Join today and have your say! It’s FREE!

Become a member today, It's free!

We will not release or resell your information to third parties without your permission.
Please Try Again
{{ error }}
By providing my email, I consent to receiving investment related electronic messages from Stockhouse.

or

Sign In

Please Try Again
{{ error }}
Password Hint : {{passwordHint}}
Forgot Password?

or

Please Try Again {{ error }}

Send my password

SUCCESS
An email was sent with password retrieval instructions. Please go to the link in the email message to retrieve your password.

Become a member today, It's free!

We will not release or resell your information to third parties without your permission.

Liminal BioSciences Inc. LMNL

Liminal BioSciences is a biopharmaceutical company focused on the discovery and development of novel, small molecule drug candidates for the treatment of patients suffering from fibrotic or inflammatory diseases that have a high unmet medical need. Liminal BioSciences operates on an integrated basis from our talent hubs in Laval, Quebec, Canada, and Cambridge, UK. Our common shares are listed for trading on the Nasdaq Global Market.


NDAQ:LMNL - Post by User

Comment by GunnerGon May 18, 2021 11:34pm
53 Views
Post# 33228000

RE:Payday will be 1st week of june with the FDA green light

RE:Payday will be 1st week of june with the FDA green lightI love how you keep moving the bar.

No 2x 3x with agreement, LOL.  Next failure, 1st week of June.


realstocky wrote:

We're at stage to place your bets, big players did yesterday 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...

 

 

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:)


 



<< Previous
Bullboard Posts
Next >>