Last update 08 May 2025

Plasminogen(Omnio AB)

Overview

Basic Info

Drug Type
Enzyme
Synonyms-
Target
PLG
Action
modulators
Mechanism
PLG modulators(Plasminogen modulators)
Therapeutic Areas
Nervous System DiseasesCardiovascular DiseasesEndocrinology and Metabolic Disease+ [2]
Active Indication
Diabetic FootEar Diseases
Inactive Indication
Plasminogen Deficiency, Type I
Originator Organization
ProMetic Biotherapeutics Ltd.
Active Organization
Omnio ABOmnio ABLiminal BioSciences, Inc.Liminal BioSciences, Inc.
Inactive Organization
ProMetic Biotherapeutics Ltd.
License Organization-
Drug Highest PhasePhase 2
First Approval Date-
Regulation-
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Structure/Sequence

Related

2
Clinical Trials associated with Plasminogen(Omnio AB)
NCT02690714
/ CompletedPhase 2/3
A Phase 2/3, Open-Label, Repeat-Dose Study of the Pharmacokinetics, Efficacy, and Safety of Prometic Plasminogen Intravenous Infusion in Subjects With Hypoplasminogenemia
NCT02312180
/ CompletedPhase 1
A Phase 1, Dose Escalation, and Pharmacokinetic Study of ProMetic Plasminogen Administered as Intravenous Infusion in Adults and Children With Hypoplasminogenemia
100 Clinical Results associated with Plasminogen(Omnio AB)
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100 Translational Medicine associated with Plasminogen(Omnio AB)
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100 Patents (Medical) associated with Plasminogen(Omnio AB)
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100 Deals associated with Plasminogen(Omnio AB)
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R&D Status

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IndicationHighest PhaseCountry/LocationOrganizationDate
Diabetic FootPhase 2-
Liminal BioSciences, Inc.Liminal BioSciences, Inc.
-
Diabetic FootPhase 2-
Omnio ABOmnio AB
-
Ear DiseasesPhase 2-
Liminal BioSciences, Inc.Liminal BioSciences, Inc.
-
Ear DiseasesPhase 2-
Omnio ABOmnio AB
-
Plasminogen Deficiency, Type IDiscovery
United States
ProMetic Biotherapeutics Ltd.
01 Dec 2014
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
NCT02690714 (CTgov)
Phase 2/3
Congenital Plasminogen Deficiency
15
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19 Apr 2021
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Translational Medicine

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Deal

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Core Patent

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Clinical Trial

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Approval

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Biosimilar

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Competitive landscape of biosimilars in different countries/locations. Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3.

Regulation

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