Given many of the pediatric Rett patients are from Australia, and the fact that the Rett Syndrome Association of Australia is a huge supporter of Anavex, maybe we should also go the route of the EMA for a Rett approval.
Hi Gary--great to see you here on this forum as we spent a lot of years together back on the IMGN IV board. Your first post was a good one. It offers a credible reason why AVXL did not file a Form 8-K when the EXCELLENCE top line data was released; that is, AVXL is leaving the door open for possible regulatory approval irrespective of the failed trial endpoints.