realstocky wrote: upon FDA ok! And we also agree on the value of the voucher +- 100M$ which 70% goes to LMNL! See we can all be friends... as for the inspection of the facility, i double Kedrion would of made that deal if it wasnt done or of it didnt think we would get the green light... we will soon know bud:) The more friends the better... xx ( on the cheek ):)
we're getting about 100M$ first week of june...
market cap is around that at the moment. Think about it means sp wise, and buy your shares if u see it. Next is pbi4050 that they will partner... thats worth 10x more than riplazym....
i have no problem buying at these levels and holding until the first week of june. I estimate the risk low as FDA already reviewed riplazym and it was no problem, only asked for more check points. We're at stage to place your bets, big players did 2 days ago where the sp hit near 5$, first week of june trading could be 10 to 15$...on FDA ok....
FDA granted ALREADY ORPHAN STATUS to riplazym... voucher with FDA ok will be worth around 120M$ automatically 1st week of june....we get 70% of that, Kedrion takes care of everything else, commercialisation, expenses etc,
+17M +5M, total value of deal is more than 100M$ to LMNL. (NR yesterday)
106M$ inflows to LMNL...
As usual do your dd. Dont listen to anyone on stockhouse boards.
Through its’ US subsidiary, Prometic Biotherapeutics Inc., the Company has resubmitted a BLA in September 2020 with the FDA seeking approval to treat patients with C-PLGD. The FDA confirmed that the resubmission is a complete, Class 2 response to the complete response letter issued in 2018 and has provided a Prescription Drug User Fee Act (“PDUFA”) target action date of June 5, 2021.
Ryplazim® has previously been granted Orphan Drug and Rare Pediatric Disease Designations by the FDA for the treatment of congenital plasminogen deficiency. ====>voucher:)
--------------------------------------
https://www.marketbeat.com/stocks/NASDAQ/LMNL/price-target/
----------------------------------------------------------------------------------------------------------------------
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.