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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

Post by stockbuphoonon Jul 20, 2021 11:48am
28 Views
Post# 33575364

Liminal Business Milestones & Cash - facts only

Liminal Business Milestones & Cash - facts only Q1 2021 Results Slides (liminalbiosciences.com)

At March 31, 2021: •
Cash & cash equivalents: CAD 21.6M,  Net loss: CAD $20.5M Admin, selling & marketing expenses (highest): $6.7M, Plasma div: $6.0M, Small molecule $5.5M, Financing $2.4M 
Thus, burn is $20M per qtr so their cash is gone by end of June but they received $17M cash for plasma collection centres and $5M for plasma division (another quarter of cash) 

Liminal - Product Pipeline (liminalbiosciences.com) - no link to any further Fez/4050 activities

Milestones as noted in Q1 2021 presentation 


Potential monetization of PRV, if granted by FDA on successful BLA approval - 2021 

Fezagepras Phase 1 multiple ascending dose (MAD) study in the United Kingdom in healthy 
volunteers Ongoing ------- nothing more said since end of May

Anticipated initiation of a global Phase 2b clinical trial in patients with idiopathic pulmonary fibrosis (IPF) subject to the results of the phase 1 study H1-2022 ------- cancelled with little explanation!!! HUGE drop in price targets to $4.50

Preparatory work for anticipated Phase 1b/2a clinical trial of fezagepras in the US for patients with high triglyceride levels (hypertriglyceridemia) 2022 ------ cancelled!!! Liminal never shared any market potential so it was not included in price targets

GPR84 antagonist Initiate a pre-clinical IND enabling program to support a First-in-Human Phase 1 single ascending dose clinical trial of our GPR84 drug candidate in healthy volunteers for safety and tolerability TBC ------ no dates as it needs to finish preclinical trials and then work with FDA to apply for IND application

OXER1 antagonist Initiate a pre-clinical IND enabling program to support a First-in-Human Phase 1 single ascending dose clinical trial of our OXER1 drug candidate in healthy volunteers for safety and tolerability TBC ------ no dates as it needs to finish preclinical trials and then work with FDA to apply for IND application

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