Clinical trial · NCT06723015 · ENROLLING_BY_INVITATION · PHASE2
Tau PET Outcomes With Anti-amyloid Immunotherapies
Sponsor: Mayo Clinic
Summary
This is an imaging study of patients with mild Alzheimer's disease receiving amyloid-targeting therapy and under the care of neurologists at Mayo Clinic in Rochester, MN.
Interventions
- 18F-AV-1451 · DRUG
Subjects will receive two Tau PET (18F--AV-1451) brain scans with approximately 10 mCi (370 MBq) (+/- 10%mCi) of 18F-AV-1451. Images will be collected for a 20-minute acquisition between 80-100 minutes after injection. Tau PET scans will occur at baseline and 12-18 months after completing anti-amyloid immunotherapy treatment..
Published eligibility criteria
Verbatim from the registry. Only the site can decide how these apply to a specific patient.
Inclusion Criteria * Age 50-90 years * Male or female * Mild cognitive impairment due to AD or mild AD * Amyloid positive via CSF or PET * Meets other eligibility criteria for anti-amyloid immunotherapy * Subject or delegate provides informed consent Exclusion Criteria * Subjects unable to lie down without moving for 10 minutes. * Women who are pregnant or cannot stop breast feeding for 24 hours. * Claustrophobic patients unable to tolerate the scans (no sedation can be offered).
Sites (1)
- Mayo Clinic, Rochester, Minnesota
Not medical advice. Trial0 is a navigation service, not a medical provider. Nothing here is medical advice or a recommendation to pursue any treatment; eligibility matching is informational, based on published registry criteria, and only the trial site or treating clinician can determine actual eligibility. Decisions belong with the patient and their own doctors. Registry data refreshed at most hourly; last update posted 2025-11-18.