I still expect RVNC to announce the FDA's acceptance of the sBLA (and the PDUFA date) in an all-in-one PR that also sets forth the company's clinical and financial guidance for 2023.
If there were any issues, would disclosure be required?
The only "issue" at this stage of the sBLA would be an RTF letter, which would definitely require disclosure by RVNC.
“The efficient-market hypothesis may be the foremost piece of B.S. ever promulgated in any area of human knowledge!”