he's being on record so he's covering all bases, we all know if we dont get the FDA green light, riplazym is done. But odds are we'll be fine, read below:

Next:1- FDA riplazym approval 2- riplazym distribution deal 3- priority voucher potentially worth 120million$ or more... market cap is also around 120M$....

:::

 FDA already reviewed riplazym and it was no problem, only asked for aditional check points... i think this time we'll get it!  LMNL also hired a quality assurance specialist moira daniels, i bet to please the FDA.

 

conference call info from weeks ago

" I think it's without giving anything away on what we're doing with negotiations and discussions that would be commercially sensitive. The reality is that we are looking at all opportunities here, whether we do this before or after Ryplazim approval. "<<<< =================

 

incoming........$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$

=================================================================

 

confirmed as well on latest NR

PDUFA target action date of June 5, 2021 for Ryplazim

"2021 has the potential to be a transformative one for Liminal BioSciences as we progress our evaluation of strategic alternatives for our plasma-derived therapeutics business, while continuing to work towards the PDUFA target action date of June 5, 2021 for Ryplazim ® (plasminogen)," stated Patrick Sartore , President of Liminal BioSciences.