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Ganitumab
Ganitumab is an antibody pharmaceutical. It is currently being investigated in clinical studies.
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Commercial
Therapeutic Areas
No data
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)
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
30 clinical trials
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Mock data
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Indications Phases 4
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Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
NeoplasmsD009369C80552——9
Pancreatic neoplasmsD010190EFO_0003860C25551——7
Ewing sarcomaD012512EFO_0000173—21—14
Neoplasm metastasisD009362EFO_00097081—1——2
Bone neoplasmsD001859EFO_0003820D16——1——1
Primitive neuroectodermal tumors peripheralD018241——1——1
Neuroectodermal tumorsD017599——1——1
Cancer painD000072716G89.3——1——1
Endocrine gland neoplasmsD004701EFO_0003769D35——1——1
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Colorectal neoplasmsD01517925———5
SarcomaD01250933———5
Non-small-cell lung carcinomaD00228933———4
Breast neoplasmsD001943EFO_0003869C5013———3
Ovarian neoplasmsD010051EFO_0003893C5613———3
LymphomaD008223C85.911———2
Carcinoid tumorD002276D3A.00—2———2
Triple negative breast neoplasmsD064726—1———1
HemangiosarcomaD006394—1———1
RhabdomyosarcomaD01220811———1
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Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Prostatic neoplasmsD011471C611————1
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameGANITUMAB
INNganitumab
Description
Ganitumab (human mab)
Classification
Antibody
Drug classmonoclonal antibodies
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)—
Identifiers
PDB—
CAS-ID905703-97-1
RxCUI—
ChEMBL IDCHEMBL1743024
ChEBI ID—
PubChem CID—
DrugBankDB12205
UNII IDCK1441RCZ8 (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 659 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
Mock data
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22 adverse events reported
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