You also spammed all week-end, u just forgot today was a holiday:) Geniuses! Plitheone, u also said this was going to 1$... must be IMMINENTLY, right? Too bad u losers ruin this board, lmnl if they deliver only on the riplazym partnership is going at least 3x from here, and a lot more on the FDA approval. But thats why u are here...buying other people shares.
RE:BLA
U know what,i agree! And i agree with the odds u suggested.... these 2 owners are at helm since around 1 year and control 85% of all shares (!) , lets see what happens...
Steve33 wrote:
Its hard to be hopeful with the disastrous track record of this company. What I am feeling positive about is the BLA. They have spent two years on this with a new hired consultant for auditing. The product has no issues whatsoever. The company thrives with approval and is dead without it. But the odds are in our favour. 90% chance of approval in my mind or higher. The worst part is waiting for the submission. Surely it is soon as I believe Galbraith hinted as much two times during the meeting.
-----------------------
Facts are money is not a problem + riplazym partnership is
IMMINENT: LMNL just told you riplazym as been tested running in plant for 6 months, its a success. They met the FDA to submit and we're in may... plenty of time til end of june. Thats 2020 like they said in MDA! They can only say it that way. Same for partnership (next weeks), this is going to be a money printing machine... im sur we'll find a distributer with $$$;) By the way, the riplazym partnership will come with upfront money too.
6 months of cash, then SALP credit line if needed, THOMVEST owns lmnl, they finance companies like lmnl all the time if needed, money not a problem here...look at their website and all the businesses they manage, they know exactly what they are doing, owning 85% of all shares in lmnl. This quarter was not about money/revenue as u know at this point... but short term news. Thats why we are here;) And why the spammers spent all week-end onthis board.
"2020 remains an important and eventful year for the Company. While there are uncertainties for the year ahead, we remain focused on the resubmission of our Biologic License Application, or BLA to the Food and Drug Administration, or FDA for Ryplazim® (plasminogen), or Ryplazim® as a treatment of patients with congenital plasminogen deficiency, and the development of our small molecule pipeline . We also continue to plan and explore alternatives for the commercial launch of Ryplazim®, initially in the United States, if approved. We will continue to monitor and provide more updates as the situation unfolds."