Evaluation of Imaging Characteristics of [18F]PI-2620 PET in AD and PSP Patients Using High and Low Specific Activity

PHASE1CompletedINTERVENTIONAL
Enrollment

10

Participants

Timeline

Start Date

November 12, 2020

Primary Completion Date

October 26, 2022

Study Completion Date

October 26, 2022

Conditions
Alzheimer DiseaseProgressive Supranuclear Palsy
Interventions
DRUG

[18F]-PI2620

\[18F\]PI-2620 is a radioactive diagnostic agent being developed for the indication of PET imaging of the brain to detect tau pathology in adult patients who are being evaluated for neurodegenerative decline. All patients will receive two administrations of \[18F\]PI-2620 at a radioactive dose of 185 MBq, one with high specific activity (≤ 5 µg tracer mass dose), another one with low specific activity (40-50 µg tracer mass dose).

Trial Locations (1)

Unknown

Department of Nuclear Medicine, University Hospital Leipzig, Leipzig

Sponsors
All Listed Sponsors
collaborator

Life Molecular Imaging SA

INDUSTRY

lead

Life Molecular Imaging GmbH

INDUSTRY

NCT04715750 - Evaluation of Imaging Characteristics of [18F]PI-2620 PET in AD and PSP Patients Using High and Low Specific Activity | Biotech Hunter | Biotech Hunter