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Serplulimab
Serplulimab 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
No data
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
54 clinical trials
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Indications Phases 4
No data
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
NeoplasmsD009369C80516
Non-small-cell lung carcinomaD0022891325
Uterine cervical neoplasmsD002583213
Colorectal neoplasmsD015179212
Hepatocellular carcinomaD006528C22.0112
Esophageal squamous cell carcinomaD000077277112
Stomach neoplasmsD013274EFO_0003897C16112
Triple negative breast neoplasmsD06472611
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Liver neoplasmsD008113EFO_1001513C22.022
Squamous cell carcinoma of head and neckD00007719511
Small cell lung carcinomaD05575211
Adenocarcinoma of lungD00007719211
Neoadjuvant therapyD02036011
Neuroendocrine carcinomaD018278111
Nasopharyngeal carcinomaD00007727411
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 nameSERPLULIMAB
INNserplulimab
Description
Serplulimab is an antibody pharmaceutical. It is currently being investigated in clinical studies.
Classification
Antibody
Drug classmonoclonal antibodies
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
Identifiers
PDB
CAS-ID
RxCUI
ChEMBL IDCHEMBL4594550
ChEBI ID
PubChem CID
DrugBank
UNII IDS3GQZ2K36V (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 58 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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57 adverse events reported
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