Coagulation factor x human
Coagadex (coagulation factor x human) is an unknown pharmaceutical. Coagulation factor x human was first approved as Coagadex on 2016-03-16. It has been approved in Europe to treat factor x deficiency.
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Drug Products
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New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
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Labels
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EMA
Brand Name | Status | Last Update |
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coagadex | Biologic Licensing Application | 2018-11-26 |
Indications
FDA
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Agency Specific
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Clinical
Clinical Trials
9 clinical trials
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Indications Phases 4
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Indications Phases 3
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
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Factor x deficiency | D005171 | — | — | 3 | — | 1 | 4 |
Indications Phases 2
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Indications Phases 1
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Indications Without Phase
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Atrial fibrillation | D001281 | EFO_0000275 | I48.0 | — | — | — | — | 1 | 1 |
Venous thromboembolism | D054556 | EFO_0004286 | I74 | — | — | — | — | 1 | 1 |
Liver cirrhosis | D008103 | EFO_0001422 | K74.0 | — | — | — | — | 1 | 1 |
Coagulation protein disorders | D020147 | — | — | — | — | 1 | 1 | ||
Depression | D003863 | F33.9 | — | — | — | — | 1 | 1 | |
Emotional regulation | D000080103 | — | — | — | — | 1 | 1 |
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | COAGULATION FACTOR X HUMAN |
INN | — |
Description | Factor X, also known by the eponym Stuart–Prower factor, is an enzyme (EC 3.4.21.6) of the coagulation cascade. It is a serine endopeptidase (protease group S1, PA clan). Factor X is synthesized in the liver and requires vitamin K for its synthesis.
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Classification | Unknown |
Drug class | — |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | — |
Identifiers
PDB | — |
CAS-ID | — |
RxCUI | — |
ChEMBL ID | CHEMBL4297951 |
ChEBI ID | — |
PubChem CID | — |
DrugBank | — |
UNII ID | — |
Target
Agency Approved
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Variants
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Trends
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Additional graphs summarizing 18 documents
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Safety
Black-box Warning
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Adverse Events
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30,049 adverse events reported
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