Liminal BioSciences Presents Two Case Histories on Investigational Intravenous Plasminogen (Human) Replacement Therapy at The ASH Conference

December 7, 2020 Shrinal Inamdar

LAVAL, CANADA, and CAMBRIDGE, ENGLAND – December 7, 2020 – Liminal BioSciences Inc. (Nasdaq: LMNL) (“Liminal BioSciences” or the “Company”), a clinical-stage biopharmaceutical company, today announced the presentation of two scientific posters with individual case report data highlighting potential activity of intravenous Ryplazim® (plasminogen) on infertility and acute airway obstruction in patients with congenital plasminogen deficiency (“C-PLGD”). Results were presented during the 62nd American Society of Hematology Annual Meeting and Exposition.

Two posters were presented that highlighted individual case histories of patients with C-PLGD treated with the investigational intravenous Ryplazim® (plasminogen) in compassionate use and expanded access cases. The first poster was a case of a previously infertile female patient having a successful pregnancy.  The second poster reported 4 cases of acute respiratory distress with successful resolution of airway obstruction.

“This data related to treatment with investigational plasminogen replacement shows promise as a potential therapy to target the many life-altering and potentially life-threatening systemic manifestations of congenital plasminogen deficiency through intravenous plasminogen (human) replacement therapy”, stated Bruce Pritchard, Chief Executive Officer. “These data highlight the potential impact for the treatment of congenital plasminogen deficiency in two areas that can present significant challenges for patients caused by plasminogen deficiency.

Both poster presentations were also published in the November supplemental issue of the peer-reviewed journal Blood along with a Comprehensive Case Review entitled ‘Painting the Clinical Picture Of Congenital Plasminogen Deficiency (C-PLGD) through A Comprehensive Case Study Review’.

The poster presentations are entitled:

  • Successful Pregnancy in A Patient with Infertility Due To Congenital Plasminogen Deficiency Treated With Intravenous Plasminogen (Human) Replacement Therapy
  • Acute Airway Obstruction in 4 Pediatric Patients with Congenital Plasminogen Deficiency (C-PLGD) Treated with Intravenous Plasminogen (Human) Replacement Therapy Under an Expanded Access Protocol

This is the only reported case of a patient with C-PLGD and documented infertility who was being treated with investigational intravenous plasminogen (human) replacement therapy in the Phase 2/3 clinical trial and subsequently became pregnant. Treatment with plasminogen was continued throughout the pregnancy following agreement with both the national regulatory and study ethical review. The pregnancy was successful, and the patient delivered a healthy child.

In the case series of acute airway obstruction, Dr. Charles Nakar of Indiana Hemophilia And Thrombosis Center who presented the poster, concluded that “these cases demonstrate the potential for IV plasminogen concentrate replacement therapy to provide rapid regression and prevent respiratory failure and potential serious sequalae in C-PLGD patients with airway involvement due to fibrinous lesions.”

Copies of these scientific posters are available from the Company’s website at


About Liminal BioSciences Inc.

Liminal BioSciences is a clinical-stage biopharmaceutical company focused on discovering, developing and commercializing novel treatments for patients suffering from diseases of high unmet medical need, primarily related to fibrosis, including respiratory, liver and kidney diseases. Liminal BioSciences has a deep understanding of certain biological targets and pathways that have been implicated in the fibrotic process, including fatty acid receptors such as FFAR1, G-protein-coupled receptor 84 (GPR84), and peroxisome proliferator-activated receptors (PPARs). Our lead small molecule product candidate, fezagepras (PBI-4050), is expected to enter a Phase 1 clinical trial in Q4-2020 in the UK to evaluate multiple ascending doses in normal healthy volunteers, at daily dose exposures higher than those evaluated in our previously completed Phase 2 clinical trials. Fezagepras is expected to be further evaluated in a global Phase 2b clinical trial in patients with idiopathic pulmonary fibrosis (IPF) anticipated to be initiated in H2-2021. In addition, we expect to initiate a Phase 1b/2a clinical trial of fezagepras, likely in the US, for patients with high triglyceride levels (hypertriglyceridemia) in H2-2021.

Fezagepras has previously been granted Orphan Drug Designation by the FDA and the European Medical Agency (EMA) for the treatment of IPF. The treatment has also received a Promising Innovative Medicines (PIM) designation by the Medicines and Healthcare products Regulatory Agency (MHRA) for IPF.

Liminal BioSciences has also leveraged its experience in bioseparation technologies through its subsidiary Prometic Bioproduction Inc. to isolate and purify biopharmaceuticals from human plasma. Liminal BioSciences’ lead plasma-derived product candidate is Ryplazim®(plasminogen) (“Ryplazim®”), for which the Company, through its US subsidiary, Prometic Biotherapeutics Inc., resubmitted a BLA in September 2020 with the FDA seeking approval to treat patients with congenital plasminogen deficiency. The PDUFA target action date for this BLA filing is 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.

Prometic Plasma Resources, a subsidiary of Liminal BioSciences, has joined the CoVIg-19 Plasma Alliance to contribute to the acceleration of the development of a potential new therapy for COVID-19. Liminal BioSciences’ Canadian plasma collection center located in Winnipeg, Manitoba is licensed by the FDA and Health Canada, and is certified by the European Union and the Plasma Protein Therapeutics Association. Liminal BioSciences’ American plasma collection center located in Amherst, New York is licensed by the State of New York and its BLA submission is currently under review by the FDA.

Liminal BioSciences has active business operations in Canada, the United Kingdom and the United States.


Forward Looking Statement

This press release contains forward-looking statements about Liminal BioSciences’ objectives, strategies and businesses that involve risks and uncertainties. Forward‐looking information includes statements concerning, among other things, statements with respect to the timing for FDA review of the BLA for Ryplazim®, the potential of our product candidates and development of R&D programs and the timing of initiation of clinical trials.

These statements are "forward-looking" because they are based on our current expectations about the markets we operate in and on various estimates and assumptions. Actual events or results may differ materially from those anticipated in these forward-looking statements if known or unknown risks affect our business, or if our estimates or assumptions turn out to be inaccurate. Among the factors that could cause actual results to differ materially from those described or projected herein include, but are not limited to, risks associated with FDA review, our ability to effectively establish a commercial organization, Liminal BioSciences’ ability to develop, manufacture, and successfully commercialize product candidates, if ever, the impact of the COVID-19 pandemic on its business operations, clinical development, regulatory activities and financial and other corporate impacts, the availability of funds and resources to pursue R&D projects, the successful and timely completion of clinical trials, the ability of Liminal BioSciences to take advantage of business opportunities in the pharmaceutical industry, uncertainties associated generally with research and development, clinical trials and related regulatory reviews and approvals and general changes in economic conditions. You will find a more detailed assessment of these risks, uncertainties and other risks that could cause actual events or results to materially differ from our current expectations in the filings the Company makes with the U.S. Securities and Exchange Commission and Canadian Securities Commissions filings and reports filings and reports, including in the Annual Report on Form 20-F, as amended,  for the year ended December 31, 2019 and future filings and reports by the Company, from time to time. Such risks may be amplified by the COVID-19 pandemic and its potential impact on Liminal BioSciences’ business and the global economy. As a result, we cannot guarantee that any forward-looking statement will materialize. Existing and prospective investors are cautioned not to place undue reliance on these forward-looking statements and estimates, which speak only as of the date hereof.  We assume no obligation to update any forward-looking statement contained in this Press Release even if new information becomes available, as a result of future events or for any other reason, unless required by applicable securities laws and regulations.


For further information please contact:

Corporate Contact                           

Shrinal Inamdar

Manager, Investor Relations and Communications

+1 450.781.0115


Media Contact

Kaitlin Gallagher

+1 212.253.8881    





Previous Article
Liminal BioSciences Announces First Subject Dosed in Phase 1 Multiple Ascending Dose Clinical Trial of Fezagepras
Liminal BioSciences Announces First Subject Dosed in Phase 1 Multiple Ascending Dose Clinical Trial of Fezagepras

LMNL today announced that the first subject has been dosed in the Company’s fezagepras Phase 1 multiple asc...

Next Article
Liminal Biosciences to Present at The Stifel Virtual Healthcare Conference
Liminal Biosciences to Present at The Stifel Virtual Healthcare Conference

LMNL is scheduled to present a company overview at The Stifel 2020 Virtual Healthcare Conference on Monday ...

Go to Liminal BioSciences Q2 2021 Results Conference Call

View Now