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Ublituximab
Briumvi (ublituximab) is an antibody pharmaceutical. Ublituximab was first approved as Briumvi on 2022-12-28. It is used to treat relapsing-remitting multiple sclerosis in the USA. The pharmaceutical is active against B-lymphocyte antigen CD20.
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
nervous system diseasesD009422
immune system diseasesD007154
Trade Name
FDA
EMA
Briumvi
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)
Ublituximab
Tradename
Proper name
Company
Number
Date
Products
Briumviublituximab-xiiyTG TherapeuticsN-761238 RX2022-12-28
1 products
Labels
FDA
EMA
Brand Name
Status
Last Update
briumviBiologic Licensing Application2023-01-03
Indications
FDA
EMA
Indication
Ontology
MeSH
ICD-10
relapsing-remitting multiple sclerosisEFO_0003929D020529
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
No data
HCPCS
No data
Clinical
Clinical Trials
32 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
B-cell chronic lymphocytic leukemiaD015451C91.1712417
Follicular lymphomaD008224C823416
Mantle-cell lymphomaD020522C83.14516
Multiple sclerosisD009103EFO_0003885G35134
Large b-cell lymphoma diffuseD016403C83.3111
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Non-hodgkin lymphomaD008228C85.9647
Waldenstrom macroglobulinemiaD008258C88.0323
B-cell lymphomaD016393323
Relapsing-remitting multiple sclerosisD020529EFO_000392911
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
B-cell lymphoma marginal zoneD018442C88.411
Neuromyelitis opticaD009471EFO_0004256G36.011
Reactive arthritisD016918EFO_0007460M02.311
Hodgkin diseaseD006689C8111
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameUBLITUXIMAB
INNublituximab
Description
Ublituximab, sold under the brand name Briumvi, is an immunomodulator used for the treatment of multiple sclerosis. It is a CD20-directed cytolytic monoclonal antibody.
Classification
Antibody
Drug classmonoclonal antibodies
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
Identifiers
PDB
CAS-ID1174014-05-1
RxCUI
ChEMBL IDCHEMBL2108354
ChEBI ID
PubChem CID
DrugBankDB11850
UNII IDU59UGK3IPC (ChemIDplus, GSRS)
Target
Agency Approved
MS4A1
MS4A1
Organism
Homo sapiens
Gene name
MS4A1
Gene synonyms
CD20
NCBI Gene ID
Protein name
B-lymphocyte antigen CD20
Protein synonyms
B-lymphocyte cell-surface antigen B1, B-lymphocyte surface antigen B1, Bp35, CD20, CD20 antigen, CD20 receptor, Leukocyte surface antigen Leu-16, Membrane-spanning 4-domains subfamily A member 1, membrane-spanning 4-domains, subfamily A, member 1
Uniprot ID
Mouse ortholog
Ms4a1 (12482)
B-lymphocyte antigen CD20 (P19437)
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 400 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
Mock data
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45 adverse events reported
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