Clinical trials

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Condition / disease
Location
Status: Recruiting

Evaluate the Concordance Between PET Imaging of [18F]-APN-1607 Injection and Postmortem Brain Tissue Tau Pathology in Individuals With HV and MCI or AD.

1. To evaluate the diagnostic performance of \[18F\]-APN-1607 injection PET imaging in detecting uptake patterns consistent with AD neuropathological changes as defined by the National Institute on Aging-Alzheimer's Association (NIA-AA) criteria. 2. To assess the association between \[18F\]-APN-1607 injection and Alzheimer's disease (AD)-related tau neurofibrillary pathology (as determined by post-mortem brain tissue histopathology), and detect the uptake pattern corresponding to neurofibrillary tangle (NFT) scores. 3. To evaluate the safety of \[18F\]-APN-1607 injection.

Participants needed: 12
Trial details
Phase: Phase 3Age: 50+Biological sex: AllType: InterventionalSponsor: JYAMS PET Research & Development LimitedUpdated: Aug 17, 2026Locations: 1
Eligibility criteria

Able to understand and voluntarily sign a written informed consent form (ICF). [+5]

Confirmed brain structural abnormalities that may affect PET reading, e.g., larg... [+7]

Status: Recruiting

Evaluate the Use of [18F]-APN-1607 PET in Subjects With AD-related Cognitive Impairment and Subjects With Normal Cognitive Function

This study is to evaluate the efficacy and safety of \[18F\]-APN-1607 Injection in PET imaging for detecting AD-related cognitive impairment.

Participants needed: 316
Trial details
Phase: Phase 3Age: 50+Biological sex: AllType: InterventionalSponsor: JYAMS PET Research & Development LimitedUpdated: Feb 20, 2026Locations: 2
Eligibility criteria

Subjects must be able to understand and voluntarily sign a written informed cons... [+4]

Specific clinical phenotypes of atypical AD as defined in the 2014 IWG-2 criteri... [+12]