Turoctocog alfa
NovoEight (turoctocog alfa) is a protein pharmaceutical. Turoctocog alfa was first approved as Novoeight on 2013-11-13. It is used to treat factor VII deficiency, hemophilia a, hemorrhage, and von willebrand diseases in the USA. It has been approved in Europe to treat hemophilia a.
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35 clinical trials
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Indications Phases 4
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Hemophilia a | D006467 | EFO_0007267 | D66 | 9 | 1 | 12 | 1 | 12 | 35 |
| Blood coagulation disorders | D001778 | EFO_0009314 | D68.9 | 8 | — | 10 | 1 | 4 | 23 |
| Hemostatic disorders | D020141 | — | — | 8 | — | 10 | 1 | 4 | 23 |
| Hemorrhage | D006470 | MP_0001914 | R58 | — | — | 5 | 1 | — | 6 |
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Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Hemostasis | D006487 | — | — | — | 1 | — | — | — | 1 |
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
| Drug common name | Turoctocog alfa |
| INN | turoctocog alfa |
| Description | Turoctocog alfa (trade name NovoEight) is a recombinant antihemophilic factor VIII used for the treatment of and prophylaxis of bleeding patients with haemophilia A. It is marketed by Novo Nordisk. It was approved in the United States, the European Union, and Japan in 2013.
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| Classification | Protein |
| Drug class | — |
| Image (chem structure or protein) |  |
| Structure (InChI/SMILES or Protein Sequence) | — |
Identifiers
| PDB | — |
| CAS-ID | — |
| RxCUI | — |
| ChEMBL ID | CHEMBL2108286 |
| ChEBI ID | — |
| PubChem CID | — |
| DrugBank | DB09109 |
| UNII ID | 969NZA3X9T (ChemIDplus, GSRS) |
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Novoeight – Novo Nordisk
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339 adverse events reported
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