The overarching goal of this trial is to assess whether icosapent ethyl beneficially affects intermediate physiological measures associated with onset of AD in order to evaluate whether larger, multi-site, longer-duration Alzheimer's prevention trials are warranted to assess more definitive clinical outcomes.
IF Brave EPA is successful ...the FDA may fast track a trial ..say the size of MITIGATE ....but to suggest that it's possible to grant approval based on Brave- EPA alone is really stretching it IMHO Kiwi