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Study Information

An open-label, non-randomized, multi-center pivotal Phase 3 study to evaluate the efficacy and safety of PET imaging with [18F]PI-2620 for the detection of tau deposition when compared to post-mortem histopathology


Inclusion Criteria

  •  Age: 50 and over
  •  Targets: Prognosis <12mo.
  •  AD MEDS: No amyloid or tau targeting therapies
  •  Clinical Trials: No amyloid or tau targeting studies unless proof of placebo can be provided.
  •  Study Partner: Required
  •  Mechanism of Action: Next-generation positron emitting radiopharmaceutical for specific and sensitive in vivo detection of tau protein aggregates in the brain.

Exclusion Criteria

  • Neurological Disease History: Structural brain lesions >2cm. Encephalopathy due to EtOH or end-stage liver disease
  • Cancer History: N/A
  • Geriatric Depression Scale: N/A
  • HIV, HepB or HepC: N/A
  • C-SSRS: N/A
  • Alcohol or Drug Abuse: N/A
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