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Ladiratuzumab vedotin
Ladiratuzumab vedotin is an antibody pharmaceutical. It is currently being investigated in clinical studies.
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Commercial
Therapeutic Areas
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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
EMA
No data
Patent Expiration
No data
ATC Codes
No data
HCPCS
No data
Clinical
Clinical Trials
5 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
Triple negative breast neoplasmsD064726334
Breast neoplasmsD001943EFO_0003869C50112
HemangiosarcomaD00639411
Prostatic neoplasmsD011471C6111
Non-small-cell lung carcinomaD00228911
Squamous cell carcinoma of head and neckD00007719511
MelanomaD00854511
Small cell lung carcinomaD05575211
AdenocarcinomaD00023011
Esophageal squamous cell carcinomaD00007727711
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 nameLADIRATUZUMAB VEDOTIN
INNladiratuzumab vedotin
Description
Ladiratuzumab vedotin is an antibody pharmaceutical. It is currently being investigated in clinical studies.
Classification
Antibody
Drug classsynthetic analogs of the dolastatin series; monoclonal antibodies
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
Identifiers
PDB
CAS-ID
RxCUI
ChEMBL IDCHEMBL4298101
ChEBI ID
PubChem CID
DrugBank
UNII IDVM4G5D1A60 (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 89 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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