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Lifileucel
Lifileucel is a cell 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
29 clinical trials
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Mock data
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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
MelanomaD008545751112
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Non-small-cell lung carcinomaD002289134
Ovarian neoplasmsD010051EFO_0003893C56133
Uterine cervical neoplasmsD002583213
Squamous cell carcinoma of head and neckD00007719522
NeoplasmsD009369C80212
Fallopian tube neoplasmsD005185111
Synovial sarcomaD013584111
Skin neoplasmsD012878EFO_0004198C4411
Triple negative breast neoplasmsD06472611
Colorectal neoplasmsD01517911
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Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Uveal neoplasmsD014604EFO_100123022
Head and neck neoplasmsD00625811
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameLIFILEUCEL
INNlifileucel
Description
Lifileucel is a cell pharmaceutical. It is currently being investigated in clinical studies.
Classification
Cell
Drug class
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
Identifiers
PDB
CAS-ID
RxCUI
ChEMBL IDCHEMBL4298200
ChEBI ID
PubChem CID
DrugBank
UNII IDR0835E18NH (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 99 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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24 adverse events reported
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