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Drug ReportsVUDALIMAB
VUDALIMAB
Vudalimab 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
9 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
CarcinomaD002277—C80.013———4
Castration-resistant prostatic neoplasmsD064129——12———3
Uterine cervical neoplasmsD002583HP_0030159—12———3
Prostatic neoplasmsD011471—C6112———3
Colorectal neoplasmsD015179——11———2
Ovarian neoplasmsD010051EFO_0003893C5611———2
Non-small-cell lung carcinomaD002289——21———2
Endometrial neoplasmsD016889EFO_0004230—11———2
Lung neoplasmsD008175HP_0100526C34.9021———2
Small cell lung carcinomaD055752——11———2
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Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Renal cell carcinomaD002292EFO_0000376—1————1
Urologic neoplasmsD014571—C64-C681————1
Breast neoplasmsD001943EFO_0003869C501————1
NeoplasmsD009369—C801————1
Hepatocellular carcinomaD006528—C22.01————1
Nasopharyngeal carcinomaD000077274——1————1
Basal cell carcinomaD002280——1————1
Fallopian tube neoplasmsD005185——1————1
Squamous cell carcinoma of head and neckD000077195——1————1
MelanomaD008545——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 nameVUDALIMAB
INNvudalimab
Description
Vudalimab is an antibody pharmaceutical. It is currently being investigated in clinical studies.
Classification
Antibody
Drug classmonoclonal antibodies
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Structure (InChI/SMILES or Protein Sequence)—
Identifiers
PDB—
CAS-ID—
RxCUI—
ChEMBL IDCHEMBL4594617
ChEBI ID—
PubChem CID—
DrugBank—
UNII ID4I9I5X3Z6N (ChemIDplus, GSRS)
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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15 adverse events reported
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