun 3, 2025
Start date
Jun 25, 2025
Primary completion
Mar 30, 2030 (estimated)
Completion
Mar 30, 2031 (estimated)
Last update
Jul 14, 2026

Study contacts

Megan J Meyer, M.B.A.
Contact
meyer.megan6@mayo.edu
507-293-1164
Sarah M Boland, CCRP
Contact
boland.sarah@mayo.edu
507284-3863
Jennifer Whitwell, Ph.D.
principal investigator · Mayo Clinic

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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