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Drug ReportsVonicog alfa
Vonicog alfa
Veyvondi (vonicog alfa) is a protein pharmaceutical. Vonicog alfa was first approved as Veyvondi on 2018-08-31. It has been approved in Europe to treat von willebrand diseases.
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
hemic and lymphatic diseasesD006425
hereditary congenital and neonatal diseases and abnormalitiesD009358
Trade Name
FDA
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Drug Products
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Clinical
Clinical Trials
26 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
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Hemophilia aD006467EFO_0007267D66113149
Indications Phases 3
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Ontology
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Von willebrand diseasesD014842EFO_0003910D68.0128112
Postpartum hemorrhageD006473O7211
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Type 3 von willebrand diseaseD056729Orphanet_166096D68.0311
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameVonicog alfa
INNvonicog alfa
Description
Vonicog alfa, sold under the brand names Vonvendi and Veyvondi, is a medication used to control bleeding in adults with von Willebrand disease (an inherited bleeding disorder). It is a recombinant von Willebrand factor.
Classification
Protein
Drug classHemostatic
Image (chem structure or protein)Loading
Structure (InChI/SMILES or Protein Sequence)
Identifiers
PDB
CAS-ID109319-16-6
RxCUI1812589
ChEMBL IDCHEMBL2107873
ChEBI ID
PubChem CID
DrugBankDB12872
UNII ID5PKM8P0G5I (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
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Trends
PubMed Central
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Additional graphs summarizing 37 documents
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Safety
Black-box Warning
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87 adverse events reported
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