AC Immune’s PI-2620 Tau-PET Diagnostic in Phase 3 Receives Fast Track Designation in Three Neurodegenerative Conditions
AC Immune’s PI-2620 Tau-PET Diagnostic in Phase 3 Receives Fast Track Designation in Three Neurodegenerative Conditions
- PI-2620 is in Phase 3 development in Alzheimer’s disease by AC Immune’s partner, LMI
- This Fast Track designation applies across Alzheimer’s disease, progressive supranuclear palsy, and corticobasal degeneration
- Follows two previous Fast Track designations for ACI-35.030 and ACI-24.060 active immunotherapies
- Affirms AC Immune’s leadership and commitment to bringing precision medicine to the management of neurodegenerative diseases
Lausanne,
Fast Track designation for [18F]PI-2620 has been granted for clinical development in Alzheimer’s disease (AD), progressive supranuclear palsy (PSP), and corticobasal degeneration (CBD).
The FDA’s Fast Track program is designed to accelerate the development and review of drugs that address serious conditions and fulfill unmet medical needs. This designation underscores the broadening view in the medical community that early and accurate diagnoses of neurodegenerative disease may lead to improved outcomes, thanks to emerging treatments.
PI-2620 is a next-generation PET imaging agent currently in Phase 3 clinical development for detecting Tau pathology in Alzheimer's disease. The compound is also being investigated in other neurodegenerative diseases by many academic researchers and in drug development trials. Tau proteins are a hallmark of several neurodegenerative disorders including AD, PSP, CBD, and frontotemporal lobar dementia (FTLD), and accurately imaging the pathology could significantly enhance disease diagnosis and improve patient care.
Dr. Andrea Pfeifer, CEO of
About PI-2620
PI-2620 was discovered and developed as part of a research collaboration between
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