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Regdanvimab
Regkirona (regdanvimab) is an antibody pharmaceutical. Regdanvimab was first approved as Regkirona on 2021-11-12. It has been approved in Europe to treat dna virus infections. It is known to target spike glycoprotein.
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
infectionsD007239
Trade Name
FDA
EMA
No data
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
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Labels
FDA
EMA
No data
Indications
FDA
EMA
No data
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
No data
HCPCS
No data
Clinical
Clinical Trials
3 clinical trials
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Indications Phases 4
No data
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Covid-19D000086382U07.12113
Indications Phases 2
No data
Indications Phases 1
No data
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameREGDANVIMAB
INNregdanvimab
Description
Regdanvimab, sold under the brand name Regkirona, is a human monoclonal antibody used for the treatment of COVID-19. The antibody is directed against the spike protein of SARS-CoV-2. It is developed by Celltrion. The medicine is given by infusion (drip) into a vein.
Classification
Antibody
Drug classmonoclonal antibodies
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
Identifiers
PDB
CAS-ID2444308-95-4
RxCUI
ChEMBL IDCHEMBL4650462
ChEBI ID
PubChem CID
DrugBankDB16405
UNII IDI0BGE6P6I6 (ChemIDplus, GSRS)
Target
Agency Approved
No data
Alternate
S
S
Organism
SARS coronavirus Tor2
Gene name
S
Gene synonyms
NCBI Gene ID
Protein name
spike glycoprotein
Protein synonyms
E2, Peplomer protein
Uniprot ID
Mouse ortholog
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 340 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
0 adverse events reported
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