realstocky wrote:
already peaked on nasdaq at 43$ CAN.... They added the checkpoints, the plant is obviously set
Liminal went through 6 months of CMC testing at their Ryplazim manufacturing plant as part of BLA after years and years of producing in Laval for over 5000 doses of administered Ryplazim. Any Rockville expertise had been transferred long ago to Laval.
(( they ran the plant 6 months, ran batchs etc )) BLA riplazym submission this quarter + partnership distribution for it this quarter.
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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
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)
Kenneth Galbraith, CEO
Liminal BioSciences (NASDAQ, TSX:LMNL) is undergoing a significant strategic transformation to simplify its operations, achieve financial stability and focus R&D on small molecule therapeutics.
“This is a refresh of ProMetic Life Sciences, which was around for 25 years, but stumbled after a series of setbacks and was left with a crushing debt burden and interest payments,” CEO, Kenneth Galbraith, says in an interview with BioTuesdays.
New and existing investors arranged a major equity financing in the second quarter of 2019, strengthened the executive team and board, changed Prometic’s name and achieved a NASDAQ listing in November.
Liminal also sold its chromatography and bioprocessing business to investment giant, KKR, for some $80-millon in 2019, with $50-million in proceeds on closing. “The sale of the division will advance our transition to a new focus on small molecule therapeutics and strengthen our financial position,” he adds.
Mr. Galbraith explains that Liminal’s current R&D focus is a small molecule therapeutics group for the treatment of serious fibrosis in respiratory, liver and kidney disease, with expected expansion of the R&D portfolio through collaboration, in-licensing and acquisition.
In addition, the company plans to file an amended biologics license application for priority review with the FDA in the first half of 2020 for approval of Ryplazim for the treatment of congenital plasminogen deficiency, a rare disorder that results in inflamed growths on the mucous membranes that line body openings, such as the eyelids and the inside of the mouth. A European filing for Ryplazim is planned after potential approval and launch in the U.S.
Type 1 plasminogen deficiency (PLGD) is an ultra-rare genetic disease
Liminal is in talks to sign a global marketing partnership for Ryplazim to further strengthen its financial position. Under the accord, Liminal expects to continue manufacturing Ryplazim to supply its commercial partner. Additional indications for Ryplazim provide market expansion opportunities, such as acute wound healing.
Mr. Galbraith points out that as part of its strategy to build a portfolio of antifibrotics, Liminal’s research has focused on mechanisms of G-protein coupled receptors and compounds with multi-targeting effects and roles in inflammation, metabolic disease and fibrosis.
“Our discovery engine has generated more than 3,000 proprietary compounds with a multi-target effect against free fatty acids and other receptors,” he added. “And robust activity in a broad panel of in vivo disease models has been confirmed in more than 30 compounds.”
According to Mr. Galbraith, Liminal’s lead anti-inflammatory and anti-fibrotic agent, Fezagepras (formerly PBI-4050), is designed to reduce fibrosis via regulation of macrophages, fibroblasts or myofibroblasts, and epithelial cells. In preclinical studies, Fezagepras has demonstrated activity in models of chronic and diabetic kidney disease; lung, liver and heart fibrosis; Crohn’s disease; scleroderma; and osteoporosis.
Fezagepras has been evaluated in more than 250 subjects, dosed up to 1,200 mg daily, in eight clinical trials. Most adverse events were mild.
“Our lead indication for Fezagepras going forward is Alstrm syndrome, a rare condition that affects many body systems. Mr. Galbraith notes that fibroblasts with mutations in the ALMS1 gene are resistant to apoptosis and secrete high levels of extracellular matrix.
Many of the signs and symptoms of the disorder begin in infancy or early childhood. Alstrm syndrome is characterized by progressive and severe fibrosis, affecting the heart, kidneys, lungs and liver. Childhood onset involves visual dysfunction, hearing loss, obesity and diabetes. Patient life expectancy rarely exceeds 50 years of age.
Industry estimates suggest 1,200 individuals with Alstrm syndrome have been identified worldwide and there is no FDA or European Medicines Agency (EMA) approved treatment for these patients. Fezagepras has both orphan drug designation and rare paediatric disease designation from the FDA; orphan drug status from the EMA; and promising innovative medicine status in the UK for Alstrm syndrome.
In an earlier Phase 2 trial with 12 patients, which was the largest study ever conducted in this patient population, Fezagepras had a dramatic impact on fibrosis in multiple organ systems. “Some of these patients have been studied for almost two years and we’re getting a pretty good data set on long-term use of the drug,” Mr. Galbraith says.
Liminal has met with regulators about a Phase 3 trial of Fezagepras, with final meetings scheduled for 2020 with the FDA and EMA to set the protocol and primary endpoints for a pivotal trial.
The company hopes to start the trial in the second half of 2020 at three clinical sites in the U.S., UK and Italy. Patient identification for study is underway, with a projected goal to enroll about 45 Alstrm syndrome subjects – 30 adults and 15 paediatric patients – treated with 1,200 mg of Fezagepras dosed once daily.
Patients will come to the central sites for screening and imaging, go home with their medication and return to a central site every six months for imaging and scanning.
“Our goal is to reduce fibrosis in organ systems to allow these patients to live longer, without the need for organ transplants and other requirements to manage their disease,” Mr. Galbraith says. “We are also working with well-established international Alstrm patient advocacy organizations to assist in conducting the study.”
Given the small size of the market, Mr. Galbraith figures the company would build a small regional sales and marketing infrastructure, if Fezagepras is approved.
Liminal also has developed a second drug candidate, PBI-4547, as an analogue of Fezagepras, with a differentiated mechanism for treating liver fibrosis.
In preclinical studies, with a high-fat diet mouse, PBI-4547 improved glucose metabolism and insulin resistance, and reduced liver damage. In an obese mouse model, PBI-4547 reversed diabetes and metabolic syndrome through regulation of lipid/ glucose metabolism, beta-oxidation and fibrosis in liver and white adipose tissue. And in a carbon tetrachloride liver fibrosis mouse model, PBI-4547 reduced the collagen content and level of liver fibrosis, Mr. Galbraith points out.
“We think PBI-4547 can be beneficial treating patients with non-alcoholic steatohepatitis (NASH) and, in NASH, we’re interested in treating not only fibrosis in the liver that has developed over time from having NASH, but also fatty liver disease, which is a precursor of fibrosis. We’re also interested in regulating certain metabolic conditions, such has improving insulin sensitivity and triglyceride levels, for example. We see PBI-4547 as an anti-fibrotic, anti-inflammatory, with an impact on metabolic disorders,” he adds.
Liminal hopes to complete its Canadian Phase 1 study with PBI-4547 in 2020 and then, depending on the results, move into a global Phase 2 trial.
“We have a lot on the drawing board both short- and long-term, including putting something in the clinic for kidney disease, studying novel targets and pathways beyond free fatty acid receptor biology and expanding our current drug discovery engine with novel technologies, such as AI and machine learning.”
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To connect with Liminal, or any of the other companies featured on BioTuesdays, send us an email at editor@biotuesdays.com.
LMNL
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LMNL just rented 4000 sq in Sawston...
Something big is coming, wouldnt surprise me if these spammers heard about it. Keep your shares like the owners.
Liminal BioSciences chooses Iconix 1 at Unity Campus as base for future growth
Cambridge-based property developer and investor Howard Group is delighted to announce that Iconix Park at Unity Campus in Sawston is now fully let, having agreed a five-year lease for 3,985 sq ft of space within the Iconix 1 building to Liminal Biosciences.
Liminal BioSciences (formerly Prometic Life Sciences) is a global biotechnology company specialising in discovering, developing and commercialising novel small molecule compounds for respiratory, liver and renal diseases; with a specific focus on developing solutions for rare and orphan diseases.
Ideally positioned within the vibrant Cambridge life science and technology cluster, Iconix Park is already home to a number of innovative science and knowledge intensive business. Liminal BioSciences completes an already impressive occupier list at the Park, which includes Biocair, Iontas, AQDot and Telensa.
With aspirations for rapid growth; positioning within the cluster, the aggregation of like-minded businesses in the area, access to the talent base and the future potential to expand within the wider Unity Campus estate were all critical factors in Liminal Biosciences’ decision to choose Iconix Park as its Cambridge base.
Colin Brown, Director - Development, Howard Group (pictured), commented: “We are delighted to welcome Liminal BioSciences to Iconix Park at Unity Campus. Attracting yet another innovative, rapidly growing knowledge-intensive organisation is testament to the successful integration of Iconix Park and Unity Campus into the wider Cambridge science and technology cluster. Our position, just four miles south of the Cambridge Biomedical Campus and close to other leading research facilities, coupled with our flexible and quality driven approach to development, has enabled us to secure an exciting and innovative occupier base, which appreciates the ‘downstream’ opportunities that our further development of Unity Campus will unlock as their own organisations evolve and grow.”
Howard Group acquired Iconix Park in 2013, having first purchased Sawston Trade Park in 2009 as part of its commitment to investing in and around the city of Cambridge. The purchase of Iconix Park included additional development land between the two estates. Further to a holistic master planning exercise, Unity Campus was created to encompass all of Howard Group’s Sawston assets. The Campus will bring together the office and laboratories of Iconix Park with new, high quality business and R&D accommodation on the adjacent land. The first phase of this development, The Works, is now complete and provides a total of 63,000 sq ft of flexible modern business space with suites available from 7,500 sq ft.
Discover more about Unity Campus and The Works
Howard Group is an established and successful property and capital investment business based in Cambridge with interests throughout the South East.