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Liminal BioSciences Announces FDA Approval for its Biologics License Application for Ryplazim® (plasminogen, human-tvmh)

/PRNewswire/ - Liminal BioSciences Inc. (Nasdaq: LMNL) ("Liminal BioSciences" or the "Company") announced today that the U.S. Food & Drug Administration (FDA).

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Liminal BioSciences Announces FDA Approval for its Biologics License Application for Ryplazim (plasminogen, human-tvmh)

LAVAL, QC and CAMBRIDGE, England, June 4, 2021 /PRNewswire/ Liminal BioSciences Inc. (Nasdaq: LMNL) ("Liminal BioSciences" or the "Company") announced today that the U.S. Food & Drug Administration

United kingdomBioscience ryplazimKaitlin gallagherShrinal inamdarPrometic bioproduction incPrometic biotherapeutics incLaboratory abnormalitiesExchange commissionUs food drug administrationPrnewswire liminal biosciences incLiminal biosciences incDrug administrationImportant safety informationInfectious agentsCreutzfeldt jakob diseaseLiminal bioscience

Liminal Announces Voting Results of Its 2021 Annual and Special General Meeting of Shareholders (AGM)

/PRNewswire/ - Liminal BioSciences Inc. (Nasdaq: LMNL) ("Liminal BioSciences" or the "Company") announced the voting results from its Annual General and.

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(LMNL) - Liminal BioSciences To Offload Plasma Collection and Plasma-Derived Therapeutics Business To Kedrion

(LMNL) - Liminal BioSciences To Offload Plasma Collection and Plasma-Derived Therapeutics Business To Kedrion
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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 News provided by Share this article Share this article LAVAL, QC, and CAMBRIDGE, England, Dec. 15, 2020 /PRNewswire/ - Liminal BioSciences Inc. (Nasdaq: LMNL) ( Liminal BioSciences or the Company ), a clinical-stage biopharmaceutical company, today announced that the first subject has been dosed in the Company s fezagepras Phase 1 multiple ascending dose clinical trial in healthy volunteers. The new clinical trial is designed to look at more frequent daily dosing (twice and three times daily) of fezagepras up to 2,400mg for a total of 14 days. The clinical trial is a standard placebo-controlled Phase 1 ascending dose design in healthy volunteers. The clinical trial endpoints will include safety, pharmacokinetics, and exploratory biomarkers related to the mechanism of action of fezagepras. The data from this clinical trial will be used to guide selection of the app

New yorkUnited statesUnited kingdomState of new yorkBruce pritchardPrometic bioproduction incPlasma alliancePrometic biotherapeutics incRegulatory agencyEuropean medical agencyExchange commissionEuropean unionHealth canadaPlasma protein therapeutics associationLiminal biosciences incChief executive officer

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