Vonvendi, Veyvondi(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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Vonvendi
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Reference product - 351(a)
Reference product - 351(a)
Interchangeable product - 351(k)
Interchangeable product - 351(k)
Biosimilar product - 351(k)
Biosimilar product - 351(k)
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31 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 |
|---|---|---|---|---|---|---|---|---|---|
| Von willebrand diseases | D014842 | EFO_0003910 | D68.0 | 1 | — | 4 | — | — | 5 |
Indications Phases 2
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Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Type 3 von willebrand disease | D056729 | Orphanet_166096 | D68.03 | 1 | — | — | — | — | 1 |
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Epidemiology
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Drug
General
| Drug common name | Vonicog alfa |
| INN | vonicog 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.
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| Classification | Protein |
| Drug class | Hemostatic |
| Image (chem structure or protein) |  |
| Structure (InChI/SMILES or Protein Sequence) | — |
Identifiers
| PDB | — |
| CAS-ID | 109319-16-6 |
| RxCUI | 1812589 |
| ChEMBL ID | CHEMBL2107873 |
| ChEBI ID | — |
| PubChem CID | — |
| DrugBank | DB12872 |
| UNII ID | 5PKM8P0G5I (ChemIDplus, GSRS) |
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Vonvendi – Takeda
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398 adverse events reported
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