New imaging study aims to spot immune cells in Alzheimer's brains
NCT ID NCT07611357
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study uses a special full-body PET scan to look for activated T cells (a type of immune cell) in the brain and body of people with Alzheimer's disease. Ten participants with Alzheimer's and some healthy volunteers will get the scan to compare results. The goal is to better understand how the immune system may be involved in Alzheimer's, not to test a treatment.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 10 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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May 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2029
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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55 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age ≥ 55 years 2. Prior volumetric brain MRI available. If the prior MRI scan is not acquired within 6 months of \[18F\]F-AraG imaging or if the investigator determines that prior MRI scan cannot be used, a new MRI scan will be acquired. 3. Able to tolerate a PET scan, and willingness and ability to comply with all protocol required procedures. 4. For participants of reproductive potential - defined as individuals who have not been post-menopausal for at least 24 consecutive months (i.e., who have had menses within the preceding 24 months), or who have not undergone surgical sterilization, specifically hysterectomy and/or bilateral oophorectomy or bilateral salpingectomy - willingness to use effective double barrier contraceptive methods (excluding withdrawal or timing methods) up to 1 day after the administration of \[18F\]F-AraG 5. Subjects with possible or probable AD based on the NIA-Alzheimer's Association working group's diagnostic guidelines for AD. 6. Have a study partner who has significant interaction with the subject and can report on the subject's activities of daily living. Exclusion Criteria: 1. Clinically significant psychiatric disease other than depression. 2. Structural brain abnormalities on MRI (e.g. large infarct or mass) likely to interfere with interpretation of a PET scan. 3. History of significant alcohol or substance abuse/dependence within the past 5 years. 4. Non-study related radiopharmaceutical imaging or treatment procedure within 7 days prior to the PET imaging session. 5. Current or recent investigational drug use, defined as receiving any investigational medications or participation in another investigational drug trial within the last 30 days. 6. Serious comorbidities (malignant and nonmalignant disease or other conditions) that in the opinion of the investigator could compromise study objectives. 7. Conditions affecting immune function or conditions caused by immune system malfunction that could interfere with imaging, including known inflammatory or immune disorders, systemic malignancy, or chronic viral infections. 8. Pregnant or nursing individuals. All participants of reproductive potential will undergo a urine or HCG serum pregnancy test with a sensitivity of at least 25 mIU/mL at screening and on the day of PET/CT imaging. 9. Prior allogeneic stem cell or solid organ transplant. 10. Previously diagnosed myelodysplasia syndrome or history of lymphoproliferative disease prior to study entry. 11. Active systemic autoimmune diseases. 12. Self-reported history of dysphoria or anxiety in closed spaces (i.e., uncontrolled claustrophobia). 13. Concurrent or prior enrollment in a separate research study involving a PET scan performed within the last 12 months for research purposes only. 14. Body weight is more than 240 kg (529 pounds) 15. Recent use of medications containing guanosine or cysteine analogs. 16. Any other criteria which would make the participant unsuitable for study participation, as determined by the Principal Investigator.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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Other studies related to the condition(s) this trial covers.
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