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Drug ReportsCIXUTUMUMAB
CIXUTUMUMAB
Cixutumumab is an antibody pharmaceutical. It is currently being investigated in clinical studies.
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Commercial
Clinical
Drug
Target
Variants
Financial
Trends
Safety
Events Timeline
5D
1M
3M
6M
YTD
1Y
2Y
5Y
Max
Events
FDA approval date
EMA approval date
Patent expiration date
Study first post date
Last update post date
Start date
Primary completion date
Completion date
Results first post date
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Commercial
No data
Clinical
Clinical Trials
43 clinical trials
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Indications Phases 4
No data
Indications Phases 3
No data
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
NeoplasmsD009369—C8061———7
Non-small-cell lung carcinomaD002289——15———5
SarcomaD012509——14———5
RhabdomyosarcomaD012208——14———5
Prostatic neoplasmsD011471—C6115———5
OsteosarcomaD012516——13———4
Synovial sarcomaD013584——13———4
Breast neoplasmsD001943EFO_0003869C5013———3
LeiomyosarcomaD007890——12———3
Hepatocellular carcinomaD006528—C22.012———3
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Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Merkel cell carcinomaD015266EFO_1001471C4A1————1
ParagangliomaD010235——1————1
Medullary carcinomaD018276——1————1
GliomaD005910EFO_0000520—1————1
Brain stem neoplasmsD020295EFO_1001767—1————1
PinealomaD010871——1————1
HemangiosarcomaD006394——1————1
Desmoplastic small round cell tumorD058405——1————1
NeurofibrosarcomaD018319——1————1
HemangiopericytomaD006393——1————1
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Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameCIXUTUMUMAB
INNcixutumumab
Description
Cixutumumab (human mab)
Classification
Antibody
Drug classmonoclonal antibodies
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Structure (InChI/SMILES or Protein Sequence)—
Identifiers
PDB—
CAS-ID—
RxCUI—
ChEMBL IDCHEMBL1743001
ChEBI ID—
PubChem CID—
DrugBank—
UNII ID2285XW22DR (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 1,149 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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115 adverse events reported
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