Cinryze, Ruconest(conestat alfa)
Ruconest (conestat alfa) is a protein pharmaceutical. Conestat alfa was first approved as Ruconest on 2010-10-28. It has been approved in Europe to treat hereditary angioedemas.
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Commercial
Trade Name
FDA
EMA
Berinert, Cinryze, Haegarda, Ruconest
Drug Products
FDA
EMA
Reference product - 351(a)
Reference product - 351(a)
Interchangeable product - 351(k)
Interchangeable product - 351(k)
Biosimilar product - 351(k)
Biosimilar product - 351(k)
C1 esterase inhibitor (human)
Tradename | Proper name | Company | Number | Date | Products |
|---|---|---|---|---|---|
| Berinert | C1 Esterase Inhibitor (Human) | CSL Behring | A-125287 RX | 2009-10-09 | 1 products |
| Cinryze | C1 Esterase Inhibitor (Human) | Takeda | A-125267 RX | 2008-10-10 | 1 products |
C1 esterase inhibitor (recombinant)
C1 esterase inhibitor subcutaneous (human)
Tradename | Proper name | Company | Number | Date | Products |
|---|---|---|---|---|---|
| Haegarda | C1 Esterase Inhibitor Subcutaneous (Human) | CSL Behring | A-125606 RX | 2017-06-22 | 2 products |
Indications
FDA
EMA
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Agency Specific
FDA
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Patent Expiration
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Clinical
Clinical Trials
95 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 |
|---|---|---|---|---|---|---|---|---|---|
| Hereditary angioedemas | D054179 | EFO_0004131 | — | — | 6 | 4 | — | 2 | 10 |
| Angioedema | D000799 | EFO_0005532 | T78.3 | — | 4 | 4 | — | 2 | 8 |
| Inborn genetic diseases | D030342 | EFO_0000508 | — | — | 3 | 2 | — | — | 4 |
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Acute kidney injury | D058186 | — | N17 | — | 3 | — | — | — | 3 |
| Covid-19 | D000086382 | — | U07.1 | — | 2 | — | — | — | 2 |
| Kidney transplantation | D016030 | — | — | — | 1 | — | — | — | 1 |
| Graft rejection | D006084 | — | — | — | 1 | — | — | — | 1 |
| Myocardial infarction | D009203 | EFO_0000612 | I21 | — | 1 | — | — | — | 1 |
| Non-st elevated myocardial infarction | D000072658 | — | — | — | 1 | — | — | — | 1 |
| Infarction | D007238 | EFO_0009463 | — | — | 1 | — | — | — | 1 |
| Ischemic stroke | D000083242 | — | — | — | 1 | — | — | — | 1 |
| Aortic valve stenosis | D001024 | EFO_0000266 | — | — | 1 | — | — | — | 1 |
| Reperfusion injury | D015427 | — | — | — | 1 | — | — | — | 1 |
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Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Renal insufficiency | D051437 | — | N19 | 1 | — | — | — | — | 1 |
| Delayed graft function | D051799 | — | — | 1 | — | — | — | — | 1 |
Indications Without Phase
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
| Drug common name | Conestat alfa |
| INN | conestat alfa |
| Description | Ruconest (conestat alfa) is a protein pharmaceutical. Conestat alfa was first approved as Ruconest on 2010-10-28. It has been approved in Europe to treat hereditary angioedemas. |
| Classification | Protein |
| Drug class | enzyme inhibitors |
| Image (chem structure or protein) |  |
| Structure (InChI/SMILES or Protein Sequence) | — |
Identifiers
| PDB | — |
| CAS-ID | — |
| RxCUI | — |
| ChEMBL ID | CHEMBL2108350 |
| ChEBI ID | — |
| PubChem CID | — |
| DrugBank | DB06404 |
| UNII ID | 5QS67N4551 (ChemIDplus, GSRS) |
Target
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Trends
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Additional graphs summarizing 2,941 documents
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Safety
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5,433 adverse events reported
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