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Liminal BioSciences Inc. PFSCF


Primary Symbol: 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 Arrakis37on Jul 24, 2020 2:12pm
47 Views
Post# 31315653

RE:nasdaq will see the sp appreciate hugely, hit intraday 43$CA

RE:nasdaq will see the sp appreciate hugely, hit intraday 43$CA

Promises, Promises, Promises... since a quarter of a century.

nothing substantial.

Was 43$ 2 weeks ago blablabla
...anticipated, expected, conditional, will be, could be, must be, blablabla 

SHOW ME THE MONEY.

ah ? No money ?

made 131% YTD with other incredible stocks.  I've shorted only this one.  Guess why ?

Because it's OBVIOUS that's a scam.

Reality check here : NOTHING IS COMPLETE.

Dilution is coming.

Investors, analysts, institutionals and even lead scientists are GONE.

Try to contact Liminal, you'll see.

That's the reason why FDA approval is not coming.

The end.


realstocky wrote: 2 weeks back... Just ignore these clones, arakis/plitheone/gob,  deranged individuals that cant rationalise losing money...instead they ruin everybody else lifes out of revenge. What goes around comes around though...

LMNL completed 100% the check points as asked by the FDA, now they will submit riplazym as detailed below, FDA already reviewed riplazym and passed conditional on those check points being set. They are set, resubmission is basically a formality. The 2 owners indeed own 85% of all shares, stay tuned:"In early 2019 the Company established the following critical path towards regulatory approval for RyplazimTM in the U.S. is as follows:

 


1. Development and validation of new analytical assays and in-process controls (complete)
2. Finalization of PPQ protocol (complete)
3. Manufacturing of additional conformance lots (complete)
4. Fill & Finish at external Contract Manufacturing Organization (“CMO”) (complete)
5. Data analysis & preparation of required documents for FDA (in process)
6. Regulatory filing of BLA amendment documents – now likely to take place in H1 2020 ( updated to this quarter)
7. Anticipated new PDUFA date after the acceptance of the amended BLA"

Anticipated Key Milestones (from corp. slides)


1H-2020Expected commercial partnership for Ryplazim™ ( H1 updated to this quarter )

1H-2020Expected filing of amended BLA with FDA for Ryplazim™ (priority review expected)



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