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Radiolabeled TSPO Targeted Molecular Probe in Alzheimer's Disease.

Clinical Application of a Novel Radiolabeled Translocator Protein (TSPO) Targeted Small Molecular Probe in Neuroinflammation Imaging of Alzheimer's Disease.

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07105956
Enrollment
8
Registered
2025-08-06
Start date
2025-09-01
Completion date
2026-08-31
Last updated
2025-08-06

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

Conditions

Alzheimer's Disease (AD)

Brief summary

Evaluate the clinical application value of the novel radiolabeled TSPO-targeted molecular probe Gallium \[68Ga\]-DOTA-HK-011 in neuroinflammation imaging of Alzheimer's disease.

Interventions

None listed

Sponsors

Nanjing First Hospital, Nanjing Medical University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Volunteer for the trial, with the patient or their legal guardian signing the informed consent form. * Volunteers are not limited by gender, and the age range is from 18 to 75 years old, including both ends. * The patient is diagnosed with Alzheimer's disease (AD), supported by a positive amyloid PET scan. * The patient has completed Tau PET scan.

Exclusion criteria

* Individuals with a history of allergy to drugs chemically or biologically similar to TSPO, a history of atopy, or currently suffering from allergic diseases. * Use of anti-inflammatory drugs, including corticosteroids and immunosuppressants, within the past 14 days, which may interfere with the accuracy of inflammation imaging. * Presence of other coexisting neurological diseases, such as stroke, Parkinson's disease, brain tumors, or mental disorders, including depressive disorder and schizophrenia. * Severe cardiac, pulmonary, hepatic, or renal dysfunction, or uncontrolled systemic diseases; 5. Presence of metal implants contraindicated for MRI, including but not limited to cardiac pacemakers, artificial heart valves, and metal stents. * Claustrophobia or inability to tolerate prolonged examinations. * Pregnant women (defined as those with a positive urine pregnancy test) or breastfeeding women. * Patients whose physical condition is unsuitable for radioactive tracer-based imaging examinations. * Other circumstances deemed unsuitable for participation in the trial by the researcher.

Design outcomes

Primary

MeasureTime frame
SUVmax of lesion uptake value60min after administration

Countries

China

Contacts

Primary ContactFeng Wang
fengwangcn@hotmail.com+8602552271491

Outcome results

None listed

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