Thanks for responding. I was asking "for what?" in response to the assertion that we were "Waiting for RBL" and you're right to point out that "The RBL ought to be finishing the data for prepublication." From an investor relations and a third party scientific verification standpoint that pre-print is important. But what I really wanted to know was how the RBL plays into the timing of the IND application. I could be mistaken but I don't recall the subjects of pre-prints and peer review coming up as contingencies prior to any of the handful of INDs that the Company has submitted in the past.
Does the FDA need something that the RBL has yet to provide in order to review an IND application or, if not, what information might still be needed in order to apply?