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Ansuvimab
Ebanga (ansuvimab) is an antibody pharmaceutical. Ansuvimab was first approved as Ebanga on 2020-12-21.
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FDA Novel Drug Approvals 2020
Commercial
Therapeutic Areas
No data
Trade Name
FDA
EMA
Ebanga
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)
Ansuvimab
Tradename
Proper name
Company
Number
Date
Products
Ebangaansuvimab-zyklRidgeback BiotherapeuticsN-761172 RX2020-12-21
1 products
Labels
FDA
EMA
Brand Name
Status
Last Update
ebangaBiologic Licensing Application2021-01-04
Indications
FDA
EMA
No data
Agency Specific
FDA
EMA
Expiration
Code
ansuvimab, Ebanga, Ridgeback Biotherapeutics
2027-12-21Orphan excl.
Patent Expiration
No data
ATC Codes
No data
HCPCS
No data
Clinical
Clinical Trials
4 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
EbolavirusD029043111
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Ebola hemorrhagic feverD019142EFO_0007243A98.4112
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 nameANSUVIMAB
INNansuvimab
Description
Ansuvimab, sold under the brand name Ebanga, is a monoclonal antibody medication for the treatment of Zaire ebolavirus (Ebolavirus) infection.
Classification
Antibody
Drug classmonoclonal antibodies
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
Identifiers
PDB
CAS-ID
RxCUI
ChEMBL IDCHEMBL4594388
ChEBI ID
PubChem CID
DrugBankDB16385
UNII IDTG8IQ19NG2 (ChemIDplus, GSRS)
Target
Agency Approved
No data
Alternate
No data
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 109 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
Mock data
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839 adverse events reported
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