RE:RE:RE:RE:RE:the very troubling case of the Zenith IP "issue"...
bear, i hope everyone reads the framework that is on SEDAR...assuming you have read it are there any "flys" to worry about...my read just reinforced my belief that BOM will start (1st patient dosed to eliminate "mealy mouthing" that comes from RVX on this matter) in 2016..one thing i worry about is what CFDA is like to deal with... whereas the FDA has a 208 history the CFDA is coming in cold and to approve a piii cold after a failed PII may be somewhat more complicated but who knows for sure as IMO bigger issue is always Chinee is commy and so it may get approved with a right call or never be approved...regards