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Elezanumab
Elezanumab is an antibody pharmaceutical. It is currently being investigated in clinical studies. The pharmaceutical is active against repulsive guidance molecule A.
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Commercial
Therapeutic Areas
No data
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)
No data
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
7 clinical trials
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Indications Phases 4
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Indications Phases 3
No data
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Multiple sclerosisD009103EFO_0003885G35224
Ischemic strokeD000083242112
Spinal cord injuriesD013119EFO_100191911
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 nameELEZANUMAB
INNelezanumab
Description
Elezanumab is an antibody pharmaceutical. It is currently being investigated in clinical studies. The pharmaceutical is active against repulsive guidance molecule A.
Classification
Antibody
Drug classmonoclonal antibodies
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
Identifiers
PDB
CAS-ID
RxCUI
ChEMBL IDCHEMBL4297743
ChEBI ID
PubChem CID
DrugBank
UNII IDSK1LVT23A1 (ChemIDplus, GSRS)
Target
Agency Approved
RGMA
RGMA
Organism
Homo sapiens
Gene name
RGMA
Gene synonyms
RGM
NCBI Gene ID
Protein name
repulsive guidance molecule A
Protein synonyms
repulsive guidance molecule family member a, RGM domain family member A, RGM domain family, member A
Uniprot ID
Mouse ortholog
Rgma (244058)
repulsive guidance molecule A (Q8CIH6)
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 27 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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2 adverse events reported
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