Is it possible that we don’t have all the data and the FDA requested the small sub set of the data first just from critical group ? Maybe it was easier to get that first and talk about that group of individuals first ? I mean the FDA requested the data right. So why wouldn’t they request what they want which sounds like the worst of the worst.

I just thought about this earlier due to the fact that NP sent out that email. Not sure it’s legit but it looks like it ? This seems like the most logical answer and the best way to get EAU until a phase 4 can be completed.