Skip to content

Tau PET Imaging With 18F-T807(AV1451) in Neurodegenerative Disorders

Tau PET Imaging With 18F-T807(AV1451) in Neurodegenerative Disorders

Status
UNKNOWN
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04926259
Enrollment
50
Registered
2021-06-15
Start date
2021-11-01
Completion date
2024-12-01
Last updated
2021-11-26

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

Conditions

Neurodegenerative Disorders

Brief summary

Alzheimer's disease, Parkinson's disease, and Huntington's disease are common neurodegenerative diseases. Tau is a microtubule-associated protein, and aggregated tau resulting from hyperphosphorylation is a pathological feature of a group of neurodegenerative diseases known as tauopathies. The 18F-T807 (AV1451) molecular probe is a novel molecularly targeted imaging agent that exhibits high affinity and good selectivity for tau.

Detailed description

In this study, 18F-T807 (AV1451) molecular probe PET/CT was used to monitor the regional distribution and the degree of deposition in patients with neurodegenerative diseases, and compared with clinical symptoms to evaluate its value in the early differential diagnosis of neurodegenerative diseases.

Interventions

DRUG18F-T807

Intravenous injection of one dose of 10mCi (370MBq, ±5%) 18F-T807. Each subject receive a single intravenous injection of 18F-T807, and undergo PET/CT imaging within the specificed time.

Sponsors

First Affiliated Hospital of Fujian Medical University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Patients or their families complain of significant memory impairment; * Objective memory impairment (e.g., tests of article identification, recall, delayed memory); * Be able to obtain complete diagnosis and treatment records and be able to carry out long-term follow-up; * Signed written consent.

Exclusion criteria

* Psychiatric disorders: including anxiety disorder, affective disorder, severe psychosis, or drug-induced psychosis; * Pregnancy or lactation.

Design outcomes

Primary

MeasureTime frameDescription
standardized uptake value ratio (SUVR)From right after tracer injection to 2-hours post-injectionthe ratio of radioactivity in a cerebral region to that in the cerebellum as a reference
Aβ42 in CSFWithin 2 hours prior to tracer injectionAβ42 (amyloid beta isoform 42) is significantly lower in the cerebrospinal fluid of patients with neurodegenerative diseases and is one of the biomarkers used clinically to diagnose neurodegenerative diseases
t-tau in CSFWithin 2 hours prior to tracer injectiont-tau (total tau) is significantly increased in the cerebrospinal fluid of patients with neurodegeneration and is one of the biomarkers used clinically to diagnose neurodegeneration
p-tau in CSFWithin 2 hours prior to tracer injectionp-tau (tau phosphorylated at Thr-181) is significantly increased in the cerebrospinal fluid of patients with neurodegeneration and is one of the biomarkers used clinically to diagnose neurodegeneration
NfL in CSFWithin 2 hours prior to tracer injectionNfL (neurofilament light chain) is significantly increased in the cerebrospinal fluid of patients with neurodegeneration and is one of the biomarkers used clinically to diagnose neurodegeneration
NfL in the bloodWithin 2 hours prior to tracer injectionNfL is significantly increased in the blood of patients with neurodegeneration and is one of the biomarkers used clinically to diagnose neurodegeneration

Countries

China

Contacts

Primary ContactShaobo Yao, PhD
yaoshaobo008@163.com86-0591-87981618

Outcome results

None listed

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