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Drug ReportsBESILESOMAB
BESILESOMAB
Scintimun (besilesomab) is an antibody pharmaceutical. Besilesomab was first approved as Scintimun on 2010-01-11. It has been approved in Europe to treat osteomyelitis and radionuclide imaging.
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Safety
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
infectionsD007239
musculoskeletal diseasesD009140
diagnosisD003933
Trade Name
FDA
EMA
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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
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Indications
FDA
EMA
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Agency Specific
FDA
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HCPCS
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Clinical
Clinical Trials
2 clinical trials
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Indications Phases 4
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Indications Phases 3
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Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Multiple myelomaD009101C90.011
Plasma cell neoplasmsD05421911
PlasmacytomaD010954C90.311
LeukemiaD007938C9511
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 nameBESILESOMAB
INNbesilesomab
Description
Besilesomab (mouse mab)
Classification
Antibody
Drug classmonoclonal antibodies
Image (chem structure or protein)Loading
Structure (InChI/SMILES or Protein Sequence)
Identifiers
PDB
CAS-ID
RxCUI
ChEMBL IDCHEMBL2108021
ChEBI ID
PubChem CID
DrugBank
UNII ID538316W9ZU (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
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Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 59 documents
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Safety
Black-box Warning
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Adverse Events
Top Adverse Reactions
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1 adverse events reported
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