The wording change was not necessary, but is nice to see. Yes likely had to do with aligning to prominent previous trials like lecanemab.
Our endpoint selection was good, in line with regulatory expectations and current AD research norms. Will be great to see what our 2b/3 trial shows. 500+ patients, while relatively small on its own, is reliable enough for the volatility of these endpoints over almost 12 months to show some credible signal.