I think the FDA saw what they needed to see already with the experts meeting and are just going to start working with us mid-September dropping the hold and giving us the direction forward. They just want us to submit the paper work on what was agreed to and we will be able to use LL on EUA or whatever during any trial unlike what they did with us on CD10 and CD12.

I think this last meeting was to indicate the old help Gilead game is over and things will move real fast this Fall.