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Drug ReportsCatridecacog
Catridecacog
NovoThirteen (catridecacog) is a protein pharmaceutical. Catridecacog was first approved as Novothirteen on 2012-09-03. It has been approved in Europe to treat inherited blood coagulation disorders.
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
hemic and lymphatic diseasesD006425
hereditary congenital and neonatal diseases and abnormalitiesD009358
Trade Name
FDA
EMA
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Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
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Labels
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Indications
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EMA
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Ontology
MeSH
ICD-10
inherited blood coagulation disordersD025861
Agency Specific
FDA
EMA
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Patent Expiration
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ATC Codes
B: Blood and blood forming organ drugs
B02: Antihemorrhagics
B02B: Vitamin k and other hemostatics
B02BD: Blood coagulation factors
B02BD11: Catridecacog
HCPCS
No data
Clinical
Clinical Trials
14 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
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Total
Blood coagulation disordersD001778EFO_0009314D68.9614213
Hemostatic disordersD020141614213
Factor xiii deficiencyD00517711
HemorrhageD006470MP_0001914R5811
Indications Phases 2
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MeSH
Ontology
ICD-10
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Ph 3
Ph 4
Other
Total
Cardiac surgical proceduresD006348213
Ulcerative colitisD003093EFO_0000729K5111
InflammationD007249MP_000184511
ColitisD003092EFO_0003872K52.911
UlcerD014456MPATH_57911
Indications Phases 1
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MeSH
Ontology
ICD-10
Ph 1
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Total
Healthy volunteers/patients44
Indications Without Phase
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameCatridecacog
INNcatridecacog
Description
Catridecacog, sold under the brand name Tretten in the US and NovoThirteen in the EU) is a class of recombinant factor XIII A-subunit based biopharmaceutical medicine, indicated in patients with a rare clotting disorder, congenital factor XIII A-subunit deficiency, which is a kind of Factor XIII deficiency. The medication prevents bleeding in patients with this condition, and has been approved by the U.S. Food and Drug Administration (FDA) for this use in the US in 2014. It was brought to market by Novo Nordisk.
Classification
Protein
Drug class
Image (chem structure or protein)Loading
Structure (InChI/SMILES or Protein Sequence)
Identifiers
PDB
CAS-ID
RxCUI
ChEMBL IDCHEMBL2108282
ChEBI ID
PubChem CID
DrugBankDB09310
UNII IDNU23Q531G1 (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 79 documents
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Safety
Black-box Warning
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Adverse Events
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14 adverse events reported
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