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Drug ReportsConestat alfa
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
Therapeutic Areas
Therapeutic Area
MeSH
cardiovascular diseasesD002318
hereditary congenital and neonatal diseases and abnormalitiesD009358
skin and connective tissue diseasesD017437
immune system diseasesD007154
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
BerinertC1 Esterase Inhibitor (Human)CSL BehringA-125287 RX2009-10-09
1 products
CinryzeC1 Esterase Inhibitor (Human)TakedaA-125267 RX2008-10-10
1 products
C1 esterase inhibitor (recombinant)
Tradename
Proper name
Company
Number
Date
Products
RuconestC1 Esterase Inhibitor (Recombinant)PharmingA-125495 RX2014-07-16
1 products
C1 esterase inhibitor subcutaneous (human)
Tradename
Proper name
Company
Number
Date
Products
HaegardaC1 Esterase Inhibitor Subcutaneous (Human)CSL BehringA-125606 RX2017-06-22
2 products
Labels
FDA
EMA
Brand Name
Status
Last Update
berinertBiologic Licensing Application2009-11-10
cinryzeBiologic Licensing Application2010-11-01
ruconestBiologic Licensing Application2020-04-30
Indications
FDA
EMA
No data
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
B: Blood and blood forming organ drugs
— B06: Other hematological agents in atc
— B06A: Other hematological agents in atc
— B06AC: Drugs used in hereditary angioedema
— B06AC04: Conestat alfa
HCPCS
No data
Clinical
Clinical Trials
94 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Hereditary angioedemasD054179EFO_0004131—6192251460
AngioedemaD000799EFO_0005532T78.34131621342
Hereditary angioedema types i and iiD056829——242119
Inborn genetic diseasesD030342EFO_0000508——431—6
Drug-related side effects and adverse reactionsD064420—T88.7———1—1
Primary immunodeficiency diseasesD000081207—————1—1
Common variable immunodeficiencyD017074EFO_0000367D83———1—1
AsthmaD001249EFO_0000270J45———1—1
Rare diseasesD035583—————1—1
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
InflammationD007249MP_0001845——12—14
SepsisD018805EFO_0001420A41.9——2—13
Wounds and injuriesD014947—T14.8—11——2
EndotoxemiaD019446————1—12
Multiple organ failureD009102EFO_1001373———1—12
Innate immunityD007113————1——1
Immune system diseasesD007154—D89.9—11——1
HypersensitivityD006967EFO_0003785T78.40—11——1
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Covid-19D000086382—U07.1—4———4
Reperfusion injuryD015427——13———3
Renal insufficiencyD051437—N1931———3
Kidney transplantationD016030——13———3
Acute kidney injuryD058186—N17—3———3
Chronic renal insufficiencyD051436—N1822———2
Chronic kidney failureD007676EFO_0003884N18.622———2
Delayed graft functionD051799——21———2
Graft rejectionD006084———2———2
Ischemic strokeD000083242——11———2
Show 33 more
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Neuromyelitis opticaD009471EFO_0004256G36.01————1
Cardiovascular diseasesD002318EFO_0000319I981————1
StrokeD020521EFO_0000712I63.91————1
Cerebrovascular disordersD002561EFO_0003763I60-I691————1
IschemiaD007511EFO_0000556—1————1
Vascular diseasesD014652EFO_0004264I771————1
Cerebral infarctionD002544—I631————1
Brain infarctionD020520EFO_0004277I631————1
Brain ischemiaD002545EFO_0003883I67.821————1
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Immunologic testsD007159——————11
Graft vs host diseaseD006086—D89.81————11
Systemic mastocytosisD034721—C96.21————11
UrticariaD014581EFO_0005531L50————11
MastocytosisD008415—D47.09————11
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameConestat alfa
INNconestat 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 classenzyme inhibitors
Image (chem structure or protein)Loading
Structure (InChI/SMILES or Protein Sequence)—
Identifiers
PDB—
CAS-ID—
RxCUI—
ChEMBL IDCHEMBL2108350
ChEBI ID—
PubChem CID—
DrugBankDB06404
UNII ID5QS67N4551 (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
Revenue by drug
$
€
£
â‚£
Ruconest – Pharming
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Cinryze – Shire
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Cinryze – Takeda
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Tabular view
Estimated US medical usage
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 2,911 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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5,433 adverse events reported
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