Urokinase
Kinlytic (urokinase) is an enzyme pharmaceutical. Urokinase was first approved as Kinlytic on 1978-01-16. It is used to treat coronary thrombosis, myocardial infarction, pulmonary embolism, vascular graft occlusion, and venous thrombosis in the USA.
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EMA
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Drug Products
FDA
EMA
Reference product - 351(a)
Reference product - 351(a)
Interchangeable product - 351(k)
Interchangeable product - 351(k)
Biosimilar product - 351(k)
Biosimilar product - 351(k)
Urokinase
Tradename | Proper name | Company | Number | Date | Products |
---|---|---|---|---|---|
Kinlytic | urokinase | Microbix Biosystems | N-21846 DISCN | 1978-01-16 | 3 products |
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Indications
FDA
EMA
Indication | Ontology | MeSH | ICD-10 |
---|---|---|---|
coronary thrombosis | EFO_1000883 | D003328 | I21 |
myocardial infarction | EFO_0000612 | D009203 | I21 |
pulmonary embolism | EFO_0003827 | D011655 | I26 |
vascular graft occlusion | — | D006083 | — |
venous thrombosis | HP_0004936 | D020246 | I82.40 |
Agency Specific
FDA
EMA
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Patent Expiration
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Clinical
Indications Phases 4
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Indications Phases 3
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Indications Phases 2
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Indications Phases 1
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Indications Without Phase
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | UROKINASE |
INN | urokinase |
Description | Urokinase-type plasminogen activator precursor (uPA) (U-plasminogen activator) |
Classification | Enzyme |
Drug class | enzymes |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | >1C5N:H|Thrombin heavy chain
IVEGSDAEIGMSPWQVMLFRKSPQELLCGASLISDRWVLTAAHCLLYPPWDKNFTENDLLVRIGKHSRTRYERNIEKISM
LEKIYIHPRYNWRENLDRDIALMKLKKPVAFSDYIHPVCLPDRETAASLLQAGYKGRVTGWGNLKETWTANVGKGQPSVL
QVVNLPIVERPVCKDSTRIRITDNMFCAGYKPDEGKRGDACEGDSGGPFVMKSPFNNRWYQMGIVSWGEGCDRDGKYGFY
THVFRLKKWIQKVIDQFGE
>1C5N:L|Thrombin light chain
TFGSGEADCGLRPLFEKKSLEDKTERELLESYIDGR |
Identifiers
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Alternate
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Variants
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Safety
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1 adverse events reported
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