A scan that sees Alzheimer's tangles? trial puts tau tracer to the test
NCT ID NCT07752784
First seen Aug 07, 2026 · Last updated Aug 18, 2026 · Updated 4 times
Summary
This trial tests whether a single injection of [18F]-APN-1607, a radioactive tracer that binds to tau protein, can produce PET images that match the actual tau buildup found in the brain after death. It includes healthy volunteers and people with mild cognitive impairment or Alzheimer's dementia, all aged 50 or older. The goal is to see if this imaging method can reliably detect Alzheimer's-related brain changes, which could lead to better diagnosis without needing an autopsy.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- [18F]-APN-1607, a radioactive tracer for PET imaging that binds to tau protein in the brain
- What this could lead to
- If successful, this could validate a PET scan as a reliable way to detect Alzheimer's-related brain changes in living people, potentially improving diagnosis and monitoring.
- What could go wrong
- The trial is small (12 participants) and early, so results may not be conclusive. The tracer's accuracy could be limited, and it involves radiation exposure from the PET scan.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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About 12 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Aug 2027
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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50 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Able to understand and voluntarily sign a written informed consent form (ICF). 2. Age≥50 years, male or female. 3. Charlson Comorbidity Index (CCI)≥5. 4. Able to tolerate imaging procedures. 5. For MCI or AD subjects: clinically diagnosed as AD-derived cognitive impairment or Alzheimer's dementia. 6. For HV subjects: no known personal or family history of AD-derived dementia. Exclusion Criteria: 1. Confirmed brain structural abnormalities that may affect PET reading, e.g., large stroke (infarct area\>4 cm) or intracranial space-occupying lesion. 2. Currently having clinically significant infectious diseases: HIV, hepatitis, etc. 3. Currently participating in any investigational clinical trial. 4. Previous participation in clinical studies of amyloid or tau-targeting agents. 5. Suspected hepatic encephalopathy. 6. Allergy to the investigational drug or any of its components. 7. Currently pregnant or breastfeeding. 8. Currently having a disease or condition that prolongs the QT interval.
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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 places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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.
Contacts and locations
Locations
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Beijing Tiantan Hospital, Capital Medical University
RECRUITINGBeijing, Beijing Municipality, 100070, China
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