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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
1903 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
NeoplasmsD009369—C8052—1—6
VomitingD014839—R11.1———1—1
NauseaD009325—R11.0———1—1
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Small cell lung carcinomaD055752——363——11
Lung neoplasmsD008175—C34.90263——10
Non-small-cell lung carcinomaD002289——1—2——3
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
LymphomaD008223—C85.916———6
Hodgkin diseaseD006689—C8124———5
OsteosarcomaD012516——14———4
CarcinomaD002277—C80.012———3
Prostatic neoplasmsD011471—C6121———2
Castration-resistant prostatic neoplasmsD064129——21———2
Small cell carcinomaD018288——11———2
Neuroendocrine carcinomaD018278——11———2
Large b-cell lymphoma diffuseD016403—C83.312———2
SarcomaD012509——12———2
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Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Urologic neoplasmsD014571—C64-C681————1
Urinary bladder neoplasmsD001749—C671————1
Urethral neoplasmsD014523EFO_0003846—1————1
Transitional cell carcinomaD002295——1————1
Neuroendocrine tumorsD018358EFO_1001901D3A.81————1
NeuroblastomaD009447EFO_0000621—1————1
Bone neoplasmsD001859EFO_0003820D161————1
Kidney neoplasmsD007680EFO_0003865C641————1
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name—
INN—
Description
—
Classification
Unknown
Drug class—
Image (chem structure or protein)Loading
Structure (InChI/SMILES or Protein Sequence)—
Identifiers
PDB—
CAS-ID—
RxCUI—
ChEMBL ID—
ChEBI ID—
PubChem CID—
DrugBank—
UNII ID—
Target
No data
Variants
No data
Financial
No data
Trends
No data
Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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18 adverse events reported
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